--- _id: '10282' abstract: - lang: eng text: Advanced transcriptome sequencing has revealed that the majority of eukaryotic genes undergo alternative splicing (AS). Nonetheless, little effort has been dedicated to investigating the functional relevance of particular splicing events, even those in the key developmental and hormonal regulators. Combining approaches of genetics, biochemistry and advanced confocal microscopy, we describe the impact of alternative splicing on the PIN7 gene in the model plant Arabidopsis thaliana. PIN7 encodes a polarly localized transporter for the phytohormone auxin and produces two evolutionarily conserved transcripts, PIN7a and PIN7b. PIN7a and PIN7b, differing in a four amino acid stretch, exhibit almost identical expression patterns and subcellular localization. We reveal that they are closely associated and mutually influence each other's mobility within the plasma membrane. Phenotypic complementation tests indicate that the functional contribution of PIN7b per se is minor, but it markedly reduces the prominent PIN7a activity, which is required for correct seedling apical hook formation and auxin-mediated tropic responses. Our results establish alternative splicing of the PIN family as a conserved, functionally relevant mechanism, revealing an additional regulatory level of auxin-mediated plant development. acknowledgement: We thank Claus Schwechheimer for the pin34 and pin347 seeds, Yuliia Mironova for technical assistance, Ksenia Timofeyenko and Dmitry Konovalov for help with the evolutional analysis, Konstantin Kutashev and Siarhei Dabravolski for assistance with FRET-FLIM, Huibin Han for advice with hypocotyl imaging, Karel Müller for the initial qRT-PCR on the tobacco cell lines, Stano Pekár for suggestions regarding the statistical analysis of the morphodynamic measurements, and Jozef Mravec, Dolf Weijers and Lindy Abas for their comments on the manuscript. This work was supported by the Czech Science Foundation (projects 16-26428S and 19-23773S to IK, MH and KRůžička, 19-18917S to JHumpolíčková and 18-26981S to JF), and the Ministry of Education, Youth and Sports of the Czech Republic (MEYS, CZ.02.1.01/0.0/0.0/16_019/0000738) to KRůžička and JHejátko. The imaging facilities of the Institute of Experimental Botany and CEITEC are supported by MEYS (LM2018129 – Czech BioImaging and CZ.02.1.01/0.0/0.0/16_013/0001775). The authors declare no competing interests. article_processing_charge: No article_type: original author: - first_name: Ivan full_name: Kashkan, Ivan last_name: Kashkan - first_name: Mónika full_name: Hrtyan, Mónika id: 45A71A74-F248-11E8-B48F-1D18A9856A87 last_name: Hrtyan - first_name: Katarzyna full_name: Retzer, Katarzyna last_name: Retzer - first_name: Jana full_name: Humpolíčková, Jana last_name: Humpolíčková - first_name: Aswathy full_name: Jayasree, Aswathy last_name: Jayasree - first_name: Roberta full_name: Filepová, Roberta last_name: Filepová - first_name: Zuzana full_name: Vondráková, Zuzana last_name: Vondráková - first_name: Sibu full_name: Simon, Sibu id: 4542EF9A-F248-11E8-B48F-1D18A9856A87 last_name: Simon orcid: 0000-0002-1998-6741 - first_name: Debbie full_name: Rombaut, Debbie last_name: Rombaut - first_name: Thomas B. full_name: Jacobs, Thomas B. last_name: Jacobs - first_name: Mikko J. full_name: Frilander, Mikko J. last_name: Frilander - first_name: Jan full_name: Hejátko, Jan last_name: Hejátko - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Kamil full_name: Růžička, Kamil last_name: Růžička citation: ama: Kashkan I, Hrtyan M, Retzer K, et al. Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana. New Phytologist. 2021;233:329-343. doi:10.1111/nph.17792 apa: Kashkan, I., Hrtyan, M., Retzer, K., Humpolíčková, J., Jayasree, A., Filepová, R., … Růžička, K. (2021). Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana. New Phytologist. Wiley. https://doi.org/10.1111/nph.17792 chicago: Kashkan, Ivan, Mónika Hrtyan, Katarzyna Retzer, Jana Humpolíčková, Aswathy Jayasree, Roberta Filepová, Zuzana Vondráková, et al. “Mutually Opposing Activity of PIN7 Splicing Isoforms Is Required for Auxin-Mediated Tropic Responses in Arabidopsis Thaliana.” New Phytologist. Wiley, 2021. https://doi.org/10.1111/nph.17792. ieee: I. Kashkan et al., “Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana,” New Phytologist, vol. 233. Wiley, pp. 329–343, 2021. ista: Kashkan I, Hrtyan M, Retzer K, Humpolíčková J, Jayasree A, Filepová R, Vondráková Z, Simon S, Rombaut D, Jacobs TB, Frilander MJ, Hejátko J, Friml J, Petrášek J, Růžička K. 2021. Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana. New Phytologist. 233, 329–343. mla: Kashkan, Ivan, et al. “Mutually Opposing Activity of PIN7 Splicing Isoforms Is Required for Auxin-Mediated Tropic Responses in Arabidopsis Thaliana.” New Phytologist, vol. 233, Wiley, 2021, pp. 329–43, doi:10.1111/nph.17792. short: I. Kashkan, M. Hrtyan, K. Retzer, J. Humpolíčková, A. Jayasree, R. Filepová, Z. Vondráková, S. Simon, D. Rombaut, T.B. Jacobs, M.J. Frilander, J. Hejátko, J. Friml, J. Petrášek, K. Růžička, New Phytologist 233 (2021) 329–343. date_created: 2021-11-14T23:01:24Z date_published: 2021-11-05T00:00:00Z date_updated: 2023-08-14T11:46:43Z day: '05' department: - _id: JiFr doi: 10.1111/nph.17792 external_id: isi: - '000714678100001' pmid: - '34637542' intvolume: ' 233' isi: 1 language: - iso: eng main_file_link: - open_access: '1' url: https://www.biorxiv.org/content/10.1101/2020.05.02.074070v2 month: '11' oa: 1 oa_version: Preprint page: 329-343 pmid: 1 publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646X publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 233 year: '2021' ... --- _id: '10326' abstract: - lang: eng text: Strigolactones (SLs) are carotenoid-derived plant hormones that control shoot branching and communications between host plants and symbiotic fungi or root parasitic plants. Extensive studies have identified the key components participating in SL biosynthesis and signalling, whereas the catabolism or deactivation of endogenous SLs in planta remains largely unknown. Here, we report that the Arabidopsis carboxylesterase 15 (AtCXE15) and its orthologues function as efficient hydrolases of SLs. We show that overexpression of AtCXE15 promotes shoot branching by dampening SL-inhibited axillary bud outgrowth. We further demonstrate that AtCXE15 could bind and efficiently hydrolyse SLs both in vitro and in planta. We also provide evidence that AtCXE15 is capable of catalysing hydrolysis of diverse SL analogues and that such CXE15-dependent catabolism of SLs is evolutionarily conserved in seed plants. These results disclose a catalytic mechanism underlying homoeostatic regulation of SLs in plants, which also provides a rational approach to spatial-temporally manipulate the endogenous SLs and thus architecture of crops and ornamental plants. acknowledgement: We thank J. Li (Institute of Genetics and Developmental Biology, China) for providing the at14-1, atmax2-1, atmax3-9, atmax4-1, atmax1-1, kai2-2 (Col-0 background) mutants and B. Xu for providing the complementary DNA of P. patens. We are grateful to L. Wang for assistance with MST, B. Han for assistance with UPLC–MS, J. Li for assistance with confocal microscopy and B. Mikael and J. Zhang for their comments on the manuscript. This work was supported by grants from Strategic Priority Research Program of Chinese Academy of Sciences (Y.H., XDB27030102) and the National Natural Science Foundation of China (E.X., 31700253; Y.H., 31830055). article_processing_charge: No article_type: original author: - first_name: Enjun full_name: Xu, Enjun last_name: Xu - first_name: Liang full_name: Chai, Liang last_name: Chai - first_name: Shiqi full_name: Zhang, Shiqi last_name: Zhang - first_name: Ruixue full_name: Yu, Ruixue last_name: Yu - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Chongyi full_name: Xu, Chongyi last_name: Xu - first_name: Yuxin full_name: Hu, Yuxin last_name: Hu citation: ama: Xu E, Chai L, Zhang S, et al. Catabolism of strigolactones by a carboxylesterase. Nature Plants. 2021;7:1495–1504. doi:10.1038/s41477-021-01011-y apa: Xu, E., Chai, L., Zhang, S., Yu, R., Zhang, X., Xu, C., & Hu, Y. (2021). Catabolism of strigolactones by a carboxylesterase. Nature Plants. Springer Nature. https://doi.org/10.1038/s41477-021-01011-y chicago: Xu, Enjun, Liang Chai, Shiqi Zhang, Ruixue Yu, Xixi Zhang, Chongyi Xu, and Yuxin Hu. “Catabolism of Strigolactones by a Carboxylesterase.” Nature Plants. Springer Nature, 2021. https://doi.org/10.1038/s41477-021-01011-y. ieee: E. Xu et al., “Catabolism of strigolactones by a carboxylesterase,” Nature Plants, vol. 7. Springer Nature, pp. 1495–1504, 2021. ista: Xu E, Chai L, Zhang S, Yu R, Zhang X, Xu C, Hu Y. 2021. Catabolism of strigolactones by a carboxylesterase. Nature Plants. 7, 1495–1504. mla: Xu, Enjun, et al. “Catabolism of Strigolactones by a Carboxylesterase.” Nature Plants, vol. 7, Springer Nature, 2021, pp. 1495–1504, doi:10.1038/s41477-021-01011-y. short: E. Xu, L. Chai, S. Zhang, R. Yu, X. Zhang, C. Xu, Y. Hu, Nature Plants 7 (2021) 1495–1504. date_created: 2021-11-21T23:01:30Z date_published: 2021-11-11T00:00:00Z date_updated: 2023-08-14T11:54:02Z day: '11' department: - _id: JiFr doi: 10.1038/s41477-021-01011-y external_id: isi: - '000717408000002' pmid: - '34764442' intvolume: ' 7' isi: 1 language: - iso: eng month: '11' oa_version: None page: '1495–1504 ' pmid: 1 publication: Nature Plants publication_identifier: eissn: - 2055-0278 publication_status: published publisher: Springer Nature quality_controlled: '1' scopus_import: '1' status: public title: Catabolism of strigolactones by a carboxylesterase type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 7 year: '2021' ... --- _id: '9368' abstract: - lang: eng text: The quality control system for messenger RNA (mRNA) is fundamental for cellular activities in eukaryotes. To elucidate the molecular mechanism of 3'-Phosphoinositide-Dependent Protein Kinase1 (PDK1), a master regulator that is essential throughout eukaryotic growth and development, we employed a forward genetic approach to screen for suppressors of the loss-of-function T-DNA insertion double mutant pdk1.1 pdk1.2 in Arabidopsis thaliana. Notably, the severe growth attenuation of pdk1.1 pdk1.2 was rescued by sop21 (suppressor of pdk1.1 pdk1.2), which harbours a loss-of-function mutation in PELOTA1 (PEL1). PEL1 is a homologue of mammalian PELOTA and yeast (Saccharomyces cerevisiae) DOM34p, which each form a heterodimeric complex with the GTPase HBS1 (HSP70 SUBFAMILY B SUPPRESSOR1, also called SUPERKILLER PROTEIN7, SKI7), a protein that is responsible for ribosomal rescue and thereby assures the quality and fidelity of mRNA molecules during translation. Genetic analysis further revealed that a dysfunctional PEL1-HBS1 complex failed to degrade the T-DNA-disrupted PDK1 transcripts, which were truncated but functional, and thus rescued the growth and developmental defects of pdk1.1 pdk1.2. Our studies demonstrated the functionality of a homologous PELOTA-HBS1 complex and identified its essential regulatory role in plants, providing insights into the mechanism of mRNA quality control. acknowledgement: 'We gratefully acknowledge the Arabidopsis Biological Resource Centre (ABRC) for providing T-DNA insertional mutants, and Prof. Remko Offringa for sharing published seeds. We thank Yuchuan Liu (Shanghai OE Biotech Co., Ltd) for help with proteomics data analysis, Xixi Zhang (IST Austria) for providing the pDONR-P4P1r-mCherry plasmid, and Yao Xiao (Technical University of Munich), Alexander Johnson (IST Austria) and Hana Semeradova (IST Austria) for helpful discussions. The study was supported by National Natural Science Foundation of China (NSFC, 31721001, 91954206, to H.-W. X.), “Ten-Thousand Talent Program” (to H.-W. X.) and Collaborative Innovation Center of Crop Stress Biology, Henan Province, and Austrian Science Fund (FWF): I 3630-B25 (to J. F.). S.T. was funded by a European Molecular Biology Organization (EMBO) long-term postdoctoral fellowship (ALTF 723-2015).' article_processing_charge: No article_type: original author: - first_name: W full_name: Kong, W last_name: Kong - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Q full_name: Zhao, Q last_name: Zhao - first_name: DL full_name: Lin, DL last_name: Lin - first_name: ZH full_name: Xu, ZH last_name: Xu - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: HW full_name: Xue, HW last_name: Xue citation: ama: Kong W, Tan S, Zhao Q, et al. mRNA surveillance complex PELOTA-HBS1 eegulates phosphoinositide-sependent protein kinase1 and plant growth. Plant Physiology. 2021;186(4):2003-2020. doi:10.1093/plphys/kiab199 apa: Kong, W., Tan, S., Zhao, Q., Lin, D., Xu, Z., Friml, J., & Xue, H. (2021). mRNA surveillance complex PELOTA-HBS1 eegulates phosphoinositide-sependent protein kinase1 and plant growth. Plant Physiology. American Society of Plant Biologists. https://doi.org/10.1093/plphys/kiab199 chicago: Kong, W, Shutang Tan, Q Zhao, DL Lin, ZH Xu, Jiří Friml, and HW Xue. “MRNA Surveillance Complex PELOTA-HBS1 Eegulates Phosphoinositide-Sependent Protein Kinase1 and Plant Growth.” Plant Physiology. American Society of Plant Biologists, 2021. https://doi.org/10.1093/plphys/kiab199. ieee: W. Kong et al., “mRNA surveillance complex PELOTA-HBS1 eegulates phosphoinositide-sependent protein kinase1 and plant growth,” Plant Physiology, vol. 186, no. 4. American Society of Plant Biologists, pp. 2003–2020, 2021. ista: Kong W, Tan S, Zhao Q, Lin D, Xu Z, Friml J, Xue H. 2021. mRNA surveillance complex PELOTA-HBS1 eegulates phosphoinositide-sependent protein kinase1 and plant growth. Plant Physiology. 186(4), 2003–2020. mla: Kong, W., et al. “MRNA Surveillance Complex PELOTA-HBS1 Eegulates Phosphoinositide-Sependent Protein Kinase1 and Plant Growth.” Plant Physiology, vol. 186, no. 4, American Society of Plant Biologists, 2021, pp. 2003–20, doi:10.1093/plphys/kiab199. short: W. Kong, S. Tan, Q. Zhao, D. Lin, Z. Xu, J. Friml, H. Xue, Plant Physiology 186 (2021) 2003–2020. date_created: 2021-05-03T13:28:20Z date_published: 2021-04-30T00:00:00Z date_updated: 2023-09-05T12:20:27Z day: '30' department: - _id: JiFr doi: 10.1093/plphys/kiab199 external_id: isi: - '000703922000025' pmid: - '33930167' intvolume: ' 186' isi: 1 issue: '4' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1093/plphys/kiab199 month: '04' oa: 1 oa_version: Published Version page: 2003-2020 pmid: 1 project: - _id: 256FEF10-B435-11E9-9278-68D0E5697425 grant_number: 723-2015 name: Long Term Fellowship - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: American Society of Plant Biologists quality_controlled: '1' status: public title: mRNA surveillance complex PELOTA-HBS1 eegulates phosphoinositide-sependent protein kinase1 and plant growth tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 186 year: '2021' ... --- _id: '9290' abstract: - lang: eng text: Polar subcellular localization of the PIN exporters of the phytohormone auxin is a key determinant of directional, intercellular auxin transport and thus a central topic of both plant cell and developmental biology. Arabidopsis mutants lacking PID, a kinase that phosphorylates PINs, or the MAB4/MEL proteins of unknown molecular function display PIN polarity defects and phenocopy pin mutants, but mechanistic insights into how these factors convey PIN polarity are missing. Here, by combining protein biochemistry with quantitative live-cell imaging, we demonstrate that PINs, MAB4/MELs, and AGC kinases interact in the same complex at the plasma membrane. MAB4/MELs are recruited to the plasma membrane by the PINs and in concert with the AGC kinases maintain PIN polarity through limiting lateral diffusion-based escape of PINs from the polar domain. The PIN-MAB4/MEL-PID protein complex has self-reinforcing properties thanks to positive feedback between AGC kinase-mediated PIN phosphorylation and MAB4/MEL recruitment. We thus uncover the molecular mechanism by which AGC kinases and MAB4/MEL proteins regulate PIN localization and plant development. acknowledged_ssus: - _id: Bio acknowledgement: We acknowledge Ben Scheres, Christian Luschnig, and Claus Schwechheimer for sharing published material. We thank Monika Hrtyan and Dorota Jaworska at IST Austria and Gerda Lamers and Ward de Winter at IBL Netherlands for technical assistance; Corinna Hartinger, Jakub Hajný, Lesia Rodriguez, Mingyue Li, and Lindy Abas for experimental support; and the Bioimaging Facility at IST Austria and the Bioimaging Core at VIB for imaging support. We are grateful to Christian Luschnig, Lindy Abas, and Roman Pleskot for valuable discussions. We also acknowledge the EMBO for supporting M.G. with a long-term fellowship ( ALTF 1005-2019 ) during the finalization and revision of this manuscript in the laboratory of B.D.R., and we thank R. Pierik for allowing K.V.G. to work on this manuscript during a postdoc in his laboratory at Utrecht University. This work was supported by grants from the European Research Council under the European Union’s Seventh Framework Programme (ERC grant agreements 742985 to J.F., 714055 to B.D.R., and 803048 to M.F.), the Austrian Science Fund (FWF; I 3630-B25 to J.F.), Chemical Sciences (partly) financed by the Dutch Research Council (NWO-CW TOP 700.58.301 to R.O.), the Dutch Research Council (NWO-VICI 865.17.002 to R. Pierik), Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology, Japan (KAKENHI grant 17K17595 to S.N.), the Ministry of Education, Youth and Sports of the Czech Republic (MŠMT project NPUI-LO1417 ), and a China Scholarship Council (to X.W.). article_processing_charge: No article_type: original author: - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: K full_name: Van Gelderen, K last_name: Van Gelderen - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: S full_name: Naramoto, S last_name: Naramoto - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: David full_name: Domjan, David id: C684CD7A-257E-11EA-9B6F-D8588B4F947F last_name: Domjan orcid: 0000-0003-2267-106X - first_name: L full_name: Vcelarova, L last_name: Vcelarova - first_name: Robert full_name: Hauschild, Robert id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87 last_name: Hauschild orcid: 0000-0001-9843-3522 - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: E full_name: de Koning, E last_name: de Koning - first_name: M full_name: van Dop, M last_name: van Dop - first_name: E full_name: Rademacher, E last_name: Rademacher - first_name: S full_name: Janson, S last_name: Janson - first_name: X full_name: Wei, X last_name: Wei - first_name: Gergely full_name: Molnar, Gergely id: 34F1AF46-F248-11E8-B48F-1D18A9856A87 last_name: Molnar - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: B full_name: De Rybel, B last_name: De Rybel - first_name: R full_name: Offringa, R last_name: Offringa - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Glanc M, Van Gelderen K, Hörmayer L, et al. AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells. Current Biology. 2021;31(9):1918-1930. doi:10.1016/j.cub.2021.02.028 apa: Glanc, M., Van Gelderen, K., Hörmayer, L., Tan, S., Naramoto, S., Zhang, X., … Friml, J. (2021). AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells. Current Biology. Elsevier. https://doi.org/10.1016/j.cub.2021.02.028 chicago: Glanc, Matous, K Van Gelderen, Lukas Hörmayer, Shutang Tan, S Naramoto, Xixi Zhang, David Domjan, et al. “AGC Kinases and MAB4/MEL Proteins Maintain PIN Polarity by Limiting Lateral Diffusion in Plant Cells.” Current Biology. Elsevier, 2021. https://doi.org/10.1016/j.cub.2021.02.028. ieee: M. Glanc et al., “AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells,” Current Biology, vol. 31, no. 9. Elsevier, pp. 1918–1930, 2021. ista: Glanc M, Van Gelderen K, Hörmayer L, Tan S, Naramoto S, Zhang X, Domjan D, Vcelarova L, Hauschild R, Johnson AJ, de Koning E, van Dop M, Rademacher E, Janson S, Wei X, Molnar G, Fendrych M, De Rybel B, Offringa R, Friml J. 2021. AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells. Current Biology. 31(9), 1918–1930. mla: Glanc, Matous, et al. “AGC Kinases and MAB4/MEL Proteins Maintain PIN Polarity by Limiting Lateral Diffusion in Plant Cells.” Current Biology, vol. 31, no. 9, Elsevier, 2021, pp. 1918–30, doi:10.1016/j.cub.2021.02.028. short: M. Glanc, K. Van Gelderen, L. Hörmayer, S. Tan, S. Naramoto, X. Zhang, D. Domjan, L. Vcelarova, R. Hauschild, A.J. Johnson, E. de Koning, M. van Dop, E. Rademacher, S. Janson, X. Wei, G. Molnar, M. Fendrych, B. De Rybel, R. Offringa, J. Friml, Current Biology 31 (2021) 1918–1930. date_created: 2021-03-26T12:09:33Z date_published: 2021-03-10T00:00:00Z date_updated: 2023-09-05T13:03:34Z day: '10' ddc: - '580' department: - _id: JiFr doi: 10.1016/j.cub.2021.02.028 ec_funded: 1 external_id: isi: - '000653077800004' pmid: - '33705718' file: - access_level: open_access checksum: b1723040ecfd8c81194185472eb62546 content_type: application/pdf creator: dernst date_created: 2021-04-01T10:53:42Z date_updated: 2021-04-01T10:53:42Z file_id: '9303' file_name: 2021_CurrentBiology_Glanc.pdf file_size: 4324371 relation: main_file success: 1 file_date_updated: 2021-04-01T10:53:42Z has_accepted_license: '1' intvolume: ' 31' isi: 1 issue: '9' language: - iso: eng month: '03' oa: 1 oa_version: Published Version page: 1918-1930 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Current Biology publication_identifier: eissn: - 1879-0445 issn: - 0960-9822 publication_status: published publisher: Elsevier quality_controlled: '1' status: public title: AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 31 year: '2021' ... --- _id: '8824' abstract: - lang: eng text: Plants are able to orient their growth according to gravity, which ultimately controls both shoot and root architecture.1 Gravitropism is a dynamic process whereby gravistimulation induces the asymmetric distribution of the plant hormone auxin, leading to asymmetric growth, organ bending, and subsequent reset of auxin distribution back to the original pre-gravistimulation situation.1, 2, 3 Differential auxin accumulation during the gravitropic response depends on the activity of polarly localized PIN-FORMED (PIN) auxin-efflux carriers.1, 2, 3, 4 In particular, the timing of this dynamic response is regulated by PIN2,5,6 but the underlying molecular mechanisms are poorly understood. Here, we show that MEMBRANE ASSOCIATED KINASE REGULATOR2 (MAKR2) controls the pace of the root gravitropic response. We found that MAKR2 is required for the PIN2 asymmetry during gravitropism by acting as a negative regulator of the cell-surface signaling mediated by the receptor-like kinase TRANSMEMBRANE KINASE1 (TMK1).2,7, 8, 9, 10 Furthermore, we show that the MAKR2 inhibitory effect on TMK1 signaling is antagonized by auxin itself, which triggers rapid MAKR2 membrane dissociation in a TMK1-dependent manner. Our findings suggest that the timing of the root gravitropic response is orchestrated by the reversible inhibition of the TMK1 signaling pathway at the cell surface. acknowledgement: "We thank the SiCE group for discussions and comments; S. Yalovsky, B. Scheres, and the NASC/ABRC collection for providing transgenic Arabidopsis lines and plasmids; L. Kalmbach and M. Barberon for the gift of pLOK180_pFR7m34GW; A. Lacroix, J. Berger, and P. Bolland for plant care; and M. Fendrych for help with microfluidics in the J.F. lab. We acknowledge\r\nthe contribution of the SFR Biosciences (UMS3444/CNRS, US8/Inser m, ENS de Lyon, UCBL) facilities: C. Lionet, E. Chatre, and J. Brocard at LBIPLATIM-MICROSCOPY for assistance with imaging, and V. GuegenChaignon and A. Page at the Protein Science Facility (PSF) for assistance with protein purification and mass spectrometry. Y.J. was funded by ERC\r\ngrant 3363360-APPL under FP/2007–2013. Y.J. and Z.L.N. were funded by an ANR- and NSF-supported ERA-CAPS project (SICOPID: ANR-17-CAPS0003-01/NSF PGRP IOS-1841917). A.I.C.-D. is funded by an ERC consolidator grant (ERC-2015-CoG–683163) and BIO2016-78955 grant from the Spanish Ministry of Economy and Competitiveness. Exchanges between the Y.J. and T.B. laboratories were funded by Tournesol grant 35656NB. B.K.M. was\r\nfunded by the Omics@vib Marie Curie COFUND and Research Foundation Flanders for a postdoctoral fellowship." article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: MM full_name: Marquès-Bueno, MM last_name: Marquès-Bueno - first_name: L full_name: Armengot, L last_name: Armengot - first_name: LC full_name: Noack, LC last_name: Noack - first_name: J full_name: Bareille, J last_name: Bareille - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: MP full_name: Platre, MP last_name: Platre - first_name: V full_name: Bayle, V last_name: Bayle - first_name: M full_name: Liu, M last_name: Liu - first_name: D full_name: Opdenacker, D last_name: Opdenacker - first_name: S full_name: Vanneste, S last_name: Vanneste - first_name: BK full_name: Möller, BK last_name: Möller - first_name: ZL full_name: Nimchuk, ZL last_name: Nimchuk - first_name: T full_name: Beeckman, T last_name: Beeckman - first_name: AI full_name: Caño-Delgado, AI last_name: Caño-Delgado - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Y full_name: Jaillais, Y last_name: Jaillais citation: ama: Marquès-Bueno M, Armengot L, Noack L, et al. Auxin-regulated reversible inhibition of TMK1 signaling by MAKR2 modulates the dynamics of root gravitropism. Current Biology. 2021;31(1). doi:10.1016/j.cub.2020.10.011 apa: Marquès-Bueno, M., Armengot, L., Noack, L., Bareille, J., Rodriguez Solovey, L., Platre, M., … Jaillais, Y. (2021). Auxin-regulated reversible inhibition of TMK1 signaling by MAKR2 modulates the dynamics of root gravitropism. Current Biology. Elsevier. https://doi.org/10.1016/j.cub.2020.10.011 chicago: Marquès-Bueno, MM, L Armengot, LC Noack, J Bareille, Lesia Rodriguez Solovey, MP Platre, V Bayle, et al. “Auxin-Regulated Reversible Inhibition of TMK1 Signaling by MAKR2 Modulates the Dynamics of Root Gravitropism.” Current Biology. Elsevier, 2021. https://doi.org/10.1016/j.cub.2020.10.011. ieee: M. Marquès-Bueno et al., “Auxin-regulated reversible inhibition of TMK1 signaling by MAKR2 modulates the dynamics of root gravitropism,” Current Biology, vol. 31, no. 1. Elsevier, 2021. ista: Marquès-Bueno M, Armengot L, Noack L, Bareille J, Rodriguez Solovey L, Platre M, Bayle V, Liu M, Opdenacker D, Vanneste S, Möller B, Nimchuk Z, Beeckman T, Caño-Delgado A, Friml J, Jaillais Y. 2021. Auxin-regulated reversible inhibition of TMK1 signaling by MAKR2 modulates the dynamics of root gravitropism. Current Biology. 31(1). mla: Marquès-Bueno, MM, et al. “Auxin-Regulated Reversible Inhibition of TMK1 Signaling by MAKR2 Modulates the Dynamics of Root Gravitropism.” Current Biology, vol. 31, no. 1, Elsevier, 2021, doi:10.1016/j.cub.2020.10.011. short: M. Marquès-Bueno, L. Armengot, L. Noack, J. Bareille, L. Rodriguez Solovey, M. Platre, V. Bayle, M. Liu, D. Opdenacker, S. Vanneste, B. Möller, Z. Nimchuk, T. Beeckman, A. Caño-Delgado, J. Friml, Y. Jaillais, Current Biology 31 (2021). date_created: 2020-12-01T13:39:46Z date_published: 2021-01-11T00:00:00Z date_updated: 2023-09-05T13:03:15Z day: '11' ddc: - '570' department: - _id: JiFr doi: 10.1016/j.cub.2020.10.011 external_id: isi: - '000614361000039' pmid: - '33157019' file: - access_level: open_access checksum: 30b3393d841fb2b1e2b22fb42b5c8fff content_type: application/pdf creator: dernst date_created: 2021-02-04T11:37:50Z date_updated: 2021-02-04T11:37:50Z file_id: '9090' file_name: 2021_CurrentBiology_MarquesBueno.pdf file_size: 3458646 relation: main_file success: 1 file_date_updated: 2021-02-04T11:37:50Z has_accepted_license: '1' intvolume: ' 31' isi: 1 issue: '1' language: - iso: eng month: '01' oa: 1 oa_version: Published Version pmid: 1 publication: Current Biology publication_identifier: eissn: - 1879-0445 issn: - 0960-9822 publication_status: published publisher: Elsevier quality_controlled: '1' status: public title: Auxin-regulated reversible inhibition of TMK1 signaling by MAKR2 modulates the dynamics of root gravitropism tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 31 year: '2021' ... --- _id: '9288' abstract: - lang: eng text: "• The phenylpropanoid pathway serves a central role in plant metabolism, providing numerous compounds involved in diverse physiological processes. Most carbon entering the pathway is incorporated into lignin. Although several phenylpropanoid pathway mutants show seedling growth arrest, the role for lignin in seedling growth and development is unexplored.\r\n• We use complementary pharmacological and genetic approaches to block CINNAMATE‐4‐HYDROXYLASE (C4H) functionality in Arabidopsis seedlings and a set of molecular and biochemical techniques to investigate the underlying phenotypes.\r\n• Blocking C4H resulted in reduced lateral rooting and increased adventitious rooting apically in the hypocotyl. These phenotypes coincided with an inhibition in auxin transport. The upstream accumulation in cis‐cinnamic acid was found to likely cause polar auxin transport inhibition. Conversely, a downstream depletion in lignin perturbed phloem‐mediated auxin transport. Restoring lignin deposition effectively reestablished phloem transport and, accordingly, auxin homeostasis.\r\n• Our results show that the accumulation of bioactive intermediates and depletion in lignin jointly cause the aberrant phenotypes upon blocking C4H, and demonstrate that proper deposition of lignin is essential for the establishment of auxin distribution in seedlings. Our data position the phenylpropanoid pathway and lignin in a new physiological framework, consolidating their importance in plant growth and development." article_processing_charge: No article_type: original author: - first_name: I full_name: El Houari, I last_name: El Houari - first_name: C full_name: Van Beirs, C last_name: Van Beirs - first_name: HE full_name: Arents, HE last_name: Arents - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: A full_name: Chanoca, A last_name: Chanoca - first_name: D full_name: Opdenacker, D last_name: Opdenacker - first_name: J full_name: Pollier, J last_name: Pollier - first_name: V full_name: Storme, V last_name: Storme - first_name: W full_name: Steenackers, W last_name: Steenackers - first_name: M full_name: Quareshy, M last_name: Quareshy - first_name: R full_name: Napier, R last_name: Napier - first_name: T full_name: Beeckman, T last_name: Beeckman - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: B full_name: De Rybel, B last_name: De Rybel - first_name: W full_name: Boerjan, W last_name: Boerjan - first_name: B full_name: Vanholme, B last_name: Vanholme citation: ama: El Houari I, Van Beirs C, Arents H, et al. Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport. New Phytologist. 2021;230(6):2275-2291. doi:10.1111/nph.17349 apa: El Houari, I., Van Beirs, C., Arents, H., Han, H., Chanoca, A., Opdenacker, D., … Vanholme, B. (2021). Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport. New Phytologist. Wiley. https://doi.org/10.1111/nph.17349 chicago: El Houari, I, C Van Beirs, HE Arents, Huibin Han, A Chanoca, D Opdenacker, J Pollier, et al. “Seedling Developmental Defects upon Blocking CINNAMATE-4-HYDROXYLASE Are Caused by Perturbations in Auxin Transport.” New Phytologist. Wiley, 2021. https://doi.org/10.1111/nph.17349. ieee: I. El Houari et al., “Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport,” New Phytologist, vol. 230, no. 6. Wiley, pp. 2275–2291, 2021. ista: El Houari I, Van Beirs C, Arents H, Han H, Chanoca A, Opdenacker D, Pollier J, Storme V, Steenackers W, Quareshy M, Napier R, Beeckman T, Friml J, De Rybel B, Boerjan W, Vanholme B. 2021. Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport. New Phytologist. 230(6), 2275–2291. mla: El Houari, I., et al. “Seedling Developmental Defects upon Blocking CINNAMATE-4-HYDROXYLASE Are Caused by Perturbations in Auxin Transport.” New Phytologist, vol. 230, no. 6, Wiley, 2021, pp. 2275–91, doi:10.1111/nph.17349. short: I. El Houari, C. Van Beirs, H. Arents, H. Han, A. Chanoca, D. Opdenacker, J. Pollier, V. Storme, W. Steenackers, M. Quareshy, R. Napier, T. Beeckman, J. Friml, B. De Rybel, W. Boerjan, B. Vanholme, New Phytologist 230 (2021) 2275–2291. date_created: 2021-03-26T12:09:01Z date_published: 2021-03-17T00:00:00Z date_updated: 2023-09-05T15:46:55Z day: '17' department: - _id: JiFr doi: 10.1111/nph.17349 external_id: isi: - '000639552400001' pmid: - '33728703' intvolume: ' 230' isi: 1 issue: '6' language: - iso: eng main_file_link: - open_access: '1' url: https://biblio.ugent.be/publication/8703799/file/8703800.pdf month: '03' oa: 1 oa_version: Published Version page: 2275-2291 pmid: 1 publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646x publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 230 year: '2021' ... --- _id: '8608' abstract: - lang: eng text: To adapt to the diverse array of biotic and abiotic cues, plants have evolved sophisticated mechanisms to sense changes in environmental conditions and modulate their growth. Growth-promoting hormones and defence signalling fine tune plant development antagonistically. During host-pathogen interactions, this defence-growth trade-off is mediated by the counteractive effects of the defence hormone salicylic acid (SA) and the growth hormone auxin. Here we revealed an underlying mechanism of SA regulating auxin signalling by constraining the plasma membrane dynamics of PIN2 auxin efflux transporter in Arabidopsis thaliana roots. The lateral diffusion of PIN2 proteins is constrained by SA signalling, during which PIN2 proteins are condensed into hyperclusters depending on REM1.2-mediated nanodomain compartmentalisation. Furthermore, membrane nanodomain compartmentalisation by SA or Remorin (REM) assembly significantly suppressed clathrin-mediated endocytosis. Consequently, SA-induced heterogeneous surface condensation disrupted asymmetric auxin distribution and the resultant gravitropic response. Our results demonstrated a defence-growth trade-off mechanism by which SA signalling crosstalked with auxin transport by concentrating membrane-resident PIN2 into heterogeneous compartments. acknowledgement: This work was supported by the National Key Research andDevelopment Programme of China (2017YFA0506100), theNational Natural Science Foundation of China (31870170 and31701168), and the Fok Ying Tung Education Foundation(161027) to XC; NTU startup grant (M4081533) and NIM/01/2016 (NTU, Singapore) to YM. We thank Lei Shi andZhongquan Lin for microscopy assistance. article_processing_charge: No article_type: original author: - first_name: M full_name: Ke, M last_name: Ke - first_name: Z full_name: Ma, Z last_name: Ma - first_name: D full_name: Wang, D last_name: Wang - first_name: Y full_name: Sun, Y last_name: Sun - first_name: C full_name: Wen, C last_name: Wen - first_name: D full_name: Huang, D last_name: Huang - first_name: Z full_name: Chen, Z last_name: Chen - first_name: L full_name: Yang, L last_name: Yang - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: R full_name: Li, R last_name: Li - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Y full_name: Miao, Y last_name: Miao - first_name: X full_name: Chen, X last_name: Chen citation: ama: Ke M, Ma Z, Wang D, et al. Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana. New Phytologist. 2021;229(2):963-978. doi:10.1111/nph.16915 apa: Ke, M., Ma, Z., Wang, D., Sun, Y., Wen, C., Huang, D., … Chen, X. (2021). Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana. New Phytologist. Wiley. https://doi.org/10.1111/nph.16915 chicago: Ke, M, Z Ma, D Wang, Y Sun, C Wen, D Huang, Z Chen, et al. “Salicylic Acid Regulates PIN2 Auxin Transporter Hyper-Clustering and Root Gravitropic Growth via Remorin-Dependent Lipid Nanodomain Organization in Arabidopsis Thaliana.” New Phytologist. Wiley, 2021. https://doi.org/10.1111/nph.16915. ieee: M. Ke et al., “Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana,” New Phytologist, vol. 229, no. 2. Wiley, pp. 963–978, 2021. ista: Ke M, Ma Z, Wang D, Sun Y, Wen C, Huang D, Chen Z, Yang L, Tan S, Li R, Friml J, Miao Y, Chen X. 2021. Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana. New Phytologist. 229(2), 963–978. mla: Ke, M., et al. “Salicylic Acid Regulates PIN2 Auxin Transporter Hyper-Clustering and Root Gravitropic Growth via Remorin-Dependent Lipid Nanodomain Organization in Arabidopsis Thaliana.” New Phytologist, vol. 229, no. 2, Wiley, 2021, pp. 963–78, doi:10.1111/nph.16915. short: M. Ke, Z. Ma, D. Wang, Y. Sun, C. Wen, D. Huang, Z. Chen, L. Yang, S. Tan, R. Li, J. Friml, Y. Miao, X. Chen, New Phytologist 229 (2021) 963–978. date_created: 2020-10-05T12:45:36Z date_published: 2021-01-01T00:00:00Z date_updated: 2023-09-05T16:06:24Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/nph.16915 external_id: isi: - '000573568000001' pmid: - '32901934' file: - access_level: open_access checksum: d36b6a8c6fafab66264e0d27114dae63 content_type: application/pdf creator: dernst date_created: 2021-02-04T09:53:16Z date_updated: 2021-02-04T09:53:16Z file_id: '9085' file_name: 2021_NewPhytologist_Ke.pdf file_size: 3674502 relation: main_file success: 1 file_date_updated: 2021-02-04T09:53:16Z has_accepted_license: '1' intvolume: ' 229' isi: 1 issue: '2' language: - iso: eng month: '01' oa: 1 oa_version: Published Version page: 963-978 pmid: 1 publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646x publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 229 year: '2021' ... --- _id: '9298' abstract: - lang: eng text: 'In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field. ' acknowledgement: This work was supported by the National Institute of General Medical Sciences [GM131919]. Due to space and other limitations, it is not possible to include all other sources of financial support. article_processing_charge: No article_type: review author: - first_name: Daniel J. full_name: Klionsky, Daniel J. last_name: Klionsky - first_name: Amal Kamal full_name: Abdel-Aziz, Amal Kamal last_name: Abdel-Aziz - first_name: Sara full_name: Abdelfatah, Sara last_name: Abdelfatah - first_name: Mahmoud full_name: Abdellatif, Mahmoud last_name: Abdellatif - first_name: Asghar full_name: Abdoli, Asghar last_name: Abdoli - first_name: Steffen full_name: Abel, Steffen last_name: Abel - first_name: Hagai full_name: Abeliovich, Hagai last_name: Abeliovich - first_name: Marie H. full_name: Abildgaard, Marie H. last_name: Abildgaard - first_name: Yakubu Princely full_name: Abudu, Yakubu Princely last_name: Abudu - first_name: Abraham full_name: Acevedo-Arozena, Abraham last_name: Acevedo-Arozena - first_name: Iannis E. full_name: Adamopoulos, Iannis E. last_name: Adamopoulos - first_name: Khosrow full_name: Adeli, Khosrow last_name: Adeli - first_name: Timon E. full_name: Adolph, Timon E. last_name: Adolph - first_name: Annagrazia full_name: Adornetto, Annagrazia last_name: Adornetto - first_name: Elma full_name: Aflaki, Elma last_name: Aflaki - first_name: Galila full_name: Agam, Galila last_name: Agam - first_name: Anupam full_name: Agarwal, Anupam last_name: Agarwal - first_name: Bharat B. full_name: Aggarwal, Bharat B. last_name: Aggarwal - first_name: Maria full_name: Agnello, Maria last_name: Agnello - first_name: Patrizia full_name: Agostinis, Patrizia last_name: Agostinis - first_name: Javed N. full_name: Agrewala, Javed N. last_name: Agrewala - first_name: Alexander full_name: Agrotis, Alexander last_name: Agrotis - first_name: Patricia V. full_name: Aguilar, Patricia V. last_name: Aguilar - first_name: S. Tariq full_name: Ahmad, S. Tariq last_name: Ahmad - first_name: Zubair M. full_name: Ahmed, Zubair M. last_name: Ahmed - first_name: Ulises full_name: Ahumada-Castro, Ulises last_name: Ahumada-Castro - first_name: Sonja full_name: Aits, Sonja last_name: Aits - first_name: Shu full_name: Aizawa, Shu last_name: Aizawa - first_name: Yunus full_name: Akkoc, Yunus last_name: Akkoc - first_name: Tonia full_name: Akoumianaki, Tonia last_name: Akoumianaki - first_name: Hafize Aysin full_name: Akpinar, Hafize Aysin last_name: Akpinar - first_name: Ahmed M. full_name: Al-Abd, Ahmed M. last_name: Al-Abd - first_name: Lina full_name: Al-Akra, Lina last_name: Al-Akra - first_name: Abeer full_name: Al-Gharaibeh, Abeer last_name: Al-Gharaibeh - first_name: Moulay A. full_name: Alaoui-Jamali, Moulay A. last_name: Alaoui-Jamali - first_name: Simon full_name: Alberti, Simon last_name: Alberti - first_name: Elísabet full_name: Alcocer-Gómez, Elísabet last_name: Alcocer-Gómez - first_name: Cristiano full_name: Alessandri, Cristiano last_name: Alessandri - first_name: Muhammad full_name: Ali, Muhammad last_name: Ali - first_name: M. Abdul full_name: Alim Al-Bari, M. Abdul last_name: Alim Al-Bari - first_name: Saeb full_name: Aliwaini, Saeb last_name: Aliwaini - first_name: Javad full_name: Alizadeh, Javad last_name: Alizadeh - first_name: Eugènia full_name: Almacellas, Eugènia last_name: Almacellas - first_name: Alexandru full_name: Almasan, Alexandru last_name: Almasan - first_name: Alicia full_name: Alonso, Alicia last_name: Alonso - first_name: Guillermo D. full_name: Alonso, Guillermo D. last_name: Alonso - first_name: Nihal full_name: Altan-Bonnet, Nihal last_name: Altan-Bonnet - first_name: Dario C. full_name: Altieri, Dario C. last_name: Altieri - first_name: Élida M.C. full_name: Álvarez, Élida M.C. last_name: Álvarez - first_name: Sara full_name: Alves, Sara last_name: Alves - first_name: Cristine full_name: Alves Da Costa, Cristine last_name: Alves Da Costa - first_name: Mazen M. full_name: Alzaharna, Mazen M. last_name: Alzaharna - first_name: Marialaura full_name: Amadio, Marialaura last_name: Amadio - first_name: Consuelo full_name: Amantini, Consuelo last_name: Amantini - first_name: Cristina full_name: Amaral, Cristina last_name: Amaral - first_name: Susanna full_name: Ambrosio, Susanna last_name: Ambrosio - first_name: Amal O. full_name: Amer, Amal O. last_name: Amer - first_name: Veena full_name: Ammanathan, Veena last_name: Ammanathan - first_name: Zhenyi full_name: An, Zhenyi last_name: An - first_name: Stig U. full_name: Andersen, Stig U. last_name: Andersen - first_name: Shaida A. full_name: Andrabi, Shaida A. last_name: Andrabi - first_name: Magaiver full_name: Andrade-Silva, Magaiver last_name: Andrade-Silva - first_name: Allen M. full_name: Andres, Allen M. last_name: Andres - first_name: Sabrina full_name: Angelini, Sabrina last_name: Angelini - first_name: David full_name: Ann, David last_name: Ann - first_name: Uche C. full_name: Anozie, Uche C. last_name: Anozie - first_name: Mohammad Y. full_name: Ansari, Mohammad Y. last_name: Ansari - first_name: Pedro full_name: Antas, Pedro last_name: Antas - first_name: Adam full_name: Antebi, Adam last_name: Antebi - first_name: Zuriñe full_name: Antón, Zuriñe last_name: Antón - first_name: Tahira full_name: Anwar, Tahira last_name: Anwar - first_name: Lionel full_name: Apetoh, Lionel last_name: Apetoh - first_name: Nadezda full_name: Apostolova, Nadezda last_name: Apostolova - first_name: Toshiyuki full_name: Araki, Toshiyuki last_name: Araki - first_name: Yasuhiro full_name: Araki, Yasuhiro last_name: Araki - first_name: Kohei full_name: Arasaki, Kohei last_name: Arasaki - first_name: Wagner L. full_name: Araújo, Wagner L. last_name: Araújo - first_name: Jun full_name: Araya, Jun last_name: Araya - first_name: Catherine full_name: Arden, Catherine last_name: Arden - first_name: Maria Angeles full_name: Arévalo, Maria Angeles last_name: Arévalo - first_name: Sandro full_name: Arguelles, Sandro last_name: Arguelles - first_name: Esperanza full_name: Arias, Esperanza last_name: Arias - first_name: Jyothi full_name: Arikkath, Jyothi last_name: Arikkath - first_name: Hirokazu full_name: Arimoto, Hirokazu last_name: Arimoto - first_name: Aileen R. full_name: Ariosa, Aileen R. last_name: Ariosa - first_name: Darius full_name: Armstrong-James, Darius last_name: Armstrong-James - first_name: Laetitia full_name: Arnauné-Pelloquin, Laetitia last_name: Arnauné-Pelloquin - first_name: Angeles full_name: Aroca, Angeles last_name: Aroca - first_name: Daniela S. full_name: Arroyo, Daniela S. last_name: Arroyo - first_name: Ivica full_name: Arsov, Ivica last_name: Arsov - first_name: Rubén full_name: Artero, Rubén last_name: Artero - first_name: Dalia Maria Lucia full_name: Asaro, Dalia Maria Lucia last_name: Asaro - first_name: Michael full_name: Aschner, Michael last_name: Aschner - first_name: Milad full_name: Ashrafizadeh, Milad last_name: Ashrafizadeh - first_name: Osnat full_name: Ashur-Fabian, Osnat last_name: Ashur-Fabian - first_name: Atanas G. full_name: Atanasov, Atanas G. last_name: Atanasov - first_name: Alicia K. full_name: Au, Alicia K. last_name: Au - first_name: Patrick full_name: Auberger, Patrick last_name: Auberger - first_name: Holger W. full_name: Auner, Holger W. last_name: Auner - first_name: Laure full_name: Aurelian, Laure last_name: Aurelian - first_name: Riccardo full_name: Autelli, Riccardo last_name: Autelli - first_name: Laura full_name: Avagliano, Laura last_name: Avagliano - first_name: Yenniffer full_name: Ávalos, Yenniffer last_name: Ávalos - first_name: Sanja full_name: Aveic, Sanja last_name: Aveic - first_name: Célia Alexandra full_name: Aveleira, Célia Alexandra last_name: Aveleira - first_name: Tamar full_name: Avin-Wittenberg, Tamar last_name: Avin-Wittenberg - first_name: Yucel full_name: Aydin, Yucel last_name: Aydin - first_name: Scott full_name: Ayton, Scott last_name: Ayton - first_name: Srinivas full_name: Ayyadevara, Srinivas last_name: Ayyadevara - first_name: Maria full_name: Azzopardi, Maria last_name: Azzopardi - first_name: Misuzu full_name: Baba, Misuzu last_name: Baba - first_name: Jonathan M. full_name: Backer, Jonathan M. last_name: Backer - first_name: Steven K. full_name: Backues, Steven K. last_name: Backues - first_name: Dong Hun full_name: Bae, Dong Hun last_name: Bae - first_name: Ok Nam full_name: Bae, Ok Nam last_name: Bae - first_name: Soo Han full_name: Bae, Soo Han last_name: Bae - first_name: Eric H. full_name: Baehrecke, Eric H. last_name: Baehrecke - first_name: Ahruem full_name: Baek, Ahruem last_name: Baek - first_name: Seung Hoon full_name: Baek, Seung Hoon last_name: Baek - first_name: Sung Hee full_name: Baek, Sung Hee last_name: Baek - first_name: Giacinto full_name: Bagetta, Giacinto last_name: Bagetta - first_name: Agnieszka full_name: Bagniewska-Zadworna, Agnieszka last_name: Bagniewska-Zadworna - first_name: Hua full_name: Bai, Hua last_name: Bai - first_name: Jie full_name: Bai, Jie last_name: Bai - first_name: Xiyuan full_name: Bai, Xiyuan last_name: Bai - first_name: Yidong full_name: Bai, Yidong last_name: Bai - first_name: Nandadulal full_name: Bairagi, Nandadulal last_name: Bairagi - first_name: Shounak full_name: Baksi, Shounak last_name: Baksi - first_name: Teresa full_name: Balbi, Teresa last_name: Balbi - first_name: Cosima T. full_name: Baldari, Cosima T. last_name: Baldari - first_name: Walter full_name: Balduini, Walter last_name: Balduini - first_name: Andrea full_name: Ballabio, Andrea last_name: Ballabio - first_name: Maria full_name: Ballester, Maria last_name: Ballester - first_name: Salma full_name: Balazadeh, Salma last_name: Balazadeh - first_name: Rena full_name: Balzan, Rena last_name: Balzan - first_name: Rina full_name: Bandopadhyay, Rina last_name: Bandopadhyay - first_name: Sreeparna full_name: Banerjee, Sreeparna last_name: Banerjee - first_name: Sulagna full_name: Banerjee, Sulagna last_name: Banerjee - first_name: Ágnes full_name: Bánréti, Ágnes last_name: Bánréti - first_name: Yan full_name: Bao, Yan last_name: Bao - first_name: Mauricio S. full_name: Baptista, Mauricio S. last_name: Baptista - first_name: Alessandra full_name: Baracca, Alessandra last_name: Baracca - first_name: Cristiana full_name: Barbati, Cristiana last_name: Barbati - first_name: Ariadna full_name: Bargiela, Ariadna last_name: Bargiela - first_name: Daniela full_name: Barilà, Daniela last_name: Barilà - first_name: Peter G. full_name: Barlow, Peter G. last_name: Barlow - first_name: Sami J. full_name: Barmada, Sami J. last_name: Barmada - first_name: Esther full_name: Barreiro, Esther last_name: Barreiro - first_name: George E. full_name: Barreto, George E. last_name: Barreto - first_name: Jiri full_name: Bartek, Jiri last_name: Bartek - first_name: Bonnie full_name: Bartel, Bonnie last_name: Bartel - first_name: Alberto full_name: Bartolome, Alberto last_name: Bartolome - first_name: Gaurav R. full_name: Barve, Gaurav R. last_name: Barve - first_name: Suresh H. full_name: Basagoudanavar, Suresh H. last_name: Basagoudanavar - first_name: Diane C. full_name: Bassham, Diane C. last_name: Bassham - first_name: Robert C. full_name: Bast, Robert C. last_name: Bast - first_name: Alakananda full_name: Basu, Alakananda last_name: Basu - first_name: Henri full_name: Batoko, Henri last_name: Batoko - first_name: Isabella full_name: Batten, Isabella last_name: Batten - first_name: Etienne E. full_name: Baulieu, Etienne E. last_name: Baulieu - first_name: Bradley L. full_name: Baumgarner, Bradley L. last_name: Baumgarner - first_name: Jagadeesh full_name: Bayry, Jagadeesh last_name: Bayry - first_name: Rupert full_name: Beale, Rupert last_name: Beale - first_name: Isabelle full_name: Beau, Isabelle last_name: Beau - first_name: Florian full_name: Beaumatin, Florian last_name: Beaumatin - first_name: Luiz R.G. full_name: Bechara, Luiz R.G. last_name: Bechara - first_name: George R. full_name: Beck, George R. last_name: Beck - first_name: Michael F. full_name: Beers, Michael F. last_name: Beers - first_name: Jakob full_name: Begun, Jakob last_name: Begun - first_name: Christian full_name: Behrends, Christian last_name: Behrends - first_name: Georg M.N. full_name: Behrens, Georg M.N. last_name: Behrens - first_name: Roberto full_name: Bei, Roberto last_name: Bei - first_name: Eloy full_name: Bejarano, Eloy last_name: Bejarano - first_name: Shai full_name: Bel, Shai last_name: Bel - first_name: Christian full_name: Behl, Christian last_name: Behl - first_name: Amine full_name: Belaid, Amine last_name: Belaid - first_name: Naïma full_name: Belgareh-Touzé, Naïma last_name: Belgareh-Touzé - first_name: Cristina full_name: Bellarosa, Cristina last_name: Bellarosa - first_name: Francesca full_name: Belleudi, Francesca last_name: Belleudi - first_name: Melissa full_name: Belló Pérez, Melissa last_name: Belló Pérez - first_name: Raquel full_name: Bello-Morales, Raquel last_name: Bello-Morales - first_name: Jackeline Soares De Oliveira full_name: Beltran, Jackeline Soares De Oliveira last_name: Beltran - first_name: Sebastián full_name: Beltran, Sebastián last_name: Beltran - first_name: Doris Mangiaracina full_name: Benbrook, Doris Mangiaracina last_name: Benbrook - first_name: Mykolas full_name: Bendorius, Mykolas last_name: Bendorius - first_name: Bruno A. full_name: Benitez, Bruno A. last_name: Benitez - first_name: Irene full_name: Benito-Cuesta, Irene last_name: Benito-Cuesta - first_name: Julien full_name: Bensalem, Julien last_name: Bensalem - first_name: Martin W. full_name: Berchtold, Martin W. last_name: Berchtold - first_name: Sabina full_name: Berezowska, Sabina last_name: Berezowska - first_name: Daniele full_name: Bergamaschi, Daniele last_name: Bergamaschi - first_name: Matteo full_name: Bergami, Matteo last_name: Bergami - first_name: Andreas full_name: Bergmann, Andreas last_name: Bergmann - first_name: Laura full_name: Berliocchi, Laura last_name: Berliocchi - first_name: Clarisse full_name: Berlioz-Torrent, Clarisse last_name: Berlioz-Torrent - first_name: Amélie full_name: Bernard, Amélie last_name: Bernard - first_name: Lionel full_name: Berthoux, Lionel last_name: Berthoux - first_name: Cagri G. full_name: Besirli, Cagri G. last_name: Besirli - first_name: Sebastien full_name: Besteiro, Sebastien last_name: Besteiro - first_name: Virginie M. full_name: Betin, Virginie M. last_name: Betin - first_name: Rudi full_name: Beyaert, Rudi last_name: Beyaert - first_name: Jelena S. full_name: Bezbradica, Jelena S. last_name: Bezbradica - first_name: Kiran full_name: Bhaskar, Kiran last_name: Bhaskar - first_name: Ingrid full_name: Bhatia-Kissova, Ingrid last_name: Bhatia-Kissova - first_name: Resham full_name: Bhattacharya, Resham last_name: Bhattacharya - first_name: Sujoy full_name: Bhattacharya, Sujoy last_name: Bhattacharya - first_name: Shalmoli full_name: Bhattacharyya, Shalmoli last_name: Bhattacharyya - first_name: Md Shenuarin full_name: Bhuiyan, Md Shenuarin last_name: Bhuiyan - first_name: Sujit Kumar full_name: Bhutia, Sujit Kumar last_name: Bhutia - first_name: Lanrong full_name: Bi, Lanrong last_name: Bi - first_name: Xiaolin full_name: Bi, Xiaolin last_name: Bi - first_name: Trevor J. full_name: Biden, Trevor J. last_name: Biden - first_name: Krikor full_name: Bijian, Krikor last_name: Bijian - first_name: Viktor A. full_name: Billes, Viktor A. last_name: Billes - first_name: Nadine full_name: Binart, Nadine last_name: Binart - first_name: Claudia full_name: Bincoletto, Claudia last_name: Bincoletto - first_name: Asa B. full_name: Birgisdottir, Asa B. last_name: Birgisdottir - first_name: Geir full_name: Bjorkoy, Geir last_name: Bjorkoy - first_name: Gonzalo full_name: Blanco, Gonzalo last_name: Blanco - first_name: Ana full_name: Blas-Garcia, Ana last_name: Blas-Garcia - first_name: Janusz full_name: Blasiak, Janusz last_name: Blasiak - first_name: Robert full_name: Blomgran, Robert last_name: Blomgran - first_name: Klas full_name: Blomgren, Klas last_name: Blomgren - first_name: Janice S. full_name: Blum, Janice S. last_name: Blum - first_name: Emilio full_name: Boada-Romero, Emilio last_name: Boada-Romero - first_name: Mirta full_name: Boban, Mirta last_name: Boban - first_name: Kathleen full_name: Boesze-Battaglia, Kathleen last_name: Boesze-Battaglia - first_name: Philippe full_name: Boeuf, Philippe last_name: Boeuf - first_name: Barry full_name: Boland, Barry last_name: Boland - first_name: Pascale full_name: Bomont, Pascale last_name: Bomont - first_name: Paolo full_name: Bonaldo, Paolo last_name: Bonaldo - first_name: Srinivasa Reddy full_name: Bonam, Srinivasa Reddy last_name: Bonam - first_name: Laura full_name: Bonfili, Laura last_name: Bonfili - first_name: Juan S. full_name: Bonifacino, Juan S. last_name: Bonifacino - first_name: Brian A. full_name: Boone, Brian A. last_name: Boone - first_name: Martin D. full_name: Bootman, Martin D. last_name: Bootman - first_name: Matteo full_name: Bordi, Matteo last_name: Bordi - first_name: Christoph full_name: Borner, Christoph last_name: Borner - first_name: Beat C. full_name: Bornhauser, Beat C. last_name: Bornhauser - first_name: Gautam full_name: Borthakur, Gautam last_name: Borthakur - first_name: Jürgen full_name: Bosch, Jürgen last_name: Bosch - first_name: Santanu full_name: Bose, Santanu last_name: Bose - first_name: Luis M. full_name: Botana, Luis M. last_name: Botana - first_name: Juan full_name: Botas, Juan last_name: Botas - first_name: Chantal M. full_name: Boulanger, Chantal M. last_name: Boulanger - first_name: Michael E. full_name: Boulton, Michael E. last_name: Boulton - first_name: Mathieu full_name: Bourdenx, Mathieu last_name: Bourdenx - first_name: Benjamin full_name: Bourgeois, Benjamin last_name: Bourgeois - first_name: Nollaig M. full_name: Bourke, Nollaig M. last_name: Bourke - first_name: Guilhem full_name: Bousquet, Guilhem last_name: Bousquet - first_name: Patricia full_name: Boya, Patricia last_name: Boya - first_name: Peter V. full_name: Bozhkov, Peter V. last_name: Bozhkov - first_name: Luiz H.M. full_name: Bozi, Luiz H.M. last_name: Bozi - first_name: Tolga O. full_name: Bozkurt, Tolga O. last_name: Bozkurt - first_name: Doug E. full_name: Brackney, Doug E. last_name: Brackney - first_name: Christian H. full_name: Brandts, Christian H. last_name: Brandts - first_name: Ralf J. full_name: Braun, Ralf J. last_name: Braun - first_name: Gerhard H. full_name: Braus, Gerhard H. last_name: Braus - first_name: Roberto full_name: Bravo-Sagua, Roberto last_name: Bravo-Sagua - first_name: José M. full_name: Bravo-San Pedro, José M. last_name: Bravo-San Pedro - first_name: Patrick full_name: Brest, Patrick last_name: Brest - first_name: Marie Agnès full_name: Bringer, Marie Agnès last_name: Bringer - first_name: Alfredo full_name: Briones-Herrera, Alfredo last_name: Briones-Herrera - first_name: V. Courtney full_name: Broaddus, V. Courtney last_name: Broaddus - first_name: Peter full_name: Brodersen, Peter last_name: Brodersen - first_name: Jeffrey L. full_name: Brodsky, Jeffrey L. last_name: Brodsky - first_name: Steven L. full_name: Brody, Steven L. last_name: Brody - first_name: Paola G. full_name: Bronson, Paola G. last_name: Bronson - first_name: Jeff M. full_name: Bronstein, Jeff M. last_name: Bronstein - first_name: Carolyn N. full_name: Brown, Carolyn N. last_name: Brown - first_name: Rhoderick E. full_name: Brown, Rhoderick E. last_name: Brown - first_name: Patricia C. full_name: Brum, Patricia C. last_name: Brum - first_name: John H. full_name: Brumell, John H. last_name: Brumell - first_name: Nicola full_name: Brunetti-Pierri, Nicola last_name: Brunetti-Pierri - first_name: Daniele full_name: Bruno, Daniele last_name: Bruno - first_name: Robert J. full_name: Bryson-Richardson, Robert J. last_name: Bryson-Richardson - first_name: Cecilia full_name: Bucci, Cecilia last_name: Bucci - first_name: Carmen full_name: Buchrieser, Carmen last_name: Buchrieser - first_name: Marta full_name: Bueno, Marta last_name: Bueno - first_name: Laura Elisa full_name: Buitrago-Molina, Laura Elisa last_name: Buitrago-Molina - first_name: Simone full_name: Buraschi, Simone last_name: Buraschi - first_name: Shilpa full_name: Buch, Shilpa last_name: Buch - first_name: J. Ross full_name: Buchan, J. Ross last_name: Buchan - first_name: Erin M. full_name: Buckingham, Erin M. last_name: Buckingham - first_name: Hikmet full_name: Budak, Hikmet last_name: Budak - first_name: Mauricio full_name: Budini, Mauricio last_name: Budini - first_name: Geert full_name: Bultynck, Geert last_name: Bultynck - first_name: Florin full_name: Burada, Florin last_name: Burada - first_name: Joseph R. full_name: Burgoyne, Joseph R. last_name: Burgoyne - first_name: M. Isabel full_name: Burón, M. Isabel last_name: Burón - first_name: Victor full_name: Bustos, Victor last_name: Bustos - first_name: Sabrina full_name: Büttner, Sabrina last_name: Büttner - first_name: Elena full_name: Butturini, Elena last_name: Butturini - first_name: Aaron full_name: Byrd, Aaron last_name: Byrd - first_name: Isabel full_name: Cabas, Isabel last_name: Cabas - first_name: Sandra full_name: Cabrera-Benitez, Sandra last_name: Cabrera-Benitez - first_name: Ken full_name: Cadwell, Ken last_name: Cadwell - first_name: Jingjing full_name: Cai, Jingjing last_name: Cai - first_name: Lu full_name: Cai, Lu last_name: Cai - first_name: Qian full_name: Cai, Qian last_name: Cai - first_name: Montserrat full_name: Cairó, Montserrat last_name: Cairó - first_name: Jose A. full_name: Calbet, Jose A. last_name: Calbet - first_name: Guy A. full_name: Caldwell, Guy A. last_name: Caldwell - first_name: Kim A. full_name: Caldwell, Kim A. last_name: Caldwell - first_name: Jarrod A. full_name: Call, Jarrod A. last_name: Call - first_name: Riccardo full_name: Calvani, Riccardo last_name: Calvani - first_name: Ana C. full_name: Calvo, Ana C. last_name: Calvo - first_name: Miguel full_name: Calvo-Rubio Barrera, Miguel last_name: Calvo-Rubio Barrera - first_name: Niels O.S. full_name: Camara, Niels O.S. last_name: Camara - first_name: Jacques H. full_name: Camonis, Jacques H. last_name: Camonis - first_name: Nadine full_name: Camougrand, Nadine last_name: Camougrand - first_name: Michelangelo full_name: Campanella, Michelangelo last_name: Campanella - first_name: Edward M. full_name: Campbell, Edward M. last_name: Campbell - first_name: François Xavier full_name: Campbell-Valois, François Xavier last_name: Campbell-Valois - first_name: Silvia full_name: Campello, Silvia last_name: Campello - first_name: Ilaria full_name: Campesi, Ilaria last_name: Campesi - first_name: Juliane C. full_name: Campos, Juliane C. last_name: Campos - first_name: Olivier full_name: Camuzard, Olivier last_name: Camuzard - first_name: Jorge full_name: Cancino, Jorge last_name: Cancino - first_name: Danilo full_name: Candido De Almeida, Danilo last_name: Candido De Almeida - first_name: Laura full_name: Canesi, Laura last_name: Canesi - first_name: Isabella full_name: Caniggia, Isabella last_name: Caniggia - first_name: Barbara full_name: Canonico, Barbara last_name: Canonico - first_name: Carles full_name: Cantí, Carles last_name: Cantí - first_name: Bin full_name: Cao, Bin last_name: Cao - first_name: Michele full_name: Caraglia, Michele last_name: Caraglia - first_name: Beatriz full_name: Caramés, Beatriz last_name: Caramés - first_name: Evie H. full_name: Carchman, Evie H. last_name: Carchman - first_name: Elena full_name: Cardenal-Muñoz, Elena last_name: Cardenal-Muñoz - first_name: Cesar full_name: Cardenas, Cesar last_name: Cardenas - first_name: Luis full_name: Cardenas, Luis last_name: Cardenas - first_name: Sandra M. full_name: Cardoso, Sandra M. last_name: Cardoso - first_name: Jennifer S. full_name: Carew, Jennifer S. last_name: Carew - first_name: Georges F. full_name: Carle, Georges F. last_name: Carle - first_name: Gillian full_name: Carleton, Gillian last_name: Carleton - first_name: Silvia full_name: Carloni, Silvia last_name: Carloni - first_name: Didac full_name: Carmona-Gutierrez, Didac last_name: Carmona-Gutierrez - first_name: Leticia A. full_name: Carneiro, Leticia A. last_name: Carneiro - first_name: Oliana full_name: Carnevali, Oliana last_name: Carnevali - first_name: Julian M. full_name: Carosi, Julian M. last_name: Carosi - first_name: Serena full_name: Carra, Serena last_name: Carra - first_name: Alice full_name: Carrier, Alice last_name: Carrier - first_name: Lucie full_name: Carrier, Lucie last_name: Carrier - first_name: Bernadette full_name: Carroll, Bernadette last_name: Carroll - first_name: A. 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Brent last_name: Carter - first_name: Andreia Neves full_name: Carvalho, Andreia Neves last_name: Carvalho - first_name: Magali full_name: Casanova, Magali last_name: Casanova - first_name: Caty full_name: Casas, Caty last_name: Casas - first_name: Josefina full_name: Casas, Josefina last_name: Casas - first_name: Chiara full_name: Cassioli, Chiara last_name: Cassioli - first_name: Eliseo F. full_name: Castillo, Eliseo F. last_name: Castillo - first_name: Karen full_name: Castillo, Karen last_name: Castillo - first_name: Sonia full_name: Castillo-Lluva, Sonia last_name: Castillo-Lluva - first_name: Francesca full_name: Castoldi, Francesca last_name: Castoldi - first_name: Marco full_name: Castori, Marco last_name: Castori - first_name: Ariel F. full_name: Castro, Ariel F. last_name: Castro - first_name: Margarida full_name: Castro-Caldas, Margarida last_name: Castro-Caldas - first_name: Javier full_name: Castro-Hernandez, Javier last_name: Castro-Hernandez - first_name: Susana full_name: Castro-Obregon, Susana last_name: Castro-Obregon - first_name: Sergio D. full_name: Catz, Sergio D. last_name: Catz - first_name: Claudia full_name: Cavadas, Claudia last_name: Cavadas - first_name: Federica full_name: Cavaliere, Federica last_name: Cavaliere - first_name: Gabriella full_name: Cavallini, Gabriella last_name: Cavallini - first_name: Maria full_name: Cavinato, Maria last_name: Cavinato - first_name: Maria L. full_name: Cayuela, Maria L. last_name: Cayuela - first_name: Paula full_name: Cebollada Rica, Paula last_name: Cebollada Rica - first_name: Valentina full_name: Cecarini, Valentina last_name: Cecarini - first_name: Francesco full_name: Cecconi, Francesco last_name: Cecconi - first_name: Marzanna full_name: Cechowska-Pasko, Marzanna last_name: Cechowska-Pasko - first_name: Simone full_name: Cenci, Simone last_name: Cenci - first_name: Victòria full_name: Ceperuelo-Mallafré, Victòria last_name: Ceperuelo-Mallafré - first_name: João J. full_name: Cerqueira, João J. last_name: Cerqueira - first_name: Janete M. full_name: Cerutti, Janete M. last_name: Cerutti - first_name: Davide full_name: Cervia, Davide last_name: Cervia - first_name: Vildan Bozok full_name: Cetintas, Vildan Bozok last_name: Cetintas - first_name: Silvia full_name: Cetrullo, Silvia last_name: Cetrullo - first_name: Han Jung full_name: Chae, Han Jung last_name: Chae - first_name: Andrei S. full_name: Chagin, Andrei S. last_name: Chagin - first_name: Chee Yin full_name: Chai, Chee Yin last_name: Chai - first_name: Gopal full_name: Chakrabarti, Gopal last_name: Chakrabarti - first_name: Oishee full_name: Chakrabarti, Oishee last_name: Chakrabarti - first_name: Tapas full_name: Chakraborty, Tapas last_name: Chakraborty - first_name: Trinad full_name: Chakraborty, Trinad last_name: Chakraborty - first_name: Mounia full_name: Chami, Mounia last_name: Chami - first_name: Georgios full_name: Chamilos, Georgios last_name: Chamilos - first_name: David W. full_name: Chan, David W. last_name: Chan - first_name: Edmond Y.W. full_name: Chan, Edmond Y.W. last_name: Chan - first_name: Edward D. full_name: Chan, Edward D. last_name: Chan - first_name: H. 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first_name: Santosh full_name: Chauhan, Santosh last_name: Chauhan - first_name: Edward full_name: Chaum, Edward last_name: Chaum - first_name: Frédéric full_name: Checler, Frédéric last_name: Checler - first_name: Michael E. full_name: Cheetham, Michael E. last_name: Cheetham - first_name: Chang Shi full_name: Chen, Chang Shi last_name: Chen - first_name: Guang Chao full_name: Chen, Guang Chao last_name: Chen - first_name: Jian Fu full_name: Chen, Jian Fu last_name: Chen - first_name: Liam L. full_name: Chen, Liam L. last_name: Chen - first_name: Leilei full_name: Chen, Leilei last_name: Chen - first_name: Lin full_name: Chen, Lin last_name: Chen - first_name: Mingliang full_name: Chen, Mingliang last_name: Chen - first_name: Mu Kuan full_name: Chen, Mu Kuan last_name: Chen - first_name: Ning full_name: Chen, Ning last_name: Chen - first_name: Quan full_name: Chen, Quan last_name: Chen - first_name: Ruey Hwa full_name: Chen, Ruey Hwa last_name: Chen - first_name: Shi full_name: Chen, Shi last_name: Chen - first_name: Wei full_name: Chen, Wei last_name: Chen - first_name: Weiqiang full_name: Chen, Weiqiang last_name: Chen - first_name: Xin Ming full_name: Chen, Xin Ming last_name: Chen - first_name: Xiong Wen full_name: Chen, Xiong Wen last_name: Chen - first_name: Xu full_name: Chen, Xu id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87 last_name: Chen - first_name: Yan full_name: Chen, Yan last_name: Chen - first_name: Ye Guang full_name: Chen, Ye Guang last_name: Chen - first_name: Yingyu full_name: Chen, Yingyu last_name: Chen - first_name: Yongqiang full_name: Chen, Yongqiang last_name: Chen - first_name: Yu Jen full_name: Chen, Yu Jen last_name: Chen - first_name: Yue Qin full_name: Chen, Yue Qin last_name: Chen - first_name: Zhefan Stephen full_name: Chen, Zhefan Stephen last_name: Chen - first_name: Zhi full_name: Chen, Zhi last_name: Chen - first_name: Zhi Hua full_name: Chen, Zhi Hua last_name: Chen - first_name: Zhijian J. full_name: Chen, Zhijian J. last_name: Chen - first_name: Zhixiang full_name: Chen, Zhixiang last_name: Chen - first_name: Hanhua full_name: Cheng, Hanhua last_name: Cheng - first_name: Jun full_name: Cheng, Jun last_name: Cheng - first_name: Shi Yuan full_name: Cheng, Shi Yuan last_name: Cheng - first_name: Wei full_name: Cheng, Wei last_name: Cheng - first_name: Xiaodong full_name: Cheng, Xiaodong last_name: Cheng - first_name: Xiu Tang full_name: Cheng, Xiu Tang last_name: Cheng - first_name: Yiyun full_name: Cheng, Yiyun last_name: Cheng - first_name: Zhiyong full_name: Cheng, Zhiyong last_name: Cheng - first_name: Zhong full_name: Chen, Zhong last_name: Chen - first_name: Heesun full_name: Cheong, Heesun last_name: Cheong - first_name: Jit Kong full_name: Cheong, Jit Kong last_name: Cheong - first_name: Boris V. full_name: Chernyak, Boris V. last_name: Chernyak - first_name: Sara full_name: Cherry, Sara last_name: Cherry - first_name: Chi Fai Randy full_name: Cheung, Chi Fai Randy last_name: Cheung - first_name: Chun Hei Antonio full_name: Cheung, Chun Hei Antonio last_name: Cheung - first_name: King Ho full_name: Cheung, King Ho last_name: Cheung - first_name: Eric full_name: Chevet, Eric last_name: Chevet - first_name: Richard J. full_name: Chi, Richard J. last_name: Chi - first_name: Alan Kwok Shing full_name: Chiang, Alan Kwok Shing last_name: Chiang - first_name: Ferdinando full_name: Chiaradonna, Ferdinando last_name: Chiaradonna - first_name: Roberto full_name: Chiarelli, Roberto last_name: Chiarelli - first_name: Mario full_name: Chiariello, Mario last_name: Chiariello - first_name: Nathalia full_name: Chica, Nathalia last_name: Chica - first_name: Susanna full_name: Chiocca, Susanna last_name: Chiocca - first_name: Mario full_name: Chiong, Mario last_name: Chiong - first_name: Shih Hwa full_name: Chiou, Shih Hwa last_name: Chiou - first_name: Abhilash I. full_name: Chiramel, Abhilash I. last_name: Chiramel - first_name: Valerio full_name: Chiurchiù, Valerio last_name: Chiurchiù - first_name: Dong Hyung full_name: Cho, Dong Hyung last_name: Cho - first_name: Seong Kyu full_name: Choe, Seong Kyu last_name: Choe - first_name: Augustine M.K. full_name: Choi, Augustine M.K. last_name: Choi - first_name: Mary E. full_name: Choi, Mary E. last_name: Choi - first_name: Kamalika Roy full_name: Choudhury, Kamalika Roy last_name: Choudhury - first_name: Norman S. full_name: Chow, Norman S. last_name: Chow - first_name: Charleen T. full_name: Chu, Charleen T. last_name: Chu - first_name: Jason P. full_name: Chua, Jason P. last_name: Chua - first_name: John Jia En full_name: Chua, John Jia En last_name: Chua - first_name: Hyewon full_name: Chung, Hyewon last_name: Chung - first_name: Kin Pan full_name: Chung, Kin Pan last_name: Chung - first_name: Seockhoon full_name: Chung, Seockhoon last_name: Chung - first_name: So Hyang full_name: Chung, So Hyang last_name: Chung - first_name: Yuen Li full_name: Chung, Yuen Li last_name: Chung - first_name: Valentina full_name: Cianfanelli, Valentina last_name: Cianfanelli - first_name: Iwona A. full_name: Ciechomska, Iwona A. last_name: Ciechomska - first_name: Mariana full_name: Cifuentes, Mariana last_name: Cifuentes - first_name: Laura full_name: Cinque, Laura last_name: Cinque - 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first_name: Dale P. full_name: Corkery, Dale P. last_name: Corkery - first_name: Nils full_name: Cordes, Nils last_name: Cordes - first_name: Katia full_name: Cortese, Katia last_name: Cortese - first_name: Maria Do Carmo full_name: Costa, Maria Do Carmo last_name: Costa - first_name: Sarah full_name: Costantino, Sarah last_name: Costantino - first_name: Paola full_name: Costelli, Paola last_name: Costelli - first_name: Ana full_name: Coto-Montes, Ana last_name: Coto-Montes - first_name: Peter J. full_name: Crack, Peter J. last_name: Crack - first_name: Jose L. full_name: Crespo, Jose L. last_name: Crespo - first_name: Alfredo full_name: Criollo, Alfredo last_name: Criollo - first_name: Valeria full_name: Crippa, Valeria last_name: Crippa - first_name: Riccardo full_name: Cristofani, Riccardo last_name: Cristofani - first_name: Tamas full_name: Csizmadia, Tamas last_name: Csizmadia - first_name: Antonio full_name: Cuadrado, Antonio last_name: Cuadrado - first_name: Bing full_name: Cui, Bing last_name: Cui - 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first_name: Chiara full_name: De Leonibus, Chiara last_name: De Leonibus - first_name: Mayara G. full_name: De Mattos Barbosa, Mayara G. last_name: De Mattos Barbosa - first_name: Guido R.Y. full_name: De Meyer, Guido R.Y. last_name: De Meyer - first_name: Angelo full_name: De Milito, Angelo last_name: De Milito - first_name: Cosimo full_name: De Nunzio, Cosimo last_name: De Nunzio - first_name: Clara full_name: De Palma, Clara last_name: De Palma - first_name: Mauro full_name: De Santi, Mauro last_name: De Santi - first_name: Claudio full_name: De Virgilio, Claudio last_name: De Virgilio - first_name: Daniela full_name: De Zio, Daniela last_name: De Zio - first_name: Jayanta full_name: Debnath, Jayanta last_name: Debnath - first_name: Brian J. full_name: Debosch, Brian J. last_name: Debosch - first_name: Jean Paul full_name: Decuypere, Jean Paul last_name: Decuypere - first_name: Mark A. full_name: Deehan, Mark A. last_name: Deehan - first_name: Gianluca full_name: Deflorian, Gianluca last_name: Deflorian - first_name: James full_name: Degregori, James last_name: Degregori - first_name: Benjamin full_name: Dehay, Benjamin last_name: Dehay - first_name: Gabriel full_name: Del Rio, Gabriel last_name: Del Rio - first_name: Joe R. full_name: Delaney, Joe R. last_name: Delaney - first_name: Lea M.D. full_name: Delbridge, Lea M.D. last_name: Delbridge - first_name: Elizabeth full_name: Delorme-Axford, Elizabeth last_name: Delorme-Axford - first_name: M. 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first_name: Grant full_name: Dewson, Grant last_name: Dewson - first_name: Mahendiran full_name: Dharmasivam, Mahendiran last_name: Dharmasivam - first_name: Rohan full_name: Dhiman, Rohan last_name: Dhiman - first_name: Diego full_name: Di Bernardo, Diego last_name: Di Bernardo - first_name: Manlio full_name: Di Cristina, Manlio last_name: Di Cristina - first_name: Fabio full_name: Di Domenico, Fabio last_name: Di Domenico - first_name: Pietro full_name: Di Fazio, Pietro last_name: Di Fazio - first_name: Alessio full_name: Di Fonzo, Alessio last_name: Di Fonzo - first_name: Giovanni full_name: Di Guardo, Giovanni last_name: Di Guardo - first_name: Gianni M. full_name: Di Guglielmo, Gianni M. last_name: Di Guglielmo - first_name: Luca full_name: Di Leo, Luca last_name: Di Leo - first_name: Chiara full_name: Di Malta, Chiara last_name: Di Malta - first_name: Alessia full_name: Di Nardo, Alessia last_name: Di Nardo - first_name: Martina full_name: Di Rienzo, Martina last_name: Di Rienzo - first_name: Federica full_name: Di Sano, Federica last_name: Di Sano - first_name: George full_name: Diallinas, George last_name: Diallinas - first_name: Jiajie full_name: Diao, Jiajie last_name: Diao - first_name: Guillermo full_name: Diaz-Araya, Guillermo last_name: Diaz-Araya - first_name: Inés full_name: Díaz-Laviada, Inés last_name: Díaz-Laviada - first_name: Jared M. full_name: Dickinson, Jared M. last_name: Dickinson - first_name: Marc full_name: Diederich, Marc last_name: Diederich - first_name: Mélanie full_name: Dieudé, Mélanie last_name: Dieudé - first_name: Ivan full_name: Dikic, Ivan last_name: Dikic - first_name: Shiping full_name: Ding, Shiping last_name: Ding - first_name: Wen Xing full_name: Ding, Wen Xing last_name: Ding - first_name: Luciana full_name: Dini, Luciana last_name: Dini - first_name: Jelena full_name: Dinić, Jelena last_name: Dinić - first_name: Miroslav full_name: Dinic, Miroslav last_name: Dinic - first_name: Albena T. full_name: Dinkova-Kostova, Albena T. last_name: Dinkova-Kostova - first_name: Marc S. full_name: Dionne, Marc S. last_name: Dionne - first_name: Jörg H.W. full_name: Distler, Jörg H.W. last_name: Distler - first_name: Abhinav full_name: Diwan, Abhinav last_name: Diwan - first_name: Ian M.C. full_name: Dixon, Ian M.C. last_name: Dixon - first_name: Mojgan full_name: Djavaheri-Mergny, Mojgan last_name: Djavaheri-Mergny - first_name: Ina full_name: Dobrinski, Ina last_name: Dobrinski - first_name: Oxana full_name: Dobrovinskaya, Oxana last_name: Dobrovinskaya - first_name: Radek full_name: Dobrowolski, Radek last_name: Dobrowolski - first_name: Renwick C.J. full_name: Dobson, Renwick C.J. last_name: Dobson - first_name: Jelena full_name: Đokić, Jelena last_name: Đokić - first_name: Serap full_name: Dokmeci Emre, Serap last_name: Dokmeci Emre - first_name: Massimo full_name: Donadelli, Massimo last_name: Donadelli - first_name: Bo full_name: Dong, Bo last_name: Dong - first_name: Xiaonan full_name: Dong, Xiaonan last_name: Dong - first_name: Zhiwu full_name: Dong, Zhiwu last_name: Dong - first_name: Gerald W. full_name: Dorn, Gerald W. last_name: Dorn - first_name: Volker full_name: Dotsch, Volker last_name: Dotsch - first_name: Huan full_name: Dou, Huan last_name: Dou - first_name: Juan full_name: Dou, Juan last_name: Dou - first_name: Moataz full_name: Dowaidar, Moataz last_name: Dowaidar - first_name: Sami full_name: Dridi, Sami last_name: Dridi - first_name: Liat full_name: Drucker, Liat last_name: Drucker - first_name: Ailian full_name: Du, Ailian last_name: Du - first_name: Caigan full_name: Du, Caigan last_name: Du - first_name: Guangwei full_name: Du, Guangwei last_name: Du - first_name: Hai Ning full_name: Du, Hai Ning last_name: Du - first_name: Li Lin full_name: Du, Li Lin last_name: Du - first_name: André full_name: Du Toit, André last_name: Du Toit - first_name: Shao Bin full_name: Duan, Shao Bin last_name: Duan - first_name: Xiaoqiong full_name: Duan, Xiaoqiong last_name: Duan - first_name: Sónia P. full_name: Duarte, Sónia P. last_name: Duarte - first_name: Anna full_name: Dubrovska, Anna last_name: Dubrovska - first_name: Elaine A. full_name: Dunlop, Elaine A. last_name: Dunlop - first_name: Nicolas full_name: Dupont, Nicolas last_name: Dupont - first_name: Raúl V. full_name: Durán, Raúl V. last_name: Durán - first_name: Bilikere S. full_name: Dwarakanath, Bilikere S. last_name: Dwarakanath - first_name: Sergey A. full_name: Dyshlovoy, Sergey A. last_name: Dyshlovoy - first_name: Darius full_name: Ebrahimi-Fakhari, Darius last_name: Ebrahimi-Fakhari - first_name: Leopold full_name: Eckhart, Leopold last_name: Eckhart - first_name: Charles L. full_name: Edelstein, Charles L. last_name: Edelstein - first_name: Thomas full_name: Efferth, Thomas last_name: Efferth - first_name: Eftekhar full_name: Eftekharpour, Eftekhar last_name: Eftekharpour - first_name: Ludwig full_name: Eichinger, Ludwig last_name: Eichinger - first_name: Nabil full_name: Eid, Nabil last_name: Eid - first_name: Tobias full_name: Eisenberg, Tobias last_name: Eisenberg - first_name: N. 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first_name: Jiachun full_name: Feng, Jiachun last_name: Feng - first_name: Lifeng full_name: Feng, Lifeng last_name: Feng - first_name: Yibin full_name: Feng, Yibin last_name: Feng - first_name: Yuchen full_name: Feng, Yuchen last_name: Feng - first_name: Wei full_name: Feng, Wei last_name: Feng - first_name: Thais full_name: Fenz Araujo, Thais last_name: Fenz Araujo - first_name: Thomas A. full_name: Ferguson, Thomas A. last_name: Ferguson - first_name: Álvaro F. full_name: Fernández, Álvaro F. last_name: Fernández - first_name: Jose C. full_name: Fernandez-Checa, Jose C. last_name: Fernandez-Checa - first_name: Sonia full_name: Fernández-Veledo, Sonia last_name: Fernández-Veledo - first_name: Alisdair R. full_name: Fernie, Alisdair R. last_name: Fernie - first_name: Anthony W. full_name: Ferrante, Anthony W. last_name: Ferrante - first_name: Alessandra full_name: Ferraresi, Alessandra last_name: Ferraresi - first_name: Merari F. full_name: Ferrari, Merari F. last_name: Ferrari - first_name: Julio C.B. full_name: Ferreira, Julio C.B. last_name: Ferreira - first_name: Susan full_name: Ferro-Novick, Susan last_name: Ferro-Novick - first_name: Antonio full_name: Figueras, Antonio last_name: Figueras - first_name: Riccardo full_name: Filadi, Riccardo last_name: Filadi - first_name: Nicoletta full_name: Filigheddu, Nicoletta last_name: Filigheddu - first_name: Eduardo full_name: Filippi-Chiela, Eduardo last_name: Filippi-Chiela - first_name: Giuseppe full_name: Filomeni, Giuseppe last_name: Filomeni - first_name: Gian Maria full_name: Fimia, Gian Maria last_name: Fimia - first_name: Vittorio full_name: Fineschi, Vittorio last_name: Fineschi - first_name: Francesca full_name: Finetti, Francesca last_name: Finetti - first_name: Steven full_name: Finkbeiner, Steven last_name: Finkbeiner - first_name: Edward A. full_name: Fisher, Edward A. last_name: Fisher - first_name: Paul B. full_name: Fisher, Paul B. last_name: Fisher - first_name: Flavio full_name: Flamigni, Flavio last_name: Flamigni - first_name: Steven J. full_name: Fliesler, Steven J. last_name: Fliesler - first_name: Trude H. full_name: Flo, Trude H. last_name: Flo - first_name: Ida full_name: Florance, Ida last_name: Florance - first_name: Oliver full_name: Florey, Oliver last_name: Florey - first_name: Tullio full_name: Florio, Tullio last_name: Florio - first_name: Erika full_name: Fodor, Erika last_name: Fodor - first_name: Carlo full_name: Follo, Carlo last_name: Follo - first_name: Edward A. full_name: Fon, Edward A. last_name: Fon - first_name: Antonella full_name: Forlino, Antonella last_name: Forlino - first_name: Francesco full_name: Fornai, Francesco last_name: Fornai - first_name: Paola full_name: Fortini, Paola last_name: Fortini - first_name: Anna full_name: Fracassi, Anna last_name: Fracassi - first_name: Alessandro full_name: Fraldi, Alessandro last_name: Fraldi - first_name: Brunella full_name: Franco, Brunella last_name: Franco - first_name: Rodrigo full_name: Franco, Rodrigo last_name: Franco - first_name: Flavia full_name: Franconi, Flavia last_name: Franconi - first_name: Lisa B. full_name: Frankel, Lisa B. last_name: Frankel - 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first_name: Alessia full_name: Galasso, Alessia last_name: Galasso - first_name: Maria F. full_name: Galindo, Maria F. last_name: Galindo - first_name: Sachith full_name: Gallolu Kankanamalage, Sachith last_name: Gallolu Kankanamalage - first_name: Lorenzo full_name: Galluzzi, Lorenzo last_name: Galluzzi - first_name: Vincent full_name: Galy, Vincent last_name: Galy - first_name: Noor full_name: Gammoh, Noor last_name: Gammoh - first_name: Boyi full_name: Gan, Boyi last_name: Gan - first_name: Ian G. full_name: Ganley, Ian G. last_name: Ganley - first_name: Feng full_name: Gao, Feng last_name: Gao - first_name: Hui full_name: Gao, Hui last_name: Gao - first_name: Minghui full_name: Gao, Minghui last_name: Gao - first_name: Ping full_name: Gao, Ping last_name: Gao - first_name: Shou Jiang full_name: Gao, Shou Jiang last_name: Gao - first_name: Wentao full_name: Gao, Wentao last_name: Gao - first_name: Xiaobo full_name: Gao, Xiaobo last_name: Gao - first_name: Ana full_name: Garcera, Ana last_name: Garcera - first_name: Maria Noé full_name: Garcia, Maria Noé last_name: Garcia - first_name: Verónica E. full_name: Garcia, Verónica E. last_name: Garcia - first_name: Francisco full_name: García-Del Portillo, Francisco last_name: García-Del Portillo - first_name: Vega full_name: Garcia-Escudero, Vega last_name: Garcia-Escudero - first_name: Aracely full_name: Garcia-Garcia, Aracely last_name: Garcia-Garcia - first_name: Marina full_name: Garcia-Macia, Marina last_name: Garcia-Macia - first_name: Diana full_name: García-Moreno, Diana last_name: García-Moreno - first_name: Carmen full_name: Garcia-Ruiz, Carmen last_name: Garcia-Ruiz - first_name: Patricia full_name: García-Sanz, Patricia last_name: García-Sanz - first_name: Abhishek D. full_name: Garg, Abhishek D. last_name: Garg - first_name: Ricardo full_name: Gargini, Ricardo last_name: Gargini - first_name: Tina full_name: Garofalo, Tina last_name: Garofalo - first_name: Robert F. full_name: Garry, Robert F. last_name: Garry - first_name: Nils C. full_name: Gassen, Nils C. last_name: Gassen - 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first_name: Manosij full_name: Ghosh, Manosij last_name: Ghosh - first_name: Georgios full_name: Giamas, Georgios last_name: Giamas - first_name: Claudia full_name: Giampietri, Claudia last_name: Giampietri - first_name: Alexandra full_name: Giatromanolaki, Alexandra last_name: Giatromanolaki - first_name: Gary E. full_name: Gibson, Gary E. last_name: Gibson - first_name: Spencer B. full_name: Gibson, Spencer B. last_name: Gibson - first_name: Vanessa full_name: Ginet, Vanessa last_name: Ginet - first_name: Edward full_name: Giniger, Edward last_name: Giniger - first_name: Carlotta full_name: Giorgi, Carlotta last_name: Giorgi - first_name: Henrique full_name: Girao, Henrique last_name: Girao - first_name: Stephen E. full_name: Girardin, Stephen E. last_name: Girardin - first_name: Mridhula full_name: Giridharan, Mridhula last_name: Giridharan - first_name: Sandy full_name: Giuliano, Sandy last_name: Giuliano - first_name: Cecilia full_name: Giulivi, Cecilia last_name: Giulivi - first_name: Sylvie full_name: Giuriato, Sylvie last_name: Giuriato - first_name: Julien full_name: Giustiniani, Julien last_name: Giustiniani - first_name: Alexander full_name: Gluschko, Alexander last_name: Gluschko - first_name: Veit full_name: Goder, Veit last_name: Goder - first_name: Alexander full_name: Goginashvili, Alexander last_name: Goginashvili - first_name: Jakub full_name: Golab, Jakub last_name: Golab - first_name: David C. full_name: Goldstone, David C. last_name: Goldstone - first_name: Anna full_name: Golebiewska, Anna last_name: Golebiewska - first_name: Luciana R. full_name: Gomes, Luciana R. last_name: Gomes - first_name: Rodrigo full_name: Gomez, Rodrigo last_name: Gomez - first_name: Rubén full_name: Gómez-Sánchez, Rubén last_name: Gómez-Sánchez - first_name: Maria Catalina full_name: Gomez-Puerto, Maria Catalina last_name: Gomez-Puerto - first_name: Raquel full_name: Gomez-Sintes, Raquel last_name: Gomez-Sintes - first_name: Qingqiu full_name: Gong, Qingqiu last_name: Gong - first_name: Felix M. full_name: Goni, Felix M. last_name: Goni - 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first_name: Nirmala full_name: Hariharan, Nirmala last_name: Hariharan - first_name: Nigil full_name: Haroon, Nigil last_name: Haroon - first_name: James full_name: Harris, James last_name: Harris - first_name: Takafumi full_name: Hasegawa, Takafumi last_name: Hasegawa - first_name: Noor full_name: Hasima Nagoor, Noor last_name: Hasima Nagoor - first_name: Jeffrey A. full_name: Haspel, Jeffrey A. last_name: Haspel - first_name: Volker full_name: Haucke, Volker last_name: Haucke - first_name: Wayne D. full_name: Hawkins, Wayne D. last_name: Hawkins - first_name: Bruce A. full_name: Hay, Bruce A. last_name: Hay - first_name: Cole M. full_name: Haynes, Cole M. last_name: Haynes - first_name: Soren B. full_name: Hayrabedyan, Soren B. last_name: Hayrabedyan - first_name: Thomas S. full_name: Hays, Thomas S. last_name: Hays - first_name: Congcong full_name: He, Congcong last_name: He - first_name: Qin full_name: He, Qin last_name: He - first_name: Rong Rong full_name: He, Rong Rong last_name: He - 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first_name: José M. full_name: Izquierdo, José M. last_name: Izquierdo - first_name: Masanori full_name: Izumi, Masanori last_name: Izumi - first_name: Marja full_name: Jäättelä, Marja last_name: Jäättelä - first_name: Majid Sakhi full_name: Jabir, Majid Sakhi last_name: Jabir - first_name: William T. full_name: Jackson, William T. last_name: Jackson - first_name: Nadia full_name: Jacobo-Herrera, Nadia last_name: Jacobo-Herrera - first_name: Anne Claire full_name: Jacomin, Anne Claire last_name: Jacomin - first_name: Elise full_name: Jacquin, Elise last_name: Jacquin - first_name: Pooja full_name: Jadiya, Pooja last_name: Jadiya - first_name: Hartmut full_name: Jaeschke, Hartmut last_name: Jaeschke - first_name: Chinnaswamy full_name: Jagannath, Chinnaswamy last_name: Jagannath - first_name: Arjen J. full_name: Jakobi, Arjen J. last_name: Jakobi - first_name: Johan full_name: Jakobsson, Johan last_name: Jakobsson - first_name: Bassam full_name: Janji, Bassam last_name: Janji - first_name: Pidder full_name: Jansen-Dürr, Pidder last_name: Jansen-Dürr - 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first_name: Dimitri full_name: Krainc, Dimitri last_name: Krainc - first_name: Helmut full_name: Krämer, Helmut last_name: Krämer - first_name: Anna D. full_name: Krasnodembskaya, Anna D. last_name: Krasnodembskaya - first_name: Carole full_name: Kretz-Remy, Carole last_name: Kretz-Remy - first_name: Guido full_name: Kroemer, Guido last_name: Kroemer - first_name: Nicholas T. full_name: Ktistakis, Nicholas T. last_name: Ktistakis - first_name: Kazuyuki full_name: Kuchitsu, Kazuyuki last_name: Kuchitsu - first_name: Sabine full_name: Kuenen, Sabine last_name: Kuenen - first_name: Lars full_name: Kuerschner, Lars last_name: Kuerschner - first_name: Thomas full_name: Kukar, Thomas last_name: Kukar - first_name: Ajay full_name: Kumar, Ajay last_name: Kumar - first_name: Ashok full_name: Kumar, Ashok last_name: Kumar - first_name: Deepak full_name: Kumar, Deepak last_name: Kumar - first_name: Dhiraj full_name: Kumar, Dhiraj last_name: Kumar - first_name: Sharad full_name: Kumar, Sharad last_name: Kumar - 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first_name: Sylvain full_name: Ladoire, Sylvain last_name: Ladoire - first_name: Ilaria full_name: Laface, Ilaria last_name: Laface - first_name: Frank full_name: Lafont, Frank last_name: Lafont - first_name: Diane C. full_name: Lagace, Diane C. last_name: Lagace - first_name: Vikramjit full_name: Lahiri, Vikramjit last_name: Lahiri - first_name: Zhibing full_name: Lai, Zhibing last_name: Lai - first_name: Angela S. full_name: Laird, Angela S. last_name: Laird - first_name: Aparna full_name: Lakkaraju, Aparna last_name: Lakkaraju - first_name: Trond full_name: Lamark, Trond last_name: Lamark - first_name: Sheng Hui full_name: Lan, Sheng Hui last_name: Lan - first_name: Ane full_name: Landajuela, Ane last_name: Landajuela - first_name: Darius J.R. full_name: Lane, Darius J.R. last_name: Lane - first_name: Jon D. full_name: Lane, Jon D. last_name: Lane - first_name: Charles H. full_name: Lang, Charles H. last_name: Lang - first_name: Carsten full_name: Lange, Carsten last_name: Lange - first_name: Ülo full_name: Langel, Ülo last_name: Langel - 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first_name: Lionel Y.W. full_name: Leck, Lionel Y.W. last_name: Leck - first_name: Jean Philippe full_name: Leduc-Gaudet, Jean Philippe last_name: Leduc-Gaudet - first_name: Changwook full_name: Lee, Changwook last_name: Lee - first_name: Chung Pei full_name: Lee, Chung Pei last_name: Lee - first_name: Da Hye full_name: Lee, Da Hye last_name: Lee - first_name: Edward B. full_name: Lee, Edward B. last_name: Lee - first_name: Erinna F. full_name: Lee, Erinna F. last_name: Lee - first_name: Gyun Min full_name: Lee, Gyun Min last_name: Lee - first_name: He Jin full_name: Lee, He Jin last_name: Lee - first_name: Heung Kyu full_name: Lee, Heung Kyu last_name: Lee - first_name: Jae Man full_name: Lee, Jae Man last_name: Lee - first_name: Jason S. full_name: Lee, Jason S. last_name: Lee - first_name: Jin A. full_name: Lee, Jin A. last_name: Lee - first_name: Joo Yong full_name: Lee, Joo Yong last_name: Lee - first_name: Jun Hee full_name: Lee, Jun Hee last_name: Lee - first_name: Michael full_name: Lee, Michael last_name: Lee - 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first_name: Honglin full_name: Luo, Honglin last_name: Luo - first_name: Rongcan full_name: Luo, Rongcan last_name: Luo - first_name: Shouqing full_name: Luo, Shouqing last_name: Luo - first_name: Zhi full_name: Luo, Zhi last_name: Luo - first_name: Claudio full_name: Luparello, Claudio last_name: Luparello - first_name: Bernhard full_name: Lüscher, Bernhard last_name: Lüscher - first_name: Luan full_name: Luu, Luan last_name: Luu - first_name: Alex full_name: Lyakhovich, Alex last_name: Lyakhovich - first_name: Konstantin G. full_name: Lyamzaev, Konstantin G. last_name: Lyamzaev - first_name: Alf Håkon full_name: Lystad, Alf Håkon last_name: Lystad - first_name: Lyubomyr full_name: Lytvynchuk, Lyubomyr last_name: Lytvynchuk - first_name: Alvin C. full_name: Ma, Alvin C. last_name: Ma - first_name: Changle full_name: Ma, Changle last_name: Ma - first_name: Mengxiao full_name: Ma, Mengxiao last_name: Ma - first_name: Ning Fang full_name: Ma, Ning Fang last_name: Ma - first_name: Quan Hong full_name: Ma, Quan Hong last_name: Ma - first_name: Xinliang full_name: Ma, Xinliang last_name: Ma - first_name: Yueyun full_name: Ma, Yueyun last_name: Ma - first_name: Zhenyi full_name: Ma, Zhenyi last_name: Ma - first_name: Ormond A. full_name: Macdougald, Ormond A. last_name: Macdougald - first_name: Fernando full_name: Macian, Fernando last_name: Macian - first_name: Gustavo C. full_name: Macintosh, Gustavo C. last_name: Macintosh - first_name: Jeffrey P. full_name: Mackeigan, Jeffrey P. last_name: Mackeigan - first_name: Kay F. full_name: Macleod, Kay F. last_name: Macleod - first_name: Sandra full_name: Maday, Sandra last_name: Maday - first_name: Frank full_name: Madeo, Frank last_name: Madeo - first_name: Muniswamy full_name: Madesh, Muniswamy last_name: Madesh - first_name: Tobias full_name: Madl, Tobias last_name: Madl - first_name: Julio full_name: Madrigal-Matute, Julio last_name: Madrigal-Matute - first_name: Akiko full_name: Maeda, Akiko last_name: Maeda - first_name: Yasuhiro full_name: Maejima, Yasuhiro last_name: Maejima - first_name: Marta full_name: Magarinos, Marta last_name: Magarinos - first_name: Poornima full_name: Mahavadi, Poornima last_name: Mahavadi - first_name: Emiliano full_name: Maiani, Emiliano last_name: Maiani - first_name: Kenneth full_name: Maiese, Kenneth last_name: Maiese - first_name: Panchanan full_name: Maiti, Panchanan last_name: Maiti - first_name: Maria Chiara full_name: Maiuri, Maria Chiara last_name: Maiuri - first_name: Barbara full_name: Majello, Barbara last_name: Majello - first_name: Michael B. full_name: Major, Michael B. last_name: Major - first_name: Elena full_name: Makareeva, Elena last_name: Makareeva - first_name: Fayaz full_name: Malik, Fayaz last_name: Malik - first_name: Karthik full_name: Mallilankaraman, Karthik last_name: Mallilankaraman - first_name: Walter full_name: Malorni, Walter last_name: Malorni - first_name: Alina full_name: Maloyan, Alina last_name: Maloyan - first_name: Najiba full_name: Mammadova, Najiba last_name: Mammadova - first_name: Gene Chi Wai full_name: Man, Gene Chi Wai last_name: Man - first_name: Federico full_name: Manai, Federico last_name: Manai - first_name: Joseph D. full_name: Mancias, Joseph D. last_name: Mancias - first_name: Eva Maria full_name: Mandelkow, Eva Maria last_name: Mandelkow - first_name: Michael A. full_name: Mandell, Michael A. last_name: Mandell - first_name: Angelo A. full_name: Manfredi, Angelo A. last_name: Manfredi - first_name: Masoud H. full_name: Manjili, Masoud H. last_name: Manjili - first_name: Ravi full_name: Manjithaya, Ravi last_name: Manjithaya - first_name: Patricio full_name: Manque, Patricio last_name: Manque - first_name: Bella B. full_name: Manshian, Bella B. last_name: Manshian - first_name: Raquel full_name: Manzano, Raquel last_name: Manzano - first_name: Claudia full_name: Manzoni, Claudia last_name: Manzoni - first_name: Kai full_name: Mao, Kai last_name: Mao - first_name: Cinzia full_name: Marchese, Cinzia last_name: Marchese - first_name: Sandrine full_name: Marchetti, Sandrine last_name: Marchetti - first_name: Anna Maria full_name: Marconi, Anna Maria last_name: Marconi - first_name: Fabrizio full_name: Marcucci, Fabrizio last_name: Marcucci - first_name: Stefania full_name: Mardente, Stefania last_name: Mardente - first_name: Olga A. full_name: Mareninova, Olga A. last_name: Mareninova - first_name: Marta full_name: Margeta, Marta last_name: Margeta - first_name: Muriel full_name: Mari, Muriel last_name: Mari - first_name: Sara full_name: Marinelli, Sara last_name: Marinelli - first_name: Oliviero full_name: Marinelli, Oliviero last_name: Marinelli - first_name: Guillermo full_name: Mariño, Guillermo last_name: Mariño - first_name: Sofia full_name: Mariotto, Sofia last_name: Mariotto - first_name: Richard S. full_name: Marshall, Richard S. last_name: Marshall - first_name: Mark R. full_name: Marten, Mark R. last_name: Marten - first_name: Sascha full_name: Martens, Sascha last_name: Martens - first_name: Alexandre P.J. full_name: Martin, Alexandre P.J. last_name: Martin - first_name: Katie R. full_name: Martin, Katie R. last_name: Martin - first_name: Sara full_name: Martin, Sara last_name: Martin - first_name: Shaun full_name: Martin, Shaun last_name: Martin - first_name: Adrián full_name: Martín-Segura, Adrián last_name: Martín-Segura - first_name: Miguel A. full_name: Martín-Acebes, Miguel A. last_name: Martín-Acebes - first_name: Inmaculada full_name: Martin-Burriel, Inmaculada last_name: Martin-Burriel - first_name: Marcos full_name: Martin-Rincon, Marcos last_name: Martin-Rincon - first_name: Paloma full_name: Martin-Sanz, Paloma last_name: Martin-Sanz - first_name: José A. full_name: Martina, José A. last_name: Martina - first_name: Wim full_name: Martinet, Wim last_name: Martinet - first_name: Aitor full_name: Martinez, Aitor last_name: Martinez - first_name: Ana full_name: Martinez, Ana last_name: Martinez - first_name: Jennifer full_name: Martinez, Jennifer last_name: Martinez - first_name: Moises full_name: Martinez Velazquez, Moises last_name: Martinez Velazquez - first_name: Nuria full_name: Martinez-Lopez, Nuria last_name: Martinez-Lopez - first_name: Marta full_name: Martinez-Vicente, Marta last_name: Martinez-Vicente - first_name: Daniel O. full_name: Martins, Daniel O. last_name: Martins - first_name: Joilson O. full_name: Martins, Joilson O. last_name: Martins - first_name: Waleska K. full_name: Martins, Waleska K. last_name: Martins - first_name: Tania full_name: Martins-Marques, Tania last_name: Martins-Marques - first_name: Emanuele full_name: Marzetti, Emanuele last_name: Marzetti - first_name: Shashank full_name: Masaldan, Shashank last_name: Masaldan - first_name: Celine full_name: Masclaux-Daubresse, Celine last_name: Masclaux-Daubresse - first_name: Douglas G. full_name: Mashek, Douglas G. last_name: Mashek - first_name: Valentina full_name: Massa, Valentina last_name: Massa - first_name: Lourdes full_name: Massieu, Lourdes last_name: Massieu - first_name: Glenn R. full_name: Masson, Glenn R. last_name: Masson - first_name: Laura full_name: Masuelli, Laura last_name: Masuelli - first_name: Anatoliy I. full_name: Masyuk, Anatoliy I. last_name: Masyuk - first_name: Tetyana V. full_name: Masyuk, Tetyana V. last_name: Masyuk - first_name: Paola full_name: Matarrese, Paola last_name: Matarrese - first_name: Ander full_name: Matheu, Ander last_name: Matheu - first_name: Satoaki full_name: Matoba, Satoaki last_name: Matoba - first_name: Sachiko full_name: Matsuzaki, Sachiko last_name: Matsuzaki - first_name: Pamela full_name: Mattar, Pamela last_name: Mattar - first_name: Alessandro full_name: Matte, Alessandro last_name: Matte - first_name: Domenico full_name: Mattoscio, Domenico last_name: Mattoscio - first_name: José L. full_name: Mauriz, José L. last_name: Mauriz - first_name: Mario full_name: Mauthe, Mario last_name: Mauthe - first_name: Caroline full_name: Mauvezin, Caroline last_name: Mauvezin - first_name: Emanual full_name: Maverakis, Emanual last_name: Maverakis - first_name: Paola full_name: Maycotte, Paola last_name: Maycotte - first_name: Johanna full_name: Mayer, Johanna last_name: Mayer - first_name: Gianluigi full_name: Mazzoccoli, Gianluigi last_name: Mazzoccoli - first_name: Cristina full_name: Mazzoni, Cristina last_name: Mazzoni - first_name: Joseph R. full_name: Mazzulli, Joseph R. last_name: Mazzulli - first_name: Nami full_name: Mccarty, Nami last_name: Mccarty - first_name: Christine full_name: Mcdonald, Christine last_name: Mcdonald - first_name: Mitchell R. full_name: Mcgill, Mitchell R. last_name: Mcgill - first_name: Sharon L. full_name: Mckenna, Sharon L. last_name: Mckenna - first_name: Beth Ann full_name: Mclaughlin, Beth Ann last_name: Mclaughlin - first_name: Fionn full_name: Mcloughlin, Fionn last_name: Mcloughlin - first_name: Mark A. full_name: Mcniven, Mark A. last_name: Mcniven - first_name: Thomas G. full_name: Mcwilliams, Thomas G. last_name: Mcwilliams - first_name: Fatima full_name: Mechta-Grigoriou, Fatima last_name: Mechta-Grigoriou - first_name: Tania Catarina full_name: Medeiros, Tania Catarina last_name: Medeiros - first_name: Diego L. full_name: Medina, Diego L. last_name: Medina - first_name: Lynn A. full_name: Megeney, Lynn A. last_name: Megeney - first_name: Klara full_name: Megyeri, Klara last_name: Megyeri - 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first_name: Enrico full_name: Milan, Enrico last_name: Milan - first_name: Małgorzata full_name: Milczarek, Małgorzata last_name: Milczarek - first_name: Dana L. full_name: Miller, Dana L. last_name: Miller - first_name: Samuel I. full_name: Miller, Samuel I. last_name: Miller - first_name: Silke full_name: Miller, Silke last_name: Miller - first_name: Steven W. full_name: Millward, Steven W. last_name: Millward - first_name: Ira full_name: Milosevic, Ira last_name: Milosevic - first_name: Elena A. full_name: Minina, Elena A. last_name: Minina - first_name: Hamed full_name: Mirzaei, Hamed last_name: Mirzaei - first_name: Hamid Reza full_name: Mirzaei, Hamid Reza last_name: Mirzaei - first_name: Mehdi full_name: Mirzaei, Mehdi last_name: Mirzaei - first_name: Amit full_name: Mishra, Amit last_name: Mishra - first_name: Nandita full_name: Mishra, Nandita last_name: Mishra - first_name: Paras Kumar full_name: Mishra, Paras Kumar last_name: Mishra - first_name: Maja full_name: Misirkic Marjanovic, Maja last_name: Misirkic Marjanovic - first_name: Roberta full_name: Misasi, Roberta last_name: Misasi - first_name: Amit full_name: Misra, Amit last_name: Misra - first_name: Gabriella full_name: Misso, Gabriella last_name: Misso - first_name: Claire full_name: Mitchell, Claire last_name: Mitchell - first_name: Geraldine full_name: Mitou, Geraldine last_name: Mitou - first_name: Tetsuji full_name: Miura, Tetsuji last_name: Miura - first_name: Shigeki full_name: Miyamoto, Shigeki last_name: Miyamoto - first_name: Makoto full_name: Miyazaki, Makoto last_name: Miyazaki - first_name: Mitsunori full_name: Miyazaki, Mitsunori last_name: Miyazaki - first_name: Taiga full_name: Miyazaki, Taiga last_name: Miyazaki - first_name: Keisuke full_name: Miyazawa, Keisuke last_name: Miyazawa - first_name: Noboru full_name: Mizushima, Noboru last_name: Mizushima - first_name: Trine H. full_name: Mogensen, Trine H. last_name: Mogensen - first_name: Baharia full_name: Mograbi, Baharia last_name: Mograbi - first_name: Reza full_name: Mohammadinejad, Reza last_name: Mohammadinejad - 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Patrick full_name: Murphy, J. 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Celeste full_name: Nicolao, M. 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Bishr full_name: Omary, M. 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first_name: Kinya full_name: Otsu, Kinya last_name: Otsu - first_name: Christiane full_name: Ott, Christiane last_name: Ott - first_name: Luisa full_name: Ottobrini, Luisa last_name: Ottobrini - first_name: Jing Hsiung James full_name: Ou, Jing Hsiung James last_name: Ou - first_name: Tiago F. full_name: Outeiro, Tiago F. last_name: Outeiro - first_name: Inger full_name: Oynebraten, Inger last_name: Oynebraten - first_name: Melek full_name: Ozturk, Melek last_name: Ozturk - first_name: Gilles full_name: Pagès, Gilles last_name: Pagès - first_name: Susanta full_name: Pahari, Susanta last_name: Pahari - first_name: Marta full_name: Pajares, Marta last_name: Pajares - first_name: Utpal B. full_name: Pajvani, Utpal B. last_name: Pajvani - first_name: Rituraj full_name: Pal, Rituraj last_name: Pal - first_name: Simona full_name: Paladino, Simona last_name: Paladino - first_name: Nicolas full_name: Pallet, Nicolas last_name: Pallet - first_name: Michela full_name: Palmieri, Michela last_name: Palmieri - first_name: Giuseppe full_name: Palmisano, Giuseppe last_name: Palmisano - first_name: Camilla full_name: Palumbo, Camilla last_name: Palumbo - first_name: Francesco full_name: Pampaloni, Francesco last_name: Pampaloni - first_name: Lifeng full_name: Pan, Lifeng last_name: Pan - first_name: Qingjun full_name: Pan, Qingjun last_name: Pan - first_name: Wenliang full_name: Pan, Wenliang last_name: Pan - first_name: Xin full_name: Pan, Xin last_name: Pan - first_name: Ganna full_name: Panasyuk, Ganna last_name: Panasyuk - first_name: Rahul full_name: Pandey, Rahul last_name: Pandey - first_name: Udai B. full_name: Pandey, Udai B. last_name: Pandey - first_name: Vrajesh full_name: Pandya, Vrajesh last_name: Pandya - first_name: Francesco full_name: Paneni, Francesco last_name: Paneni - first_name: Shirley Y. full_name: Pang, Shirley Y. last_name: Pang - first_name: Elisa full_name: Panzarini, Elisa last_name: Panzarini - first_name: Daniela L. full_name: Papademetrio, Daniela L. last_name: Papademetrio - first_name: Elena full_name: Papaleo, Elena last_name: Papaleo - first_name: Daniel full_name: Papinski, Daniel last_name: Papinski - first_name: Diana full_name: Papp, Diana last_name: Papp - first_name: Eun Chan full_name: Park, Eun Chan last_name: Park - first_name: Hwan Tae full_name: Park, Hwan Tae last_name: Park - first_name: Ji Man full_name: Park, Ji Man last_name: Park - first_name: Jong In full_name: Park, Jong In last_name: Park - first_name: Joon Tae full_name: Park, Joon Tae last_name: Park - first_name: Junsoo full_name: Park, Junsoo last_name: Park - first_name: Sang Chul full_name: Park, Sang Chul last_name: Park - first_name: Sang Youel full_name: Park, Sang Youel last_name: Park - first_name: Abraham H. full_name: Parola, Abraham H. last_name: Parola - first_name: Jan B. full_name: Parys, Jan B. last_name: Parys - first_name: Adrien full_name: Pasquier, Adrien last_name: Pasquier - first_name: Benoit full_name: Pasquier, Benoit last_name: Pasquier - first_name: João F. full_name: Passos, João F. last_name: Passos - first_name: Nunzia full_name: Pastore, Nunzia last_name: Pastore - first_name: Hemal H. full_name: Patel, Hemal H. last_name: Patel - first_name: Daniel full_name: Patschan, Daniel last_name: Patschan - first_name: Sophie full_name: Pattingre, Sophie last_name: Pattingre - first_name: Gustavo full_name: Pedraza-Alva, Gustavo last_name: Pedraza-Alva - first_name: Jose full_name: Pedraza-Chaverri, Jose last_name: Pedraza-Chaverri - first_name: Zully full_name: Pedrozo, Zully last_name: Pedrozo - first_name: Gang full_name: Pei, Gang last_name: Pei - first_name: Jianming full_name: Pei, Jianming last_name: Pei - first_name: Hadas full_name: Peled-Zehavi, Hadas last_name: Peled-Zehavi - first_name: Joaquín M. full_name: Pellegrini, Joaquín M. last_name: Pellegrini - first_name: Joffrey full_name: Pelletier, Joffrey last_name: Pelletier - first_name: Miguel A. full_name: Peñalva, Miguel A. last_name: Peñalva - first_name: Di full_name: Peng, Di last_name: Peng - first_name: Ying full_name: Peng, Ying last_name: Peng - first_name: Fabio full_name: Penna, Fabio last_name: Penna - first_name: Maria full_name: Pennuto, Maria last_name: Pennuto - first_name: Francesca full_name: Pentimalli, Francesca last_name: Pentimalli - first_name: Cláudia M.F. full_name: Pereira, Cláudia M.F. last_name: Pereira - first_name: Gustavo J.S. full_name: Pereira, Gustavo J.S. last_name: Pereira - first_name: Lilian C. full_name: Pereira, Lilian C. last_name: Pereira - first_name: Luis full_name: Pereira De Almeida, Luis last_name: Pereira De Almeida - first_name: Nirma D. full_name: Perera, Nirma D. last_name: Perera - first_name: Ángel full_name: Pérez-Lara, Ángel last_name: Pérez-Lara - first_name: Ana B. full_name: Perez-Oliva, Ana B. last_name: Perez-Oliva - first_name: María Esther full_name: Pérez-Pérez, María Esther last_name: Pérez-Pérez - first_name: Palsamy full_name: Periyasamy, Palsamy last_name: Periyasamy - first_name: Andras full_name: Perl, Andras last_name: Perl - first_name: Cristiana full_name: Perrotta, Cristiana last_name: Perrotta - 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first_name: Michael J. full_name: Ragusa, Michael J. last_name: Ragusa - first_name: Nader full_name: Rahimi, Nader last_name: Rahimi - first_name: Marveh full_name: Rahmati, Marveh last_name: Rahmati - first_name: Valeria full_name: Raia, Valeria last_name: Raia - first_name: Nuno full_name: Raimundo, Nuno last_name: Raimundo - first_name: Namakkal Soorappan full_name: Rajasekaran, Namakkal Soorappan last_name: Rajasekaran - first_name: Sriganesh full_name: Ramachandra Rao, Sriganesh last_name: Ramachandra Rao - first_name: Abdelhaq full_name: Rami, Abdelhaq last_name: Rami - first_name: Ignacio full_name: Ramírez-Pardo, Ignacio last_name: Ramírez-Pardo - first_name: David B. full_name: Ramsden, David B. last_name: Ramsden - first_name: Felix full_name: Randow, Felix last_name: Randow - first_name: Pundi N. full_name: Rangarajan, Pundi N. last_name: Rangarajan - first_name: Danilo full_name: Ranieri, Danilo last_name: Ranieri - first_name: Hai full_name: Rao, Hai last_name: Rao - first_name: Lang full_name: Rao, Lang last_name: Rao - first_name: Rekha full_name: Rao, Rekha last_name: Rao - first_name: Sumit full_name: Rathore, Sumit last_name: Rathore - first_name: J. Arjuna full_name: Ratnayaka, J. Arjuna last_name: Ratnayaka - first_name: Edward A. full_name: Ratovitski, Edward A. last_name: Ratovitski - first_name: Palaniyandi full_name: Ravanan, Palaniyandi last_name: Ravanan - first_name: Gloria full_name: Ravegnini, Gloria last_name: Ravegnini - first_name: Swapan K. full_name: Ray, Swapan K. last_name: Ray - first_name: Babak full_name: Razani, Babak last_name: Razani - first_name: Vito full_name: Rebecca, Vito last_name: Rebecca - first_name: Fulvio full_name: Reggiori, Fulvio last_name: Reggiori - first_name: Anne full_name: Régnier-Vigouroux, Anne last_name: Régnier-Vigouroux - first_name: Andreas S. full_name: Reichert, Andreas S. last_name: Reichert - first_name: David full_name: Reigada, David last_name: Reigada - first_name: Jan H. full_name: Reiling, Jan H. last_name: Reiling - first_name: Theo full_name: Rein, Theo last_name: Rein - first_name: Siegfried full_name: Reipert, Siegfried last_name: Reipert - first_name: Rokeya Sultana full_name: Rekha, Rokeya Sultana last_name: Rekha - first_name: Hongmei full_name: Ren, Hongmei last_name: Ren - first_name: Jun full_name: Ren, Jun last_name: Ren - first_name: Weichao full_name: Ren, Weichao last_name: Ren - first_name: Tristan full_name: Renault, Tristan last_name: Renault - first_name: Giorgia full_name: Renga, Giorgia last_name: Renga - first_name: Karen full_name: Reue, Karen last_name: Reue - first_name: Kim full_name: Rewitz, Kim last_name: Rewitz - first_name: Bruna full_name: Ribeiro De Andrade Ramos, Bruna last_name: Ribeiro De Andrade Ramos - first_name: S. Amer full_name: Riazuddin, S. Amer last_name: Riazuddin - first_name: Teresa M. full_name: Ribeiro-Rodrigues, Teresa M. last_name: Ribeiro-Rodrigues - first_name: Jean Ehrland full_name: Ricci, Jean Ehrland last_name: Ricci - first_name: Romeo full_name: Ricci, Romeo last_name: Ricci - first_name: Victoria full_name: Riccio, Victoria last_name: Riccio - first_name: Des R. full_name: Richardson, Des R. last_name: Richardson - first_name: Yasuko full_name: Rikihisa, Yasuko last_name: Rikihisa - first_name: Makarand V. full_name: Risbud, Makarand V. last_name: Risbud - first_name: Ruth M. full_name: Risueño, Ruth M. last_name: Risueño - first_name: Konstantinos full_name: Ritis, Konstantinos last_name: Ritis - first_name: Salvatore full_name: Rizza, Salvatore last_name: Rizza - first_name: Rosario full_name: Rizzuto, Rosario last_name: Rizzuto - first_name: Helen C. full_name: Roberts, Helen C. last_name: Roberts - first_name: Luke D. full_name: Roberts, Luke D. last_name: Roberts - first_name: Katherine J. full_name: Robinson, Katherine J. last_name: Robinson - first_name: Maria Carmela full_name: Roccheri, Maria Carmela last_name: Roccheri - first_name: Stephane full_name: Rocchi, Stephane last_name: Rocchi - first_name: George G. full_name: Rodney, George G. last_name: Rodney - first_name: Tiago full_name: Rodrigues, Tiago last_name: Rodrigues - first_name: Vagner Ramon full_name: Rodrigues Silva, Vagner Ramon last_name: Rodrigues Silva - first_name: Amaia full_name: Rodriguez, Amaia last_name: Rodriguez - first_name: Ruth full_name: Rodriguez-Barrueco, Ruth last_name: Rodriguez-Barrueco - first_name: Nieves full_name: Rodriguez-Henche, Nieves last_name: Rodriguez-Henche - first_name: Humberto full_name: Rodriguez-Rocha, Humberto last_name: Rodriguez-Rocha - first_name: Jeroen full_name: Roelofs, Jeroen last_name: Roelofs - first_name: Robert S. full_name: Rogers, Robert S. last_name: Rogers - first_name: Vladimir V. full_name: Rogov, Vladimir V. last_name: Rogov - first_name: Ana I. full_name: Rojo, Ana I. last_name: Rojo - first_name: Krzysztof full_name: Rolka, Krzysztof last_name: Rolka - first_name: Vanina full_name: Romanello, Vanina last_name: Romanello - first_name: Luigina full_name: Romani, Luigina last_name: Romani - first_name: Alessandra full_name: Romano, Alessandra last_name: Romano - first_name: Patricia S. full_name: Romano, Patricia S. last_name: Romano - first_name: David full_name: Romeo-Guitart, David last_name: Romeo-Guitart - first_name: Luis C. full_name: Romero, Luis C. last_name: Romero - first_name: Montserrat full_name: Romero, Montserrat last_name: Romero - first_name: Joseph C. full_name: Roney, Joseph C. last_name: Roney - first_name: Christopher full_name: Rongo, Christopher last_name: Rongo - first_name: Sante full_name: Roperto, Sante last_name: Roperto - first_name: Mathias T. full_name: Rosenfeldt, Mathias T. last_name: Rosenfeldt - first_name: Philip full_name: Rosenstiel, Philip last_name: Rosenstiel - first_name: Anne G. full_name: Rosenwald, Anne G. last_name: Rosenwald - first_name: Kevin A. full_name: Roth, Kevin A. last_name: Roth - first_name: Lynn full_name: Roth, Lynn last_name: Roth - first_name: Steven full_name: Roth, Steven last_name: Roth - first_name: Kasper M.A. full_name: Rouschop, Kasper M.A. last_name: Rouschop - first_name: Benoit D. full_name: Roussel, Benoit D. last_name: Roussel - first_name: Sophie full_name: Roux, Sophie last_name: Roux - first_name: Patrizia full_name: Rovere-Querini, Patrizia last_name: Rovere-Querini - first_name: Ajit full_name: Roy, Ajit last_name: Roy - first_name: Aurore full_name: Rozieres, Aurore last_name: Rozieres - first_name: Diego full_name: Ruano, Diego last_name: Ruano - first_name: David C. full_name: Rubinsztein, David C. last_name: Rubinsztein - first_name: Maria P. full_name: Rubtsova, Maria P. last_name: Rubtsova - first_name: Klaus full_name: Ruckdeschel, Klaus last_name: Ruckdeschel - first_name: Christoph full_name: Ruckenstuhl, Christoph last_name: Ruckenstuhl - first_name: Emil full_name: Rudolf, Emil last_name: Rudolf - first_name: Rüdiger full_name: Rudolf, Rüdiger last_name: Rudolf - first_name: Alessandra full_name: Ruggieri, Alessandra last_name: Ruggieri - first_name: Avnika Ashok full_name: Ruparelia, Avnika Ashok last_name: Ruparelia - first_name: Paola full_name: Rusmini, Paola last_name: Rusmini - first_name: Ryan R. full_name: Russell, Ryan R. last_name: Russell - first_name: Gian Luigi full_name: Russo, Gian Luigi last_name: Russo - first_name: Maria full_name: Russo, Maria last_name: Russo - first_name: Rossella full_name: Russo, Rossella last_name: Russo - first_name: Oxana O. full_name: Ryabaya, Oxana O. last_name: Ryabaya - first_name: Kevin M. full_name: Ryan, Kevin M. last_name: Ryan - first_name: Kwon Yul full_name: Ryu, Kwon Yul last_name: Ryu - first_name: Maria full_name: Sabater-Arcis, Maria last_name: Sabater-Arcis - first_name: Ulka full_name: Sachdev, Ulka last_name: Sachdev - first_name: Michael full_name: Sacher, Michael last_name: Sacher - first_name: Carsten full_name: Sachse, Carsten last_name: Sachse - first_name: Abhishek full_name: Sadhu, Abhishek last_name: Sadhu - first_name: Junichi full_name: Sadoshima, Junichi last_name: Sadoshima - first_name: Nathaniel full_name: Safren, Nathaniel last_name: Safren - first_name: Paul full_name: Saftig, Paul last_name: Saftig - first_name: Antonia P. full_name: Sagona, Antonia P. last_name: Sagona - first_name: Gaurav full_name: Sahay, Gaurav last_name: Sahay - first_name: Amirhossein full_name: Sahebkar, Amirhossein last_name: Sahebkar - first_name: Mustafa full_name: Sahin, Mustafa last_name: Sahin - first_name: Ozgur full_name: Sahin, Ozgur last_name: Sahin - first_name: Sumit full_name: Sahni, Sumit last_name: Sahni - first_name: Nayuta full_name: Saito, Nayuta last_name: Saito - first_name: Shigeru full_name: Saito, Shigeru last_name: Saito - first_name: Tsunenori full_name: Saito, Tsunenori last_name: Saito - first_name: Ryohei full_name: Sakai, Ryohei last_name: Sakai - first_name: Yasuyoshi full_name: Sakai, Yasuyoshi last_name: Sakai - first_name: Jun Ichi full_name: Sakamaki, Jun Ichi last_name: Sakamaki - first_name: Kalle full_name: Saksela, Kalle last_name: Saksela - first_name: Gloria full_name: Salazar, Gloria last_name: Salazar - first_name: Anna full_name: Salazar-Degracia, Anna last_name: Salazar-Degracia - first_name: Ghasem H. full_name: Salekdeh, Ghasem H. last_name: Salekdeh - first_name: Ashok K. full_name: Saluja, Ashok K. last_name: Saluja - first_name: Belém full_name: Sampaio-Marques, Belém last_name: Sampaio-Marques - first_name: Maria Cecilia full_name: Sanchez, Maria Cecilia last_name: Sanchez - first_name: Jose A. full_name: Sanchez-Alcazar, Jose A. last_name: Sanchez-Alcazar - first_name: Victoria full_name: Sanchez-Vera, Victoria last_name: Sanchez-Vera - first_name: Vanessa full_name: Sancho-Shimizu, Vanessa last_name: Sancho-Shimizu - first_name: J. Thomas full_name: Sanderson, J. Thomas last_name: Sanderson - first_name: Marco full_name: Sandri, Marco last_name: Sandri - first_name: Stefano full_name: Santaguida, Stefano last_name: Santaguida - first_name: Laura full_name: Santambrogio, Laura last_name: Santambrogio - first_name: Magda M. full_name: Santana, Magda M. last_name: Santana - first_name: Giorgio full_name: Santoni, Giorgio last_name: Santoni - first_name: Alberto full_name: Sanz, Alberto last_name: Sanz - first_name: Pascual full_name: Sanz, Pascual last_name: Sanz - first_name: Shweta full_name: Saran, Shweta last_name: Saran - first_name: Marco full_name: Sardiello, Marco last_name: Sardiello - first_name: Timothy J. full_name: Sargeant, Timothy J. last_name: Sargeant - first_name: Apurva full_name: Sarin, Apurva last_name: Sarin - first_name: Chinmoy full_name: Sarkar, Chinmoy last_name: Sarkar - first_name: Sovan full_name: Sarkar, Sovan last_name: Sarkar - first_name: Maria Rosa full_name: Sarrias, Maria Rosa last_name: Sarrias - first_name: Surajit full_name: Sarkar, Surajit last_name: Sarkar - first_name: Dipanka Tanu full_name: Sarmah, Dipanka Tanu last_name: Sarmah - first_name: Jaakko full_name: Sarparanta, Jaakko last_name: Sarparanta - first_name: Aishwarya full_name: Sathyanarayan, Aishwarya last_name: Sathyanarayan - first_name: Ranganayaki full_name: Sathyanarayanan, Ranganayaki last_name: Sathyanarayanan - first_name: K. Matthew full_name: Scaglione, K. 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Ivana full_name: Scovassi, A. 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first_name: Elena full_name: Seranova, Elena last_name: Seranova - first_name: Consolato full_name: Sergi, Consolato last_name: Sergi - first_name: Ruth full_name: Serra-Moreno, Ruth last_name: Serra-Moreno - first_name: Hiromi full_name: Sesaki, Hiromi last_name: Sesaki - first_name: Carmine full_name: Settembre, Carmine last_name: Settembre - first_name: Subba Rao Gangi full_name: Setty, Subba Rao Gangi last_name: Setty - first_name: Gianluca full_name: Sgarbi, Gianluca last_name: Sgarbi - first_name: Ou full_name: Sha, Ou last_name: Sha - first_name: John J. full_name: Shacka, John J. last_name: Shacka - first_name: Javeed A. full_name: Shah, Javeed A. last_name: Shah - first_name: Dantong full_name: Shang, Dantong last_name: Shang - first_name: Changshun full_name: Shao, Changshun last_name: Shao - first_name: Feng full_name: Shao, Feng last_name: Shao - first_name: Soroush full_name: Sharbati, Soroush last_name: Sharbati - first_name: Lisa M. full_name: Sharkey, Lisa M. last_name: Sharkey - first_name: Dipali full_name: Sharma, Dipali last_name: Sharma - first_name: Gaurav full_name: Sharma, Gaurav last_name: Sharma - first_name: Kulbhushan full_name: Sharma, Kulbhushan last_name: Sharma - first_name: Pawan full_name: Sharma, Pawan last_name: Sharma - first_name: Surendra full_name: Sharma, Surendra last_name: Sharma - first_name: Han Ming full_name: Shen, Han Ming last_name: Shen - first_name: Hongtao full_name: Shen, Hongtao last_name: Shen - first_name: Jiangang full_name: Shen, Jiangang last_name: Shen - first_name: Ming full_name: Shen, Ming last_name: Shen - first_name: Weili full_name: Shen, Weili last_name: Shen - first_name: Zheni full_name: Shen, Zheni last_name: Shen - first_name: Rui full_name: Sheng, Rui last_name: Sheng - first_name: Zhi full_name: Sheng, Zhi last_name: Sheng - first_name: Zu Hang full_name: Sheng, Zu Hang last_name: Sheng - first_name: Jianjian full_name: Shi, Jianjian last_name: Shi - first_name: Xiaobing full_name: Shi, Xiaobing last_name: Shi - first_name: Ying Hong full_name: Shi, Ying Hong last_name: Shi - first_name: Kahori full_name: Shiba-Fukushima, Kahori last_name: Shiba-Fukushima - first_name: Jeng Jer full_name: Shieh, Jeng Jer last_name: Shieh - first_name: Yohta full_name: Shimada, Yohta last_name: Shimada - first_name: Shigeomi full_name: Shimizu, Shigeomi last_name: Shimizu - first_name: Makoto full_name: Shimozawa, Makoto last_name: Shimozawa - first_name: Takahiro full_name: Shintani, Takahiro last_name: Shintani - first_name: Christopher J. full_name: Shoemaker, Christopher J. last_name: Shoemaker - first_name: Shahla full_name: Shojaei, Shahla last_name: Shojaei - first_name: Ikuo full_name: Shoji, Ikuo last_name: Shoji - first_name: Bhupendra V. full_name: Shravage, Bhupendra V. last_name: Shravage - first_name: Viji full_name: Shridhar, Viji last_name: Shridhar - first_name: Chih Wen full_name: Shu, Chih Wen last_name: Shu - first_name: Hong Bing full_name: Shu, Hong Bing last_name: Shu - first_name: Ke full_name: Shui, Ke last_name: Shui - first_name: Arvind K. full_name: Shukla, Arvind K. last_name: Shukla - first_name: Timothy E. full_name: Shutt, Timothy E. last_name: Shutt - first_name: Valentina full_name: Sica, Valentina last_name: Sica - first_name: Aleem full_name: Siddiqui, Aleem last_name: Siddiqui - first_name: Amanda full_name: Sierra, Amanda last_name: Sierra - first_name: Virginia full_name: Sierra-Torre, Virginia last_name: Sierra-Torre - first_name: Santiago full_name: Signorelli, Santiago last_name: Signorelli - first_name: Payel full_name: Sil, Payel last_name: Sil - first_name: Bruno J.De Andrade full_name: Silva, Bruno J.De Andrade last_name: Silva - first_name: Johnatas D. full_name: Silva, Johnatas D. last_name: Silva - first_name: Eduardo full_name: Silva-Pavez, Eduardo last_name: Silva-Pavez - first_name: Sandrine full_name: Silvente-Poirot, Sandrine last_name: Silvente-Poirot - first_name: Rachel E. full_name: Simmonds, Rachel E. last_name: Simmonds - first_name: Anna Katharina full_name: Simon, Anna Katharina last_name: Simon - first_name: Hans Uwe full_name: Simon, Hans Uwe last_name: Simon - first_name: Matias full_name: Simons, Matias last_name: Simons - first_name: Anurag full_name: Singh, Anurag last_name: Singh - first_name: Lalit P. full_name: Singh, Lalit P. last_name: Singh - first_name: Rajat full_name: Singh, Rajat last_name: Singh - first_name: Shivendra V. full_name: Singh, Shivendra V. last_name: Singh - first_name: Shrawan K. full_name: Singh, Shrawan K. last_name: Singh - first_name: Sudha B. full_name: Singh, Sudha B. last_name: Singh - first_name: Sunaina full_name: Singh, Sunaina last_name: Singh - first_name: Surinder Pal full_name: Singh, Surinder Pal last_name: Singh - first_name: Debasish full_name: Sinha, Debasish last_name: Sinha - first_name: Rohit Anthony full_name: Sinha, Rohit Anthony last_name: Sinha - first_name: Sangita full_name: Sinha, Sangita last_name: Sinha - first_name: Agnieszka full_name: Sirko, Agnieszka last_name: Sirko - first_name: Kapil full_name: Sirohi, Kapil last_name: Sirohi - first_name: Efthimios L. full_name: Sivridis, Efthimios L. last_name: Sivridis - first_name: Panagiotis full_name: Skendros, Panagiotis last_name: Skendros - first_name: Aleksandra full_name: Skirycz, Aleksandra last_name: Skirycz - first_name: Iva full_name: Slaninová, Iva last_name: Slaninová - first_name: Soraya S. full_name: Smaili, Soraya S. last_name: Smaili - first_name: Andrei full_name: Smertenko, Andrei last_name: Smertenko - first_name: Matthew D. full_name: Smith, Matthew D. last_name: Smith - first_name: Stefaan J. full_name: Soenen, Stefaan J. last_name: Soenen - first_name: Eun Jung full_name: Sohn, Eun Jung last_name: Sohn - first_name: Sophia P.M. full_name: Sok, Sophia P.M. last_name: Sok - first_name: Giancarlo full_name: Solaini, Giancarlo last_name: Solaini - first_name: Thierry full_name: Soldati, Thierry last_name: Soldati - first_name: Scott A. full_name: Soleimanpour, Scott A. last_name: Soleimanpour - first_name: Rosa M. full_name: Soler, Rosa M. last_name: Soler - first_name: Alexei full_name: Solovchenko, Alexei last_name: Solovchenko - first_name: Jason A. full_name: Somarelli, Jason A. last_name: Somarelli - first_name: Avinash full_name: Sonawane, Avinash last_name: Sonawane - first_name: Fuyong full_name: Song, Fuyong last_name: Song - first_name: Hyun Kyu full_name: Song, Hyun Kyu last_name: Song - first_name: Ju Xian full_name: Song, Ju Xian last_name: Song - first_name: Kunhua full_name: Song, Kunhua last_name: Song - first_name: Zhiyin full_name: Song, Zhiyin last_name: Song - first_name: Leandro R. full_name: Soria, Leandro R. last_name: Soria - first_name: Maurizio full_name: Sorice, Maurizio last_name: Sorice - first_name: Alexander A. full_name: Soukas, Alexander A. last_name: Soukas - first_name: Sandra Fausia full_name: Soukup, Sandra Fausia last_name: Soukup - first_name: Diana full_name: Sousa, Diana last_name: Sousa - first_name: Nadia full_name: Sousa, Nadia last_name: Sousa - first_name: Paul A. full_name: Spagnuolo, Paul A. last_name: Spagnuolo - 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Van Kaer, J. Van Loosdregt, S.J.L. Van Wijk, W. Vandenberghe, I. Vanhorebeek, M.A. Vannier-Santos, N. Vannini, M.C. Vanrell, C. Vantaggiato, G. Varano, I. Varela-Nieto, M. Varga, M.H. Vasconcelos, S. Vats, D.G. Vavvas, I. Vega-Naredo, S. Vega-Rubin-De-Celis, G. Velasco, A.P. Velázquez, T. Vellai, E. Vellenga, F. Velotti, M. Verdier, P. Verginis, I. Vergne, P. Verkade, M. Verma, P. Verstreken, T. Vervliet, J. Vervoorts, A.T. Vessoni, V.M. Victor, M. Vidal, C. Vidoni, O.V. Vieira, R.D. Vierstra, S. Viganó, H. Vihinen, V. Vijayan, M. Vila, M. Vilar, J.M. Villalba, A. Villalobo, B. Villarejo-Zori, F. Villarroya, J. Villarroya, O. Vincent, C. Vindis, C. Viret, M.T. Viscomi, D. Visnjic, I. Vitale, D.J. Vocadlo, O.V. Voitsekhovskaja, C. Volonté, M. Volta, M. Vomero, C. Von Haefen, M.A. Vooijs, W. Voos, L. Vucicevic, R. Wade-Martins, S. Waguri, K.A. Waite, S. Wakatsuki, D.W. Walker, M.J. Walker, S.A. Walker, J. Walter, F.G. Wandosell, B. Wang, C.Y. Wang, C. Wang, C. Wang, C. Wang, C.Y. 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Tong, Autophagy 17 (2021) 1–382. date_created: 2021-03-28T22:01:44Z date_published: 2021-02-08T00:00:00Z date_updated: 2023-10-16T09:43:56Z day: '08' department: - _id: JiFr - _id: CaHe doi: 10.1080/15548627.2020.1797280 external_id: isi: - '000636121800001' pmid: - '33634751' intvolume: ' 17' isi: 1 issue: '1' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1080/15548627.2020.1797280 month: '02' oa: 1 oa_version: Published Version page: 1-382 pmid: 1 publication: Autophagy publication_identifier: eissn: - 1554-8635 issn: - 1554-8627 publication_status: published publisher: Taylor & Francis quality_controlled: '1' scopus_import: '1' status: public title: Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 17 year: '2021' ... --- _id: '10223' abstract: - lang: eng text: Growth regulation tailors development in plants to their environment. A prominent example of this is the response to gravity, in which shoots bend up and roots bend down1. This paradox is based on opposite effects of the phytohormone auxin, which promotes cell expansion in shoots while inhibiting it in roots via a yet unknown cellular mechanism2. Here, by combining microfluidics, live imaging, genetic engineering and phosphoproteomics in Arabidopsis thaliana, we advance understanding of how auxin inhibits root growth. We show that auxin activates two distinct, antagonistically acting signalling pathways that converge on rapid regulation of apoplastic pH, a causative determinant of growth. Cell surface-based TRANSMEMBRANE KINASE1 (TMK1) interacts with and mediates phosphorylation and activation of plasma membrane H+-ATPases for apoplast acidification, while intracellular canonical auxin signalling promotes net cellular H+ influx, causing apoplast alkalinization. Simultaneous activation of these two counteracting mechanisms poises roots for rapid, fine-tuned growth modulation in navigating complex soil environments. acknowledged_ssus: - _id: LifeSc - _id: M-Shop - _id: Bio acknowledgement: We thank N. Gnyliukh and L. Hörmayer for technical assistance and N. Paris for sharing PM-Cyto seeds. We gratefully acknowledge the Life Science, Machine Shop and Bioimaging Facilities of IST Austria. This project has received funding from the European Research Council Advanced Grant (ETAP-742985) and the Austrian Science Fund (FWF) under I 3630-B25 to J.F., the National Institutes of Health (GM067203) to W.M.G., the Netherlands Organization for Scientific Research (NWO; VIDI-864.13.001), Research Foundation-Flanders (FWO; Odysseus II G0D0515N) and a European Research Council Starting Grant (TORPEDO-714055) to W.S. and B.D.R., the VICI grant (865.14.001) from the Netherlands Organization for Scientific Research to M.R. and D.W., the Australian Research Council and China National Distinguished Expert Project (WQ20174400441) to S.S., the MEXT/JSPS KAKENHI to K.T. (20K06685) and T.K. (20H05687 and 20H05910), the European Union’s Horizon 2020 research and innovation programme under Marie Skłodowska-Curie grant agreement no. 665385 and the DOC Fellowship of the Austrian Academy of Sciences to L.L., and the China Scholarship Council to J.C. article_processing_charge: No article_type: original author: - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Mark full_name: Roosjen, Mark last_name: Roosjen - first_name: Koji full_name: Takahashi, Koji last_name: Takahashi - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Jack full_name: Merrin, Jack id: 4515C308-F248-11E8-B48F-1D18A9856A87 last_name: Merrin orcid: 0000-0001-5145-4609 - first_name: Jian full_name: Chen, Jian last_name: Chen - first_name: Lana full_name: Shabala, Lana last_name: Shabala - first_name: Wouter full_name: Smet, Wouter last_name: Smet - first_name: Hong full_name: Ren, Hong last_name: Ren - first_name: Steffen full_name: Vanneste, Steffen last_name: Vanneste - first_name: Sergey full_name: Shabala, Sergey last_name: Shabala - first_name: Bert full_name: De Rybel, Bert last_name: De Rybel - first_name: Dolf full_name: Weijers, Dolf last_name: Weijers - first_name: Toshinori full_name: Kinoshita, Toshinori last_name: Kinoshita - first_name: William M. full_name: Gray, William M. last_name: Gray - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Li L, Verstraeten I, Roosjen M, et al. Cell surface and intracellular auxin signalling for H+ fluxes in root growth. Nature. 2021;599(7884):273-277. doi:10.1038/s41586-021-04037-6 apa: Li, L., Verstraeten, I., Roosjen, M., Takahashi, K., Rodriguez Solovey, L., Merrin, J., … Friml, J. (2021). Cell surface and intracellular auxin signalling for H+ fluxes in root growth. Nature. Springer Nature. https://doi.org/10.1038/s41586-021-04037-6 chicago: Li, Lanxin, Inge Verstraeten, Mark Roosjen, Koji Takahashi, Lesia Rodriguez Solovey, Jack Merrin, Jian Chen, et al. “Cell Surface and Intracellular Auxin Signalling for H+ Fluxes in Root Growth.” Nature. Springer Nature, 2021. https://doi.org/10.1038/s41586-021-04037-6. ieee: L. Li et al., “Cell surface and intracellular auxin signalling for H+ fluxes in root growth,” Nature, vol. 599, no. 7884. Springer Nature, pp. 273–277, 2021. ista: Li L, Verstraeten I, Roosjen M, Takahashi K, Rodriguez Solovey L, Merrin J, Chen J, Shabala L, Smet W, Ren H, Vanneste S, Shabala S, De Rybel B, Weijers D, Kinoshita T, Gray WM, Friml J. 2021. Cell surface and intracellular auxin signalling for H+ fluxes in root growth. Nature. 599(7884), 273–277. mla: Li, Lanxin, et al. “Cell Surface and Intracellular Auxin Signalling for H+ Fluxes in Root Growth.” Nature, vol. 599, no. 7884, Springer Nature, 2021, pp. 273–77, doi:10.1038/s41586-021-04037-6. short: L. Li, I. Verstraeten, M. Roosjen, K. Takahashi, L. Rodriguez Solovey, J. Merrin, J. Chen, L. Shabala, W. Smet, H. Ren, S. Vanneste, S. Shabala, B. De Rybel, D. Weijers, T. Kinoshita, W.M. Gray, J. Friml, Nature 599 (2021) 273–277. date_created: 2021-11-07T23:01:25Z date_published: 2021-11-11T00:00:00Z date_updated: 2023-10-18T08:30:53Z day: '11' department: - _id: JiFr - _id: NanoFab doi: 10.1038/s41586-021-04037-6 ec_funded: 1 external_id: isi: - '000713338100006' pmid: - '34707283' intvolume: ' 599' isi: 1 issue: '7884' keyword: - Multidisciplinary language: - iso: eng main_file_link: - open_access: '1' url: https://www.doi.org/10.21203/rs.3.rs-266395/v3 month: '11' oa: 1 oa_version: Preprint page: 273-277 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program - _id: 26B4D67E-B435-11E9-9278-68D0E5697425 grant_number: '25351' name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated Rapid Growth Inhibition in Arabidopsis Root' publication: Nature publication_identifier: eissn: - '14764687' issn: - '00280836' publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: link: - description: News on IST Webpage relation: press_release url: https://ist.ac.at/en/news/stop-and-grow/ record: - id: '10095' relation: earlier_version status: public scopus_import: '1' status: public title: Cell surface and intracellular auxin signalling for H+ fluxes in root growth type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 599 year: '2021' ... --- _id: '9189' abstract: - lang: eng text: Transposable elements exist widely throughout plant genomes and play important roles in plant evolution. Auxin is an important regulator that is traditionally associated with root development and drought stress adaptation. The DEEPER ROOTING 1 (DRO1) gene is a key component of rice drought avoidance. Here, we identified a transposon that acts as an autonomous auxin‐responsive promoter and its presence at specific genome positions conveys physiological adaptations related to drought avoidance. Rice varieties with high and auxin‐mediated transcription of DRO1 in the root tip show deeper and longer root phenotypes and are thus better adapted to drought. The INDITTO2 transposon contains an auxin response element and displays auxin‐responsive promoter activity; it is thus able to convey auxin regulation of transcription to genes in its proximity. In the rice Acuce, which displays DRO1‐mediated drought adaptation, the INDITTO2 transposon was found to be inserted at the promoter region of the DRO1 locus. Transgenesis‐based insertion of the INDITTO2 transposon into the DRO1 promoter of the non‐adapted rice variety Nipponbare was sufficient to promote its drought avoidance. Our data identify an example of how transposons can act as promoters and convey hormonal regulation to nearby loci, improving plant fitness in response to different abiotic stresses. article_processing_charge: No article_type: original author: - first_name: Y full_name: Zhao, Y last_name: Zhao - first_name: L full_name: Wu, L last_name: Wu - first_name: Q full_name: Fu, Q last_name: Fu - first_name: D full_name: Wang, D last_name: Wang - first_name: J full_name: Li, J last_name: Li - first_name: B full_name: Yao, B last_name: Yao - first_name: S full_name: Yu, S last_name: Yu - first_name: L full_name: Jiang, L last_name: Jiang - first_name: J full_name: Qian, J last_name: Qian - first_name: X full_name: Zhou, X last_name: Zhou - first_name: L full_name: Han, L last_name: Han - first_name: S full_name: Zhao, S last_name: Zhao - first_name: C full_name: Ma, C last_name: Ma - first_name: Y full_name: Zhang, Y last_name: Zhang - first_name: C full_name: Luo, C last_name: Luo - first_name: Q full_name: Dong, Q last_name: Dong - first_name: S full_name: Li, S last_name: Li - first_name: L full_name: Zhang, L last_name: Zhang - first_name: X full_name: Jiang, X last_name: Jiang - first_name: Y full_name: Li, Y last_name: Li - first_name: H full_name: Luo, H last_name: Luo - first_name: K full_name: Li, K last_name: Li - first_name: J full_name: Yang, J last_name: Yang - first_name: Q full_name: Luo, Q last_name: Luo - first_name: L full_name: Li, L last_name: Li - first_name: S full_name: Peng, S last_name: Peng - first_name: H full_name: Huang, H last_name: Huang - first_name: Z full_name: Zuo, Z last_name: Zuo - first_name: C full_name: Liu, C last_name: Liu - first_name: L full_name: Wang, L last_name: Wang - first_name: C full_name: Li, C last_name: Li - first_name: X full_name: He, X last_name: He - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Y full_name: Du, Y last_name: Du citation: ama: Zhao Y, Wu L, Fu Q, et al. INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance. Plant, Cell & Environment. 2021;44(6):1846-1857. doi:10.1111/pce.14029 apa: Zhao, Y., Wu, L., Fu, Q., Wang, D., Li, J., Yao, B., … Du, Y. (2021). INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance. Plant, Cell & Environment. Wiley. https://doi.org/10.1111/pce.14029 chicago: Zhao, Y, L Wu, Q Fu, D Wang, J Li, B Yao, S Yu, et al. “INDITTO2 Transposon Conveys Auxin-Mediated DRO1 Transcription for Rice Drought Avoidance.” Plant, Cell & Environment. Wiley, 2021. https://doi.org/10.1111/pce.14029. ieee: Y. Zhao et al., “INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance,” Plant, Cell & Environment, vol. 44, no. 6. Wiley, pp. 1846–1857, 2021. ista: Zhao Y, Wu L, Fu Q, Wang D, Li J, Yao B, Yu S, Jiang L, Qian J, Zhou X, Han L, Zhao S, Ma C, Zhang Y, Luo C, Dong Q, Li S, Zhang L, Jiang X, Li Y, Luo H, Li K, Yang J, Luo Q, Li L, Peng S, Huang H, Zuo Z, Liu C, Wang L, Li C, He X, Friml J, Du Y. 2021. INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance. Plant, Cell & Environment. 44(6), 1846–1857. mla: Zhao, Y., et al. “INDITTO2 Transposon Conveys Auxin-Mediated DRO1 Transcription for Rice Drought Avoidance.” Plant, Cell & Environment, vol. 44, no. 6, Wiley, 2021, pp. 1846–57, doi:10.1111/pce.14029. short: Y. Zhao, L. Wu, Q. Fu, D. Wang, J. Li, B. Yao, S. Yu, L. Jiang, J. Qian, X. Zhou, L. Han, S. Zhao, C. Ma, Y. Zhang, C. Luo, Q. Dong, S. Li, L. Zhang, X. Jiang, Y. Li, H. Luo, K. Li, J. Yang, Q. Luo, L. Li, S. Peng, H. Huang, Z. Zuo, C. Liu, L. Wang, C. Li, X. He, J. Friml, Y. Du, Plant, Cell & Environment 44 (2021) 1846–1857. date_created: 2021-02-24T10:07:21Z date_published: 2021-06-01T00:00:00Z date_updated: 2023-11-07T08:18:36Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/pce.14029 external_id: isi: - '000625398600001' pmid: - '33576018' file: - access_level: open_access checksum: a812418fede076741c9c4dc07f317068 content_type: application/pdf creator: amally date_created: 2023-11-02T17:02:11Z date_updated: 2023-11-02T17:02:11Z file_id: '14481' file_name: Zhao PlantCellEnv 2021_accepted.pdf file_size: 8437528 relation: main_file success: 1 file_date_updated: 2023-11-02T17:02:11Z has_accepted_license: '1' intvolume: ' 44' isi: 1 issue: '6' language: - iso: eng month: '06' oa: 1 oa_version: Submitted Version page: 1846-1857 pmid: 1 publication: Plant, Cell & Environment publication_identifier: eissn: - 1365-3040 issn: - 0140-7791 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 44 year: '2021' ... --- _id: '9887' abstract: - lang: eng text: Clathrin-mediated endocytosis is the major route of entry of cargos into cells and thus underpins many physiological processes. During endocytosis, an area of flat membrane is remodeled by proteins to create a spherical vesicle against intracellular forces. The protein machinery which mediates this membrane bending in plants is unknown. However, it is known that plant endocytosis is actin independent, thus indicating that plants utilize a unique mechanism to mediate membrane bending against high-turgor pressure compared to other model systems. Here, we investigate the TPLATE complex, a plant-specific endocytosis protein complex. It has been thought to function as a classical adaptor functioning underneath the clathrin coat. However, by using biochemical and advanced live microscopy approaches, we found that TPLATE is peripherally associated with clathrin-coated vesicles and localizes at the rim of endocytosis events. As this localization is more fitting to the protein machinery involved in membrane bending during endocytosis, we examined cells in which the TPLATE complex was disrupted and found that the clathrin structures present as flat patches. This suggests a requirement of the TPLATE complex for membrane bending during plant clathrin–mediated endocytosis. Next, we used in vitro biophysical assays to confirm that the TPLATE complex possesses protein domains with intrinsic membrane remodeling activity. These results redefine the role of the TPLATE complex and implicate it as a key component of the evolutionarily distinct plant endocytosis mechanism, which mediates endocytic membrane bending against the high-turgor pressure in plant cells. acknowledged_ssus: - _id: EM-Fac - _id: LifeSc - _id: Bio acknowledgement: 'We gratefully thank Julie Neveu and Dr. Amanda Barranco of the Grégory Vert laboratory for help preparing plants in France, Dr. Zuzana Gelova for help and advice with protoplast generation, Dr. Stéphane Vassilopoulos and Dr. Florian Schur for advice regarding EM tomography, Alejandro Marquiegui Alvaro for help with material generation, and Dr. Lukasz Kowalski for generously gifting us the mWasabi protein. This research was supported by the Scientific Service Units of Institute of Science and Technology Austria (IST Austria) through resources provided by the Electron Microscopy Facility, Lab Support Facility (particularly Dorota Jaworska), and the Bioimaging Facility. We acknowledge the Advanced Microscopy Facility of the Vienna BioCenter Core Facilities for use of the 3D SIM. For the mass spectrometry analysis of proteins, we acknowledge the University of Natural Resources and Life Sciences (BOKU) Core Facility Mass Spectrometry. This work was supported by the following funds: A.J. is supported by funding from the Austrian Science Fund I3630B25 to J.F. P.M. and E.B. are supported by Agence Nationale de la Recherche ANR-11-EQPX-0029 Morphoscope2 and ANR-10-INBS-04 France BioImaging. S.Y.B. is supported by the NSF No. 1121998 and 1614915. J.W. and D.V.D. are supported by the European Research Council Grant 682436 (to D.V.D.), a China Scholarship Council Grant 201508440249 (to J.W.), and by a Ghent University Special Research Co-funding Grant ST01511051 (to J.W.).' article_number: e2113046118 article_processing_charge: No article_type: original author: - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Dana A full_name: Dahhan, Dana A last_name: Dahhan - first_name: Nataliia full_name: Gnyliukh, Nataliia id: 390C1120-F248-11E8-B48F-1D18A9856A87 last_name: Gnyliukh orcid: 0000-0002-2198-0509 - first_name: Walter full_name: Kaufmann, Walter id: 3F99E422-F248-11E8-B48F-1D18A9856A87 last_name: Kaufmann orcid: 0000-0001-9735-5315 - first_name: Vanessa full_name: Zheden, Vanessa id: 39C5A68A-F248-11E8-B48F-1D18A9856A87 last_name: Zheden orcid: 0000-0002-9438-4783 - first_name: Tommaso full_name: Costanzo, Tommaso id: D93824F4-D9BA-11E9-BB12-F207E6697425 last_name: Costanzo orcid: 0000-0001-9732-3815 - first_name: Pierre full_name: Mahou, Pierre last_name: Mahou - first_name: Mónika full_name: Hrtyan, Mónika id: 45A71A74-F248-11E8-B48F-1D18A9856A87 last_name: Hrtyan - first_name: Jie full_name: Wang, Jie last_name: Wang - first_name: Juan L full_name: Aguilera Servin, Juan L id: 2A67C376-F248-11E8-B48F-1D18A9856A87 last_name: Aguilera Servin orcid: 0000-0002-2862-8372 - first_name: Daniël full_name: van Damme, Daniël last_name: van Damme - first_name: Emmanuel full_name: Beaurepaire, Emmanuel last_name: Beaurepaire - first_name: Martin full_name: Loose, Martin id: 462D4284-F248-11E8-B48F-1D18A9856A87 last_name: Loose orcid: 0000-0001-7309-9724 - first_name: Sebastian Y full_name: Bednarek, Sebastian Y last_name: Bednarek - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Johnson AJ, Dahhan DA, Gnyliukh N, et al. The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis. Proceedings of the National Academy of Sciences. 2021;118(51). doi:10.1073/pnas.2113046118 apa: Johnson, A. J., Dahhan, D. A., Gnyliukh, N., Kaufmann, W., Zheden, V., Costanzo, T., … Friml, J. (2021). The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis. Proceedings of the National Academy of Sciences. National Academy of Sciences. https://doi.org/10.1073/pnas.2113046118 chicago: Johnson, Alexander J, Dana A Dahhan, Nataliia Gnyliukh, Walter Kaufmann, Vanessa Zheden, Tommaso Costanzo, Pierre Mahou, et al. “The TPLATE Complex Mediates Membrane Bending during Plant Clathrin-Mediated Endocytosis.” Proceedings of the National Academy of Sciences. National Academy of Sciences, 2021. https://doi.org/10.1073/pnas.2113046118. ieee: A. J. Johnson et al., “The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis,” Proceedings of the National Academy of Sciences, vol. 118, no. 51. National Academy of Sciences, 2021. ista: Johnson AJ, Dahhan DA, Gnyliukh N, Kaufmann W, Zheden V, Costanzo T, Mahou P, Hrtyan M, Wang J, Aguilera Servin JL, van Damme D, Beaurepaire E, Loose M, Bednarek SY, Friml J. 2021. The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis. Proceedings of the National Academy of Sciences. 118(51), e2113046118. mla: Johnson, Alexander J., et al. “The TPLATE Complex Mediates Membrane Bending during Plant Clathrin-Mediated Endocytosis.” Proceedings of the National Academy of Sciences, vol. 118, no. 51, e2113046118, National Academy of Sciences, 2021, doi:10.1073/pnas.2113046118. short: A.J. Johnson, D.A. Dahhan, N. Gnyliukh, W. Kaufmann, V. Zheden, T. Costanzo, P. Mahou, M. Hrtyan, J. Wang, J.L. Aguilera Servin, D. van Damme, E. Beaurepaire, M. Loose, S.Y. Bednarek, J. Friml, Proceedings of the National Academy of Sciences 118 (2021). date_created: 2021-08-11T14:11:43Z date_published: 2021-12-14T00:00:00Z date_updated: 2024-02-19T11:06:09Z day: '14' ddc: - '580' department: - _id: JiFr - _id: MaLo - _id: EvBe - _id: EM-Fac - _id: NanoFab doi: 10.1073/pnas.2113046118 external_id: isi: - '000736417600043' pmid: - '34907016' file: - access_level: open_access checksum: 8d01e72e22c4fb1584e72d8601947069 content_type: application/pdf creator: cchlebak date_created: 2021-12-15T08:59:40Z date_updated: 2021-12-15T08:59:40Z file_id: '10546' file_name: 2021_PNAS_Johnson.pdf file_size: 2757340 relation: main_file success: 1 file_date_updated: 2021-12-15T08:59:40Z has_accepted_license: '1' intvolume: ' 118' isi: 1 issue: '51' language: - iso: eng month: '12' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Proceedings of the National Academy of Sciences publication_identifier: eissn: - 1091-6490 publication_status: published publisher: National Academy of Sciences quality_controlled: '1' related_material: link: - relation: earlier_version url: https://doi.org/10.1101/2021.04.26.441441 record: - id: '14510' relation: dissertation_contains status: public - id: '14988' relation: research_data status: public status: public title: The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 118 year: '2021' ... --- _id: '14988' abstract: - lang: eng text: Raw data generated from the publication - The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis by Johnson et al., 2021 In PNAS article_processing_charge: No author: - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 citation: ama: Johnson AJ. Raw data from Johnson et al, PNAS, 2021. 2021. doi:10.5281/ZENODO.5747100 apa: Johnson, A. J. (2021). Raw data from Johnson et al, PNAS, 2021. Zenodo. https://doi.org/10.5281/ZENODO.5747100 chicago: Johnson, Alexander J. “Raw Data from Johnson et Al, PNAS, 2021.” Zenodo, 2021. https://doi.org/10.5281/ZENODO.5747100. ieee: A. J. Johnson, “Raw data from Johnson et al, PNAS, 2021.” Zenodo, 2021. ista: Johnson AJ. 2021. Raw data from Johnson et al, PNAS, 2021, Zenodo, 10.5281/ZENODO.5747100. mla: Johnson, Alexander J. Raw Data from Johnson et Al, PNAS, 2021. Zenodo, 2021, doi:10.5281/ZENODO.5747100. short: A.J. Johnson, (2021). date_created: 2024-02-14T14:13:48Z date_published: 2021-12-01T00:00:00Z date_updated: 2024-02-19T11:06:09Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.5281/ZENODO.5747100 has_accepted_license: '1' main_file_link: - open_access: '1' url: https://doi.org/10.5281/zenodo.5747100 month: '12' oa: 1 oa_version: Published Version publisher: Zenodo related_material: record: - id: '9887' relation: used_in_publication status: public status: public title: Raw data from Johnson et al, PNAS, 2021 tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: research_data_reference user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 year: '2021' ... --- _id: '9992' abstract: - lang: eng text: "Blood – this is what animals use to heal wounds fast and efficient. Plants do not have blood circulation and their cells cannot move. However, plants have evolved remarkable capacities to regenerate tissues and organs preventing further damage. In my PhD research, I studied the wound healing in the Arabidopsis root. I used a UV laser to ablate single cells in the root tip and observed the consequent wound healing. Interestingly, the inner adjacent cells induced a\r\ndivision plane switch and subsequently adopted the cell type of the killed cell to replace it. We termed this form of wound healing “restorative divisions”. This initial observation triggered the questions of my PhD studies: How and why do cells orient their division planes, how do they feel the wound and why does this happen only in inner adjacent cells.\r\nFor answering these questions, I used a quite simple experimental setup: 5 day - old seedlings were stained with propidium iodide to visualize cell walls and dead cells; ablation was carried out using a special laser cutter and a confocal microscope. Adaptation of the novel vertical microscope system made it possible to observe wounds in real time. This revealed that restorative divisions occur at increased frequency compared to normal divisions. Additionally,\r\nthe major plant hormone auxin accumulates in wound adjacent cells and drives the expression of the wound-stress responsive transcription factor ERF115. Using this as a marker gene for wound responses, we found that an important part of wound signalling is the sensing of the collapse of the ablated cell. The collapse causes a radical pressure drop, which results in strong tissue deformations. These deformations manifest in an invasion of the now free spot specifically by the inner adjacent cells within seconds, probably because of higher pressure of the inner tissues. Long-term imaging revealed that those deformed cells continuously expand towards the wound hole and that this is crucial for the restorative division. These wound-expanding cells exhibit an abnormal, biphasic polarity of microtubule arrays\r\nbefore the division. Experiments inhibiting cell expansion suggest that it is the biphasic stretching that induces those MT arrays. Adapting the micromanipulator aspiration system from animal scientists at our institute confirmed the hypothesis that stretching influences microtubule stability. In conclusion, this shows that microtubules react to tissue deformation\r\nand this facilitates the observed division plane switch. This puts mechanical cues and tensions at the most prominent position for explaining the growth and wound healing properties of plants. Hence, it shines light onto the importance of understanding mechanical signal transduction. " acknowledged_ssus: - _id: Bio - _id: LifeSc alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 citation: ama: Hörmayer L. Wound healing in the Arabidopsis root meristem. 2021. doi:10.15479/at:ista:9992 apa: Hörmayer, L. (2021). Wound healing in the Arabidopsis root meristem. Institute of Science and Technology Austria. https://doi.org/10.15479/at:ista:9992 chicago: Hörmayer, Lukas. “Wound Healing in the Arabidopsis Root Meristem.” Institute of Science and Technology Austria, 2021. https://doi.org/10.15479/at:ista:9992. ieee: L. Hörmayer, “Wound healing in the Arabidopsis root meristem,” Institute of Science and Technology Austria, 2021. ista: Hörmayer L. 2021. Wound healing in the Arabidopsis root meristem. Institute of Science and Technology Austria. mla: Hörmayer, Lukas. Wound Healing in the Arabidopsis Root Meristem. Institute of Science and Technology Austria, 2021, doi:10.15479/at:ista:9992. short: L. Hörmayer, Wound Healing in the Arabidopsis Root Meristem, Institute of Science and Technology Austria, 2021. date_created: 2021-09-09T07:37:20Z date_published: 2021-09-13T00:00:00Z date_updated: 2023-09-07T13:38:33Z day: '13' ddc: - '575' degree_awarded: PhD department: - _id: GradSch - _id: JiFr doi: 10.15479/at:ista:9992 ec_funded: 1 file: - access_level: closed checksum: c763064adaa720e16066c1a4f9682bbb content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: lhoermaye date_created: 2021-09-09T07:29:48Z date_updated: 2021-09-15T22:30:26Z embargo_to: open_access file_id: '9993' file_name: Thesis_vupload.docx file_size: 25179004 relation: source_file - access_level: open_access checksum: 53911b06e93d7cdbbf4c7f4c162fa70f content_type: application/pdf creator: lhoermaye date_created: 2021-09-09T14:25:08Z date_updated: 2021-09-15T22:30:26Z embargo: 2021-09-09 file_id: '9996' file_name: Thesis_vfinal_pdfa.pdf file_size: 6246900 relation: main_file file_date_updated: 2021-09-15T22:30:26Z has_accepted_license: '1' language: - iso: eng month: '09' oa: 1 oa_version: Published Version page: '168' project: - _id: 262EF96E-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: P29988 name: RNA-directed DNA methylation in plant development - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication_identifier: issn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '6351' relation: part_of_dissertation status: public - id: '6943' relation: part_of_dissertation status: public - id: '8002' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: Wound healing in the Arabidopsis root meristem tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2021' ... --- _id: '9010' abstract: - lang: eng text: Availability of the essential macronutrient nitrogen in soil plays a critical role in plant growth, development, and impacts agricultural productivity. Plants have evolved different strategies for sensing and responding to heterogeneous nitrogen distribution. Modulation of root system architecture, including primary root growth and branching, is among the most essential plant adaptions to ensure adequate nitrogen acquisition. However, the immediate molecular pathways coordinating the adjustment of root growth in response to distinct nitrogen sources, such as nitrate or ammonium, are poorly understood. Here, we show that growth as manifested by cell division and elongation is synchronized by coordinated auxin flux between two adjacent outer tissue layers of the root. This coordination is achieved by nitrate‐dependent dephosphorylation of the PIN2 auxin efflux carrier at a previously uncharacterized phosphorylation site, leading to subsequent PIN2 lateralization and thereby regulating auxin flow between adjacent tissues. A dynamic computer model based on our experimental data successfully recapitulates experimental observations. Our study provides mechanistic insights broadening our understanding of root growth mechanisms in dynamic environments. acknowledged_ssus: - _id: Bio acknowledgement: 'We acknowledge Gergely Molnar for critical reading of the manuscript, Alexander Johnson for language editing and Yulija Salanenka for technical assistance. Work in the Benkova laboratory was supported by the Austrian Science Fund (FWF01_I1774S) to KO, RA and EB. Work in the Benkova laboratory was supported by the Austrian Science Fund (FWF01_I1774S) to KO, RA and EB and by the DOC Fellowship Programme of the AustrianAcademy of Sciences (25008) to C.A. Work in the Wabnik laboratory was supported by the Programa de Atraccion de Talento 2017 (Comunidad deMadrid, 2017-T1/BIO-5654 to K.W.), Severo Ochoa Programme for Centres of Excellence in R&D from the Agencia Estatal de Investigacion of Spain (grantSEV-2016-0672 (2017-2021) to K.W. via the CBGP) and Programa Estatal de Generacion del Conocimiento y Fortalecimiento Científico y Tecnologico del Sistema de I+D+I 2019 (PGC2018-093387-A-I00) from MICIU (to K.W.). M.M.was supported by a postdoctoral contract associated to SEV-2016-0672.We acknowledge the Bioimaging Facility in IST-Austria and the Advanced Microscopy Facility of the Vienna Bio Center Core Facilities, member of the Vienna Bio Center Austria, for use of the OMX v43D SIM microscope. AJ was supported by the Austrian Science Fund (FWF): I03630 to J.F' article_number: e106862 article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: Krisztina full_name: Ötvös, Krisztina id: 29B901B0-F248-11E8-B48F-1D18A9856A87 last_name: Ötvös orcid: 0000-0002-5503-4983 - first_name: Marco full_name: Marconi, Marco last_name: Marconi - first_name: Andrea full_name: Vega, Andrea last_name: Vega - first_name: Jose full_name: O’Brien, Jose last_name: O’Brien - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Rashed full_name: Abualia, Rashed id: 4827E134-F248-11E8-B48F-1D18A9856A87 last_name: Abualia orcid: 0000-0002-9357-9415 - first_name: Livio full_name: Antonielli, Livio last_name: Antonielli - first_name: Juan C full_name: Montesinos López, Juan C id: 310A8E3E-F248-11E8-B48F-1D18A9856A87 last_name: Montesinos López orcid: 0000-0001-9179-6099 - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Candela full_name: Cuesta, Candela id: 33A3C818-F248-11E8-B48F-1D18A9856A87 last_name: Cuesta orcid: 0000-0003-1923-2410 - first_name: Christina full_name: Artner, Christina id: 45DF286A-F248-11E8-B48F-1D18A9856A87 last_name: Artner - first_name: Eleonore full_name: Bouguyon, Eleonore last_name: Bouguyon - first_name: Alain full_name: Gojon, Alain last_name: Gojon - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Rodrigo A. full_name: Gutiérrez, Rodrigo A. last_name: Gutiérrez - first_name: Krzysztof T full_name: Wabnik, Krzysztof T id: 4DE369A4-F248-11E8-B48F-1D18A9856A87 last_name: Wabnik orcid: 0000-0001-7263-0560 - first_name: Eva full_name: Benková, Eva id: 38F4F166-F248-11E8-B48F-1D18A9856A87 last_name: Benková orcid: 0000-0002-8510-9739 citation: ama: Ötvös K, Marconi M, Vega A, et al. Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport. EMBO Journal. 2021;40(3). doi:10.15252/embj.2020106862 apa: Ötvös, K., Marconi, M., Vega, A., O’Brien, J., Johnson, A. J., Abualia, R., … Benková, E. (2021). Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport. EMBO Journal. Embo Press. https://doi.org/10.15252/embj.2020106862 chicago: Ötvös, Krisztina, Marco Marconi, Andrea Vega, Jose O’Brien, Alexander J Johnson, Rashed Abualia, Livio Antonielli, et al. “Modulation of Plant Root Growth by Nitrogen Source-Defined Regulation of Polar Auxin Transport.” EMBO Journal. Embo Press, 2021. https://doi.org/10.15252/embj.2020106862. ieee: K. Ötvös et al., “Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport,” EMBO Journal, vol. 40, no. 3. Embo Press, 2021. ista: Ötvös K, Marconi M, Vega A, O’Brien J, Johnson AJ, Abualia R, Antonielli L, Montesinos López JC, Zhang Y, Tan S, Cuesta C, Artner C, Bouguyon E, Gojon A, Friml J, Gutiérrez RA, Wabnik KT, Benková E. 2021. Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport. EMBO Journal. 40(3), e106862. mla: Ötvös, Krisztina, et al. “Modulation of Plant Root Growth by Nitrogen Source-Defined Regulation of Polar Auxin Transport.” EMBO Journal, vol. 40, no. 3, e106862, Embo Press, 2021, doi:10.15252/embj.2020106862. short: K. Ötvös, M. Marconi, A. Vega, J. O’Brien, A.J. Johnson, R. Abualia, L. Antonielli, J.C. Montesinos López, Y. Zhang, S. Tan, C. Cuesta, C. Artner, E. Bouguyon, A. Gojon, J. Friml, R.A. Gutiérrez, K.T. Wabnik, E. Benková, EMBO Journal 40 (2021). date_created: 2021-01-17T23:01:12Z date_published: 2021-02-01T00:00:00Z date_updated: 2024-03-27T23:30:39Z day: '01' ddc: - '580' department: - _id: JiFr - _id: EvBe doi: 10.15252/embj.2020106862 external_id: isi: - '000604645600001' pmid: - ' 33399250' file: - access_level: open_access checksum: dc55c900f3b061d6c2790b8813d759a3 content_type: application/pdf creator: dernst date_created: 2021-02-11T12:28:29Z date_updated: 2021-02-11T12:28:29Z file_id: '9110' file_name: 2021_Embo_Otvos.pdf file_size: 2358617 relation: main_file success: 1 file_date_updated: 2021-02-11T12:28:29Z has_accepted_license: '1' intvolume: ' 40' isi: 1 issue: '3' language: - iso: eng month: '02' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 2542D156-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I 1774-B16 name: Hormone cross-talk drives nutrient dependent plant development - _id: 2685A872-B435-11E9-9278-68D0E5697425 name: Hormonal regulation of plant adaptive responses to environmental signals - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: EMBO Journal publication_identifier: eissn: - '14602075' issn: - '02614189' publication_status: published publisher: Embo Press quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/a-plants-way-to-its-favorite-food/ record: - id: '10303' relation: dissertation_contains status: public scopus_import: '1' status: public title: Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 40 year: '2021' ... --- _id: '8931' abstract: - lang: eng text: "Auxin is a major plant growth regulator, but current models on auxin perception and signaling cannot explain the whole plethora of auxin effects, in particular those associated with rapid responses. A possible candidate for a component of additional auxin perception mechanisms is the AUXIN BINDING PROTEIN 1 (ABP1), whose function in planta remains unclear.\r\nHere we combined expression analysis with gain- and loss-of-function approaches to analyze the role of ABP1 in plant development. ABP1 shows a broad expression largely overlapping with, but not regulated by, transcriptional auxin response activity. Furthermore, ABP1 activity is not essential for the transcriptional auxin signaling. Genetic in planta analysis revealed that abp1 loss-of-function mutants show largely normal development with minor defects in bolting. On the other hand, ABP1 gain-of-function alleles show a broad range of growth and developmental defects, including root and hypocotyl growth and bending, lateral root and leaf development, bolting, as well as response to heat stress. At the cellular level, ABP1 gain-of-function leads to impaired auxin effect on PIN polar distribution and affects BFA-sensitive PIN intracellular aggregation.\r\nThe gain-of-function analysis suggests a broad, but still mechanistically unclear involvement of ABP1 in plant development, possibly masked in abp1 loss-of-function mutants by a functional redundancy." acknowledged_ssus: - _id: Bio - _id: LifeSc acknowledgement: We would like to acknowledge Bioimaging and Life Science Facilities at IST Austria for continuous support and also the Plant Sciences Core Facility of CEITEC Masaryk University for their support with obtaining a part of the scientific data. We gratefully acknowledge Lindy Abas for help with ABP1::GFP-ABP1 construct design. This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program [grant agreement no. 742985] and Austrian Science Fund (FWF) [I 3630-B25] to J.F.; DOC Fellowship of the Austrian Academy of Sciences to L.L.; the European Structural and Investment Funds, Operational Programme Research, Development and Education - Project „MSCAfellow@MUNI“ [CZ.02.2.69/0.0/0.0/17_050/0008496] to M.P.. This project was also supported by the Czech Science Foundation [GA 20-20860Y] to M.Z and MEYS CR [project no.CZ.02.1.01/0.0/0.0/16_019/0000738] to M. Č. article_number: '110750' article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: Zuzana full_name: Gelová, Zuzana id: 0AE74790-0E0B-11E9-ABC7-1ACFE5697425 last_name: Gelová orcid: 0000-0003-4783-1752 - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: Markéta full_name: Pernisová, Markéta last_name: Pernisová - first_name: Géraldine full_name: Brunoud, Géraldine last_name: Brunoud - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Jaroslav full_name: Michalko, Jaroslav id: 483727CA-F248-11E8-B48F-1D18A9856A87 last_name: Michalko - first_name: Zlata full_name: Pavlovicova, Zlata last_name: Pavlovicova - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Robert full_name: Hauschild, Robert id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87 last_name: Hauschild orcid: 0000-0001-9843-3522 - first_name: Milada full_name: Čovanová, Milada last_name: Čovanová - first_name: Marta full_name: Zwiewka, Marta last_name: Zwiewka - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Tongda full_name: Xu, Tongda last_name: Xu - first_name: Teva full_name: Vernoux, Teva last_name: Vernoux - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Gelová Z, Gallei MC, Pernisová M, et al. Developmental roles of auxin binding protein 1 in Arabidopsis thaliana. Plant Science. 2021;303. doi:10.1016/j.plantsci.2020.110750 apa: Gelová, Z., Gallei, M. C., Pernisová, M., Brunoud, G., Zhang, X., Glanc, M., … Friml, J. (2021). Developmental roles of auxin binding protein 1 in Arabidopsis thaliana. Plant Science. Elsevier. https://doi.org/10.1016/j.plantsci.2020.110750 chicago: Gelová, Zuzana, Michelle C Gallei, Markéta Pernisová, Géraldine Brunoud, Xixi Zhang, Matous Glanc, Lanxin Li, et al. “Developmental Roles of Auxin Binding Protein 1 in Arabidopsis Thaliana.” Plant Science. Elsevier, 2021. https://doi.org/10.1016/j.plantsci.2020.110750. ieee: Z. Gelová et al., “Developmental roles of auxin binding protein 1 in Arabidopsis thaliana,” Plant Science, vol. 303. Elsevier, 2021. ista: Gelová Z, Gallei MC, Pernisová M, Brunoud G, Zhang X, Glanc M, Li L, Michalko J, Pavlovicova Z, Verstraeten I, Han H, Hajny J, Hauschild R, Čovanová M, Zwiewka M, Hörmayer L, Fendrych M, Xu T, Vernoux T, Friml J. 2021. Developmental roles of auxin binding protein 1 in Arabidopsis thaliana. Plant Science. 303, 110750. mla: Gelová, Zuzana, et al. “Developmental Roles of Auxin Binding Protein 1 in Arabidopsis Thaliana.” Plant Science, vol. 303, 110750, Elsevier, 2021, doi:10.1016/j.plantsci.2020.110750. short: Z. Gelová, M.C. Gallei, M. Pernisová, G. Brunoud, X. Zhang, M. Glanc, L. Li, J. Michalko, Z. Pavlovicova, I. Verstraeten, H. Han, J. Hajny, R. Hauschild, M. Čovanová, M. Zwiewka, L. Hörmayer, M. Fendrych, T. Xu, T. Vernoux, J. Friml, Plant Science 303 (2021). date_created: 2020-12-09T14:48:28Z date_published: 2021-02-01T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '01' ddc: - '580' department: - _id: JiFr - _id: Bio doi: 10.1016/j.plantsci.2020.110750 ec_funded: 1 external_id: isi: - '000614154500001' pmid: - '33487339' file: - access_level: open_access checksum: a7f2562bdca62d67dfa88e271b62a629 content_type: application/pdf creator: dernst date_created: 2021-02-04T07:49:25Z date_updated: 2021-02-04T07:49:25Z file_id: '9083' file_name: 2021_PlantScience_Gelova.pdf file_size: 12563728 relation: main_file success: 1 file_date_updated: 2021-02-04T07:49:25Z has_accepted_license: '1' intvolume: ' 303' isi: 1 keyword: - Agronomy and Crop Science - Plant Science - Genetics - General Medicine language: - iso: eng month: '02' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 26B4D67E-B435-11E9-9278-68D0E5697425 grant_number: '25351' name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated Rapid Growth Inhibition in Arabidopsis Root' publication: Plant Science publication_identifier: issn: - 0168-9452 publication_status: published publisher: Elsevier quality_controlled: '1' related_material: record: - id: '11626' relation: dissertation_contains status: public - id: '10083' relation: dissertation_contains status: public scopus_import: '1' status: public title: Developmental roles of auxin binding protein 1 in Arabidopsis thaliana tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 303 year: '2021' ... --- _id: '9287' abstract: - lang: eng text: "The phytohormone auxin and its directional transport through tissues are intensively studied. However, a mechanistic understanding of auxin-mediated feedback on endocytosis and polar distribution of PIN auxin transporters remains limited due to contradictory observations and interpretations. Here, we used state-of-the-art methods to reexamine the\r\nauxin effects on PIN endocytic trafficking. We used high auxin concentrations or longer treatments versus lower concentrations and shorter treatments of natural (IAA) and synthetic (NAA) auxins to distinguish between specific and nonspecific effects. Longer treatments of both auxins interfere with Brefeldin A-mediated intracellular PIN2 accumulation and also with general aggregation of endomembrane compartments. NAA treatment decreased the internalization of the endocytic tracer dye, FM4-64; however, NAA treatment also affected the number, distribution, and compartment identity of the early endosome/trans-Golgi network (EE/TGN), rendering the FM4-64 endocytic assays at high NAA concentrations unreliable. To circumvent these nonspecific effects of NAA and IAA affecting the endomembrane system, we opted for alternative approaches visualizing the endocytic events directly at the plasma membrane (PM). Using Total Internal Reflection Fluorescence (TIRF) microscopy, we saw no significant effects of IAA or NAA treatments on the incidence and dynamics of clathrin foci, implying that these treatments do not affect the overall endocytosis rate. However, both NAA and IAA at low concentrations rapidly and specifically promoted endocytosis of photo-converted PIN2 from the PM. These analyses identify a specific effect of NAA and IAA on PIN2 endocytosis, thus contributing to its\r\npolarity maintenance and furthermore illustrate that high auxin levels have nonspecific effects on trafficking and endomembrane compartments. " acknowledged_ssus: - _id: M-Shop - _id: Bio acknowledgement: 'We thank Ivan Kulik for developing the Chip’n’Dale apparatus with Lanxin Li; the IST machine shop and the Bioimaging facility for their excellent support; Matouš Glanc and Matyáš Fendrych for their valuable discussions and help; Barbara Casillas-Perez for her help with statistics. This project has received funding from the European Research Council (ERC) under the European Union''s Horizon 2020 research and innovation program (grant agreement No 742985). A.J. is supported by funding from the Austrian Science Fund (FWF): I3630B25 to J.F. ' article_processing_charge: Yes (in subscription journal) article_type: original author: - first_name: Madhumitha full_name: Narasimhan, Madhumitha id: 44BF24D0-F248-11E8-B48F-1D18A9856A87 last_name: Narasimhan orcid: 0000-0002-8600-0671 - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: E full_name: Himschoot, E last_name: Himschoot - first_name: R full_name: Wang, R last_name: Wang - first_name: S full_name: Vanneste, S last_name: Vanneste - first_name: J full_name: Sánchez-Simarro, J last_name: Sánchez-Simarro - first_name: F full_name: Aniento, F last_name: Aniento - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Narasimhan M, Gallei MC, Tan S, et al. Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking. Plant Physiology. 2021;186(2):1122–1142. doi:10.1093/plphys/kiab134 apa: Narasimhan, M., Gallei, M. C., Tan, S., Johnson, A. J., Verstraeten, I., Li, L., … Friml, J. (2021). Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking. Plant Physiology. Oxford University Press. https://doi.org/10.1093/plphys/kiab134 chicago: Narasimhan, Madhumitha, Michelle C Gallei, Shutang Tan, Alexander J Johnson, Inge Verstraeten, Lanxin Li, Lesia Rodriguez Solovey, et al. “Systematic Analysis of Specific and Nonspecific Auxin Effects on Endocytosis and Trafficking.” Plant Physiology. Oxford University Press, 2021. https://doi.org/10.1093/plphys/kiab134. ieee: M. Narasimhan et al., “Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking,” Plant Physiology, vol. 186, no. 2. Oxford University Press, pp. 1122–1142, 2021. ista: Narasimhan M, Gallei MC, Tan S, Johnson AJ, Verstraeten I, Li L, Rodriguez Solovey L, Han H, Himschoot E, Wang R, Vanneste S, Sánchez-Simarro J, Aniento F, Adamowski M, Friml J. 2021. Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking. Plant Physiology. 186(2), 1122–1142. mla: Narasimhan, Madhumitha, et al. “Systematic Analysis of Specific and Nonspecific Auxin Effects on Endocytosis and Trafficking.” Plant Physiology, vol. 186, no. 2, Oxford University Press, 2021, pp. 1122–1142, doi:10.1093/plphys/kiab134. short: M. Narasimhan, M.C. Gallei, S. Tan, A.J. Johnson, I. Verstraeten, L. Li, L. Rodriguez Solovey, H. Han, E. Himschoot, R. Wang, S. Vanneste, J. Sánchez-Simarro, F. Aniento, M. Adamowski, J. Friml, Plant Physiology 186 (2021) 1122–1142. date_created: 2021-03-26T12:08:38Z date_published: 2021-06-01T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1093/plphys/kiab134 ec_funded: 1 external_id: isi: - '000671555900031' pmid: - '33734402' file: - access_level: open_access checksum: 532bb9469d3b665907f06df8c383eade content_type: application/pdf creator: cziletti date_created: 2021-11-11T15:07:51Z date_updated: 2021-11-11T15:07:51Z file_id: '10273' file_name: 2021_PlantPhysio_Narasimhan.pdf file_size: 2289127 relation: main_file success: 1 file_date_updated: 2021-11-11T15:07:51Z has_accepted_license: '1' intvolume: ' 186' isi: 1 issue: '2' language: - iso: eng month: '06' oa: 1 oa_version: Published Version page: 1122–1142 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: Oxford University Press quality_controlled: '1' related_material: link: - relation: erratum url: 10.1093/plphys/kiab380 record: - id: '11626' relation: dissertation_contains status: public - id: '10083' relation: dissertation_contains status: public status: public title: Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 186 year: '2021' ... --- _id: '10083' abstract: - lang: eng text: "Plant motions occur across a wide spectrum of timescales, ranging from seed dispersal through bursting (milliseconds) and stomatal opening (minutes) to long-term adaptation of gross architecture. Relatively fast motions include water-driven growth as exemplified by root cell expansion under abiotic/biotic stresses or during gravitropism. A showcase is a root growth inhibition in 30 seconds triggered by the phytohormone auxin. However, the cellular and molecular mechanisms are still largely unknown. This thesis covers the studies about this topic as follows. By taking advantage of microfluidics combined with live imaging, pharmaceutical tools, and transgenic lines, we examined the kinetics of and causal relationship among various auxininduced rapid cellular changes in root growth, apoplastic pH, cytosolic Ca2+, cortical microtubule (CMT) orientation, and vacuolar morphology. We revealed that CMT reorientation and vacuolar constriction are the consequence of growth itself instead of responding directly to auxin. In contrast, auxin induces apoplast alkalinization to rapidly inhibit root growth in 30 seconds. This auxin-triggered apoplast alkalinization results from rapid H+- influx that is contributed by Ca2+ inward channel CYCLIC NUCLEOTIDE-GATED CHANNEL 14 (CNGC14)-dependent Ca2+ signaling. To dissect which auxin signaling mediates the rapid apoplast alkalinization, we\r\ncombined microfluidics and genetic engineering to verify that TIR1/AFB receptors conduct a non-transcriptional regulation on Ca2+ and H+ -influx. This non-canonical pathway is mostly mediated by the cytosolic portion of TIR1/AFB. On the other hand, we uncovered, using biochemical and phospho-proteomic analysis, that auxin cell surface signaling component TRANSMEMBRANE KINASE 1 (TMK1) plays a negative role during auxin-trigger apoplast\r\nalkalinization and root growth inhibition through directly activating PM H+ -ATPases. Therefore, we discovered that PM H+ -ATPases counteract instead of mediate the auxintriggered rapid H+ -influx, and that TIR1/AFB and TMK1 regulate root growth antagonistically. This opposite effect of TIR1/AFB and TMK1 is consistent during auxin-induced hypocotyl elongation, leading us to explore the relation of two signaling pathways. Assisted with biochemistry and fluorescent imaging, we verified for the first time that TIR1/AFB and TMK1 can interact with each other. The ability of TIR1/AFB binding to membrane lipid provides a basis for the interaction of plasma membrane- and cytosol-localized proteins.\r\nBesides, transgenic analysis combined with genetic engineering and biochemistry showed that vi\r\nthey do function in the same pathway. Particularly, auxin-induced TMK1 increase is TIR1/AFB dependent, suggesting TIR1/AFB regulation on TMK1. Conversely, TMK1 also regulates TIR1/AFB protein levels and thus auxin canonical signaling. To follow the study of rapid growth regulation, we analyzed another rapid growth regulator, signaling peptide RALF1. We showed that RALF1 also triggers a rapid and reversible growth inhibition caused by H + influx, highly resembling but not dependent on auxin. Besides, RALF1 promotes auxin biosynthesis by increasing expression of auxin biosynthesis enzyme YUCCAs and thus induces auxin signaling in ca. 1 hour, contributing to the sustained RALF1-triggered growth inhibition. These studies collectively contribute to understanding rapid regulation on plant cell\r\ngrowth, novel auxin signaling pathway as well as auxin-peptide crosstalk. " alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Lanxin full_name: Li, Lanxin last_name: Li citation: ama: Li L. Rapid cell growth regulation in Arabidopsis. 2021. doi:10.15479/at:ista:10083 apa: Li, L. (2021). Rapid cell growth regulation in Arabidopsis. Institute of Science and Technology Austria. https://doi.org/10.15479/at:ista:10083 chicago: Li, Lanxin. “Rapid Cell Growth Regulation in Arabidopsis.” Institute of Science and Technology Austria, 2021. https://doi.org/10.15479/at:ista:10083. ieee: L. Li, “Rapid cell growth regulation in Arabidopsis,” Institute of Science and Technology Austria, 2021. ista: Li L. 2021. Rapid cell growth regulation in Arabidopsis. Institute of Science and Technology Austria. mla: Li, Lanxin. Rapid Cell Growth Regulation in Arabidopsis. Institute of Science and Technology Austria, 2021, doi:10.15479/at:ista:10083. short: L. Li, Rapid Cell Growth Regulation in Arabidopsis, Institute of Science and Technology Austria, 2021. date_created: 2021-10-04T13:33:10Z date_published: 2021-10-06T00:00:00Z date_updated: 2023-10-31T19:30:02Z day: '06' ddc: - '575' degree_awarded: PhD department: - _id: GradSch - _id: JiFr doi: 10.15479/at:ista:10083 ec_funded: 1 file: - access_level: open_access checksum: 3b2f55b3b8ae05337a0dcc1cd8595b10 content_type: application/pdf creator: cchlebak date_created: 2021-10-14T08:00:07Z date_updated: 2022-12-20T23:30:03Z embargo: 2022-10-14 file_id: '10138' file_name: 0._IST_Austria_Thesis_Lanxin_Li_1014_pdftron.pdf file_size: 8616142 relation: main_file - access_level: closed checksum: f23ed258ca894f6aabf58b0c128bf242 content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: cchlebak date_created: 2021-10-14T08:00:13Z date_updated: 2022-12-20T23:30:03Z embargo_to: open_access file_id: '10139' file_name: 0._IST_Austria_Thesis_Lanxin_Li_1014.docx file_size: 15058499 relation: source_file file_date_updated: 2022-12-20T23:30:03Z has_accepted_license: '1' language: - iso: eng month: '10' oa: 1 oa_version: Published Version project: - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program - _id: 26B4D67E-B435-11E9-9278-68D0E5697425 grant_number: '25351' name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated Rapid Growth Inhibition in Arabidopsis Root' publication_identifier: issn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '442' relation: part_of_dissertation status: public - id: '8931' relation: part_of_dissertation status: public - id: '9287' relation: part_of_dissertation status: public - id: '8283' relation: part_of_dissertation status: public - id: '8986' relation: part_of_dissertation status: public - id: '6627' relation: part_of_dissertation status: public - id: '10095' relation: part_of_dissertation status: public - id: '10015' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: Rapid cell growth regulation in Arabidopsis tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2021' ... --- _id: '10015' abstract: - lang: eng text: "Auxin plays a dual role in growth regulation and, depending on the tissue and concentration of the hormone, it can either promote or inhibit division and expansion processes in plants. Recent studies have revealed that, beyond transcriptional reprogramming, alternative auxincontrolled mechanisms regulate root growth. Here, we explored the impact of different concentrations of the synthetic auxin NAA that establish growth-promoting and -repressing conditions on the root tip proteome and phosphoproteome, generating a unique resource. From the phosphoproteome data, we pinpointed (novel) growth regulators, such as the RALF34-THE1 module. Our results, together with previously published studies, suggest that auxin, H+-ATPases, cell wall modifications and cell wall sensing receptor-like kinases are tightly embedded in a pathway regulating cell elongation. Furthermore, our study assigned a novel role to MKK2 as a regulator of primary root growth and a (potential) regulator of auxin biosynthesis and signalling, and suggests the importance of the MKK2\r\nThr31 phosphorylation site for growth regulation in the Arabidopsis root tip." acknowledgement: We thank the Nottingham Stock Centre for seeds, Frank Van Breusegem for the phb3 mutant, and Herman Höfte for the the1 mutant. Open Access Funding by the Austrian Science Fund (FWF). alternative_title: - Protein Phosphorylation and Cell Signaling in Plants article_number: '1665 ' article_processing_charge: Yes article_type: original author: - first_name: N full_name: Nikonorova, N last_name: Nikonorova - first_name: E full_name: Murphy, E last_name: Murphy - first_name: CF full_name: Fonseca de Lima, CF last_name: Fonseca de Lima - first_name: S full_name: Zhu, S last_name: Zhu - first_name: B full_name: van de Cotte, B last_name: van de Cotte - first_name: LD full_name: Vu, LD last_name: Vu - first_name: D full_name: Balcerowicz, D last_name: Balcerowicz - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: X full_name: Kong, X last_name: Kong - first_name: G full_name: De Rop, G last_name: De Rop - first_name: T full_name: Beeckman, T last_name: Beeckman - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: K full_name: Vissenberg, K last_name: Vissenberg - first_name: PC full_name: Morris, PC last_name: Morris - first_name: Z full_name: Ding, Z last_name: Ding - first_name: I full_name: De Smet, I last_name: De Smet citation: ama: Nikonorova N, Murphy E, Fonseca de Lima C, et al. The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators. Cells. 2021;10. doi:10.3390/cells10071665 apa: Nikonorova, N., Murphy, E., Fonseca de Lima, C., Zhu, S., van de Cotte, B., Vu, L., … De Smet, I. (2021). The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators. Cells. MDPI. https://doi.org/10.3390/cells10071665 chicago: Nikonorova, N, E Murphy, CF Fonseca de Lima, S Zhu, B van de Cotte, LD Vu, D Balcerowicz, et al. “The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators.” Cells. MDPI, 2021. https://doi.org/10.3390/cells10071665. ieee: N. Nikonorova et al., “The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators,” Cells, vol. 10. MDPI, 2021. ista: Nikonorova N, Murphy E, Fonseca de Lima C, Zhu S, van de Cotte B, Vu L, Balcerowicz D, Li L, Kong X, De Rop G, Beeckman T, Friml J, Vissenberg K, Morris P, Ding Z, De Smet I. 2021. The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators. Cells. 10, 1665. mla: Nikonorova, N., et al. “The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators.” Cells, vol. 10, 1665, MDPI, 2021, doi:10.3390/cells10071665. short: N. Nikonorova, E. Murphy, C. Fonseca de Lima, S. Zhu, B. van de Cotte, L. Vu, D. Balcerowicz, L. Li, X. Kong, G. De Rop, T. Beeckman, J. Friml, K. Vissenberg, P. Morris, Z. Ding, I. De Smet, Cells 10 (2021). date_created: 2021-09-14T11:36:20Z date_published: 2021-07-02T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '02' ddc: - '575' department: - _id: JiFr doi: 10.3390/cells10071665 ec_funded: 1 external_id: isi: - '000676604700001' pmid: - '34359847' file: - access_level: open_access checksum: 2a9f534b9c2200e72e2cde95afaf4eed content_type: application/pdf creator: cchlebak date_created: 2021-09-16T09:07:06Z date_updated: 2021-09-16T09:07:06Z file_id: '10021' file_name: 2021_Cells_Nikonorova.pdf file_size: 2667848 relation: main_file success: 1 file_date_updated: 2021-09-16T09:07:06Z has_accepted_license: '1' intvolume: ' 10' isi: 1 keyword: - primary root - (phospho)proteomics - auxin - (receptor) kinase language: - iso: eng month: '07' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program - _id: 3AC91DDA-15DF-11EA-824D-93A3E7B544D1 call_identifier: FWF name: FWF Open Access Fund publication: Cells publication_identifier: issn: - 2073-4409 publication_status: published publisher: MDPI quality_controlled: '1' related_material: record: - id: '10083' relation: dissertation_contains status: public status: public title: The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 10 year: '2021' ... --- _id: '10095' abstract: - lang: eng text: Growth regulation tailors plant development to its environment. A showcase is response to gravity, where shoots bend up and roots down1. This paradox is based on opposite effects of the phytohormone auxin, which promotes cell expansion in shoots, while inhibiting it in roots via a yet unknown cellular mechanism2. Here, by combining microfluidics, live imaging, genetic engineering and phospho-proteomics in Arabidopsis thaliana, we advance our understanding how auxin inhibits root growth. We show that auxin activates two distinct, antagonistically acting signalling pathways that converge on the rapid regulation of the apoplastic pH, a causative growth determinant. Cell surface-based TRANSMEMBRANE KINASE1 (TMK1) interacts with and mediates phosphorylation and activation of plasma membrane H+-ATPases for apoplast acidification, while intracellular canonical auxin signalling promotes net cellular H+-influx, causing apoplast alkalinisation. The simultaneous activation of these two counteracting mechanisms poises the root for a rapid, fine-tuned growth modulation while navigating complex soil environment. acknowledged_ssus: - _id: LifeSc - _id: M-Shop - _id: Bio acknowledgement: We thank Nataliia Gnyliukh and Lukas Hörmayer for technical assistance and Nadine Paris for sharing PM-Cyto seeds. We gratefully acknowledge Life Science, Machine Shop and Bioimaging Facilities of IST Austria. This project has received funding from the European Research Council Advanced Grant (ETAP-742985) and the Austrian Science Fund (FWF) I 3630-B25 to J.F., the National Institutes of Health (GM067203) to W.M.G., the Netherlands Organization for Scientific Research (NWO; VIDI-864.13.001.), the Research Foundation-Flanders (FWO; Odysseus II G0D0515N) and a European Research Council Starting Grant (TORPEDO-714055) to W.S. and B.D.R., the VICI grant (865.14.001) from the Netherlands Organization for Scientific Research to M.R and D.W., the Australian Research Council and China National Distinguished Expert Project (WQ20174400441) to S.S., the MEXT/JSPS KAKENHI to K.T. (20K06685) and T.K. (20H05687 and 20H05910), the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie Grant Agreement No. 665385 and the DOC Fellowship of the Austrian Academy of Sciences to L.L., the China Scholarship Council to J.C. article_number: '266395' article_processing_charge: No author: - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Mark full_name: Roosjen, Mark last_name: Roosjen - first_name: Koji full_name: Takahashi, Koji last_name: Takahashi - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Jack full_name: Merrin, Jack id: 4515C308-F248-11E8-B48F-1D18A9856A87 last_name: Merrin orcid: 0000-0001-5145-4609 - first_name: Jian full_name: Chen, Jian last_name: Chen - first_name: Lana full_name: Shabala, Lana last_name: Shabala - first_name: Wouter full_name: Smet, Wouter last_name: Smet - first_name: Hong full_name: Ren, Hong last_name: Ren - first_name: Steffen full_name: Vanneste, Steffen last_name: Vanneste - first_name: Sergey full_name: Shabala, Sergey last_name: Shabala - first_name: Bert full_name: De Rybel, Bert last_name: De Rybel - first_name: Dolf full_name: Weijers, Dolf last_name: Weijers - first_name: Toshinori full_name: Kinoshita, Toshinori last_name: Kinoshita - first_name: William M. full_name: Gray, William M. last_name: Gray - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Li L, Verstraeten I, Roosjen M, et al. Cell surface and intracellular auxin signalling for H+-fluxes in root growth. Research Square. doi:10.21203/rs.3.rs-266395/v3 apa: Li, L., Verstraeten, I., Roosjen, M., Takahashi, K., Rodriguez Solovey, L., Merrin, J., … Friml, J. (n.d.). Cell surface and intracellular auxin signalling for H+-fluxes in root growth. Research Square. https://doi.org/10.21203/rs.3.rs-266395/v3 chicago: Li, Lanxin, Inge Verstraeten, Mark Roosjen, Koji Takahashi, Lesia Rodriguez Solovey, Jack Merrin, Jian Chen, et al. “Cell Surface and Intracellular Auxin Signalling for H+-Fluxes in Root Growth.” Research Square, n.d. https://doi.org/10.21203/rs.3.rs-266395/v3. ieee: L. Li et al., “Cell surface and intracellular auxin signalling for H+-fluxes in root growth,” Research Square. . ista: Li L, Verstraeten I, Roosjen M, Takahashi K, Rodriguez Solovey L, Merrin J, Chen J, Shabala L, Smet W, Ren H, Vanneste S, Shabala S, De Rybel B, Weijers D, Kinoshita T, Gray WM, Friml J. Cell surface and intracellular auxin signalling for H+-fluxes in root growth. Research Square, 266395. mla: Li, Lanxin, et al. “Cell Surface and Intracellular Auxin Signalling for H+-Fluxes in Root Growth.” Research Square, 266395, doi:10.21203/rs.3.rs-266395/v3. short: L. Li, I. Verstraeten, M. Roosjen, K. Takahashi, L. Rodriguez Solovey, J. Merrin, J. Chen, L. Shabala, W. Smet, H. Ren, S. Vanneste, S. Shabala, B. De Rybel, D. Weijers, T. Kinoshita, W.M. Gray, J. Friml, Research Square (n.d.). date_created: 2021-10-06T08:56:22Z date_published: 2021-09-09T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '09' department: - _id: JiFr - _id: NanoFab doi: 10.21203/rs.3.rs-266395/v3 ec_funded: 1 language: - iso: eng main_file_link: - open_access: '1' url: https://www.doi.org/10.21203/rs.3.rs-266395/v3 month: '09' oa: 1 oa_version: Preprint project: - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 26B4D67E-B435-11E9-9278-68D0E5697425 grant_number: '25351' name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated Rapid Growth Inhibition in Arabidopsis Root' publication: Research Square publication_identifier: issn: - 2693-5015 publication_status: accepted related_material: record: - id: '10223' relation: later_version status: public - id: '10083' relation: dissertation_contains status: public status: public title: Cell surface and intracellular auxin signalling for H+-fluxes in root growth tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: preprint user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 year: '2021' ... --- _id: '7601' abstract: - lang: eng text: Plasmodesmata (PD) are crucial structures for intercellular communication in multicellular plants with remorins being their crucial plant-specific structural and functional constituents. The PD biogenesis is an intriguing but poorly understood process. By expressing an Arabidopsis remorin protein in mammalian cells, we have reconstituted a PD-like filamentous structure, termed remorin filament (RF), connecting neighboring cells physically and physiologically. Notably, RFs are capable of transporting macromolecules intercellularly, in a way similar to plant PD. With further super-resolution microscopic analysis and biochemical characterization, we found that RFs are also composed of actin filaments, forming the core skeleton structure, aligned with the remorin protein. This unique heterologous filamentous structure might explain the molecular mechanism for remorin function as well as PD construction. Furthermore, remorin protein exhibits a specific distribution manner in the plasma membrane in mammalian cells, representing a lipid nanodomain, depending on its lipid modification status. Our studies not only provide crucial insights into the mechanism of PD biogenesis, but also uncovers unsuspected fundamental mechanistic and evolutionary links between intercellular communication systems of plants and animals. article_processing_charge: No author: - first_name: Zhuang full_name: Wei, Zhuang last_name: Wei - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Tao full_name: Liu, Tao last_name: Liu - first_name: Yuan full_name: Wu, Yuan last_name: Wu - first_name: Ji-Gang full_name: Lei, Ji-Gang last_name: Lei - first_name: ZhengJun full_name: Chen, ZhengJun last_name: Chen - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Hong-Wei full_name: Xue, Hong-Wei last_name: Xue - first_name: Kan full_name: Liao, Kan last_name: Liao citation: ama: Wei Z, Tan S, Liu T, et al. Plasmodesmata-like intercellular connections by plant remorin in animal cells. bioRxiv. 2020. doi:10.1101/791137 apa: Wei, Z., Tan, S., Liu, T., Wu, Y., Lei, J.-G., Chen, Z., … Liao, K. (2020). Plasmodesmata-like intercellular connections by plant remorin in animal cells. bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/791137 chicago: Wei, Zhuang, Shutang Tan, Tao Liu, Yuan Wu, Ji-Gang Lei, ZhengJun Chen, Jiří Friml, Hong-Wei Xue, and Kan Liao. “Plasmodesmata-like Intercellular Connections by Plant Remorin in Animal Cells.” BioRxiv. Cold Spring Harbor Laboratory, 2020. https://doi.org/10.1101/791137. ieee: Z. Wei et al., “Plasmodesmata-like intercellular connections by plant remorin in animal cells,” bioRxiv. Cold Spring Harbor Laboratory, 2020. ista: Wei Z, Tan S, Liu T, Wu Y, Lei J-G, Chen Z, Friml J, Xue H-W, Liao K. 2020. Plasmodesmata-like intercellular connections by plant remorin in animal cells. bioRxiv, 10.1101/791137. mla: Wei, Zhuang, et al. “Plasmodesmata-like Intercellular Connections by Plant Remorin in Animal Cells.” BioRxiv, Cold Spring Harbor Laboratory, 2020, doi:10.1101/791137. short: Z. Wei, S. Tan, T. Liu, Y. Wu, J.-G. Lei, Z. Chen, J. Friml, H.-W. Xue, K. Liao, BioRxiv (2020). date_created: 2020-03-21T16:34:42Z date_published: 2020-02-19T00:00:00Z date_updated: 2021-01-12T08:14:26Z day: '19' department: - _id: JiFr doi: 10.1101/791137 language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1101/791137 month: '02' oa: 1 oa_version: Preprint page: '22' publication: bioRxiv publication_status: published publisher: Cold Spring Harbor Laboratory status: public title: Plasmodesmata-like intercellular connections by plant remorin in animal cells type: preprint user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 year: '2020' ... --- _id: '6997' article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang Y, Friml J. Auxin guides roots to avoid obstacles during gravitropic growth. New Phytologist. 2020;225(3):1049-1052. doi:10.1111/nph.16203 apa: Zhang, Y., & Friml, J. (2020). Auxin guides roots to avoid obstacles during gravitropic growth. New Phytologist. Wiley. https://doi.org/10.1111/nph.16203 chicago: Zhang, Yuzhou, and Jiří Friml. “Auxin Guides Roots to Avoid Obstacles during Gravitropic Growth.” New Phytologist. Wiley, 2020. https://doi.org/10.1111/nph.16203. ieee: Y. Zhang and J. Friml, “Auxin guides roots to avoid obstacles during gravitropic growth,” New Phytologist, vol. 225, no. 3. Wiley, pp. 1049–1052, 2020. ista: Zhang Y, Friml J. 2020. Auxin guides roots to avoid obstacles during gravitropic growth. New Phytologist. 225(3), 1049–1052. mla: Zhang, Yuzhou, and Jiří Friml. “Auxin Guides Roots to Avoid Obstacles during Gravitropic Growth.” New Phytologist, vol. 225, no. 3, Wiley, 2020, pp. 1049–52, doi:10.1111/nph.16203. short: Y. Zhang, J. Friml, New Phytologist 225 (2020) 1049–1052. date_created: 2019-11-12T11:41:32Z date_published: 2020-02-01T00:00:00Z date_updated: 2023-08-17T14:01:49Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/nph.16203 ec_funded: 1 external_id: isi: - '000489638800001' pmid: - '31603260' file: - access_level: open_access checksum: cd42ffdb381fd52812b9583d4d407139 content_type: application/pdf creator: dernst date_created: 2020-11-18T16:42:48Z date_updated: 2020-11-18T16:42:48Z file_id: '8772' file_name: 2020_NewPhytologist_Zhang.pdf file_size: 717345 relation: main_file success: 1 file_date_updated: 2020-11-18T16:42:48Z has_accepted_license: '1' intvolume: ' 225' isi: 1 issue: '3' language: - iso: eng month: '02' oa: 1 oa_version: Published Version page: 1049-1052 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646x publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Auxin guides roots to avoid obstacles during gravitropic growth tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 225 year: '2020' ... --- _id: '7204' abstract: - lang: eng text: Plant root architecture dynamically adapts to various environmental conditions, such as salt‐containing soil. The phytohormone abscisic acid (ABA) is involved among others also in these developmental adaptations, but the underlying molecular mechanism remains elusive. Here, a novel branch of the ABA signaling pathway in Arabidopsis involving PYR/PYL/RCAR (abbreviated as PYLs) receptor‐protein phosphatase 2A (PP2A) complex that acts in parallel to the canonical PYLs‐protein phosphatase 2C (PP2C) mechanism is identified. The PYLs‐PP2A signaling modulates root gravitropism and lateral root formation through regulating phytohormone auxin transport. In optimal conditions, PYLs ABA receptor interacts with the catalytic subunits of PP2A, increasing their phosphatase activity and thus counteracting PINOID (PID) kinase‐mediated phosphorylation of PIN‐FORMED (PIN) auxin transporters. By contrast, in salt and osmotic stress conditions, ABA binds to PYLs, inhibiting the PP2A activity, which leads to increased PIN phosphorylation and consequently modulated directional auxin transport leading to adapted root architecture. This work reveals an adaptive mechanism that may flexibly adjust plant root growth to withstand saline and osmotic stresses. It occurs via the cross‐talk between the stress hormone ABA and the versatile developmental regulator auxin. article_number: '1901455' article_processing_charge: No article_type: original author: - first_name: Yang full_name: Li, Yang last_name: Li - first_name: Yaping full_name: Wang, Yaping last_name: Wang - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Zhen full_name: Li, Zhen last_name: Li - first_name: Zhi full_name: Yuan, Zhi last_name: Yuan - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: David full_name: Domjan, David id: C684CD7A-257E-11EA-9B6F-D8588B4F947F last_name: Domjan orcid: 0000-0003-2267-106X - first_name: Kai full_name: Wang, Kai last_name: Wang - first_name: Wei full_name: Xuan, Wei last_name: Xuan - first_name: Yan full_name: Guo, Yan last_name: Guo - first_name: Zhizhong full_name: Gong, Zhizhong last_name: Gong - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Jing full_name: Zhang, Jing last_name: Zhang citation: ama: Li Y, Wang Y, Tan S, et al. Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex. Advanced Science. 2020;7(3). doi:10.1002/advs.201901455 apa: Li, Y., Wang, Y., Tan, S., Li, Z., Yuan, Z., Glanc, M., … Zhang, J. (2020). Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex. Advanced Science. Wiley. https://doi.org/10.1002/advs.201901455 chicago: Li, Yang, Yaping Wang, Shutang Tan, Zhen Li, Zhi Yuan, Matous Glanc, David Domjan, et al. “Root Growth Adaptation Is Mediated by PYLs ABA Receptor-PP2A Protein Phosphatase Complex.” Advanced Science. Wiley, 2020. https://doi.org/10.1002/advs.201901455. ieee: Y. Li et al., “Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex,” Advanced Science, vol. 7, no. 3. Wiley, 2020. ista: Li Y, Wang Y, Tan S, Li Z, Yuan Z, Glanc M, Domjan D, Wang K, Xuan W, Guo Y, Gong Z, Friml J, Zhang J. 2020. Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex. Advanced Science. 7(3), 1901455. mla: Li, Yang, et al. “Root Growth Adaptation Is Mediated by PYLs ABA Receptor-PP2A Protein Phosphatase Complex.” Advanced Science, vol. 7, no. 3, 1901455, Wiley, 2020, doi:10.1002/advs.201901455. short: Y. Li, Y. Wang, S. Tan, Z. Li, Z. Yuan, M. Glanc, D. Domjan, K. Wang, W. Xuan, Y. Guo, Z. Gong, J. Friml, J. Zhang, Advanced Science 7 (2020). date_created: 2019-12-22T23:00:43Z date_published: 2020-02-05T00:00:00Z date_updated: 2023-08-17T14:13:17Z day: '05' ddc: - '580' department: - _id: JiFr doi: 10.1002/advs.201901455 external_id: isi: - '000501912800001' pmid: - '32042554' file: - access_level: open_access checksum: 016eeab5860860af038e2da95ffe75c3 content_type: application/pdf creator: dernst date_created: 2020-02-24T14:29:54Z date_updated: 2020-07-14T12:47:53Z file_id: '7519' file_name: 2020_AdvScience_Li.pdf file_size: 3586924 relation: main_file file_date_updated: 2020-07-14T12:47:53Z has_accepted_license: '1' intvolume: ' 7' isi: 1 issue: '3' language: - iso: eng month: '02' oa: 1 oa_version: Published Version pmid: 1 publication: Advanced Science publication_identifier: eissn: - 2198-3844 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 7 year: '2020' ... --- _id: '7142' abstract: - lang: eng text: The phytohormone auxin acts as an amazingly versatile coordinator of plant growth and development. With its morphogen-like properties, auxin controls sites and timing of differentiation and/or growth responses both, in quantitative and qualitative terms. Specificity in the auxin response depends largely on distinct modes of signal transmission, by which individual cells perceive and convert auxin signals into a remarkable diversity of responses. The best understood, or so-called canonical mechanism of auxin perception ultimately results in variable adjustments of the cellular transcriptome, via a short, nuclear signal transduction pathway. Additional findings that accumulated over decades implied that an additional, presumably, cell surface-based auxin perception mechanism mediates very rapid cellular responses and decisively contributes to the cell's overall hormonal response. Recent investigations into both, nuclear and cell surface auxin signalling challenged this assumed partition of roles for different auxin signalling pathways and revealed an unexpected complexity in transcriptional and non-transcriptional cellular responses mediated by auxin. acknowledgement: Research in J.F. laboratory is funded by the European Union's Horizon 2020 program (ERC grant agreement n° 742985); C.L. is supported by the Austrian Science Fund (FWF grant P 31493). article_processing_charge: No article_type: original author: - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: Christian full_name: Luschnig, Christian last_name: Luschnig - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: 'Gallei MC, Luschnig C, Friml J. Auxin signalling in growth: Schrödinger’s cat out of the bag. Current Opinion in Plant Biology. 2020;53(2):43-49. doi:10.1016/j.pbi.2019.10.003' apa: 'Gallei, M. C., Luschnig, C., & Friml, J. (2020). Auxin signalling in growth: Schrödinger’s cat out of the bag. Current Opinion in Plant Biology. Elsevier. https://doi.org/10.1016/j.pbi.2019.10.003' chicago: 'Gallei, Michelle C, Christian Luschnig, and Jiří Friml. “Auxin Signalling in Growth: Schrödinger’s Cat out of the Bag.” Current Opinion in Plant Biology. Elsevier, 2020. https://doi.org/10.1016/j.pbi.2019.10.003.' ieee: 'M. C. Gallei, C. Luschnig, and J. Friml, “Auxin signalling in growth: Schrödinger’s cat out of the bag,” Current Opinion in Plant Biology, vol. 53, no. 2. Elsevier, pp. 43–49, 2020.' ista: 'Gallei MC, Luschnig C, Friml J. 2020. Auxin signalling in growth: Schrödinger’s cat out of the bag. Current Opinion in Plant Biology. 53(2), 43–49.' mla: 'Gallei, Michelle C., et al. “Auxin Signalling in Growth: Schrödinger’s Cat out of the Bag.” Current Opinion in Plant Biology, vol. 53, no. 2, Elsevier, 2020, pp. 43–49, doi:10.1016/j.pbi.2019.10.003.' short: M.C. Gallei, C. Luschnig, J. Friml, Current Opinion in Plant Biology 53 (2020) 43–49. date_created: 2019-12-02T12:05:26Z date_published: 2020-02-01T00:00:00Z date_updated: 2023-08-17T14:07:22Z day: '01' department: - _id: JiFr doi: 10.1016/j.pbi.2019.10.003 ec_funded: 1 external_id: isi: - '000521120600007' pmid: - '31760231' intvolume: ' 53' isi: 1 issue: '2' language: - iso: eng month: '02' oa_version: None page: 43-49 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Current Opinion in Plant Biology publication_identifier: eissn: - 1879-0356 issn: - 1369-5266 publication_status: published publisher: Elsevier quality_controlled: '1' related_material: record: - id: '11626' relation: dissertation_contains status: public scopus_import: '1' status: public title: 'Auxin signalling in growth: Schrödinger''s cat out of the bag' type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 53 year: '2020' ... --- _id: '7219' abstract: - lang: eng text: Root system architecture (RSA), governed by the phytohormone auxin, endows plants with an adaptive advantage in particular environments. Using geographically representative arabidopsis (Arabidopsis thaliana) accessions as a resource for GWA mapping, Waidmann et al. and Ogura et al. recently identified two novel components involved in modulating auxin-mediated RSA and conferring plant fitness in particular habitats. article_processing_charge: No article_type: original author: - first_name: Guanghui full_name: Xiao, Guanghui last_name: Xiao - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 citation: ama: 'Xiao G, Zhang Y. Adaptive growth: Shaping auxin-mediated root system architecture. Trends in Plant Science. 2020;25(2):P121-123. doi:10.1016/j.tplants.2019.12.001' apa: 'Xiao, G., & Zhang, Y. (2020). Adaptive growth: Shaping auxin-mediated root system architecture. Trends in Plant Science. Elsevier. https://doi.org/10.1016/j.tplants.2019.12.001' chicago: 'Xiao, Guanghui, and Yuzhou Zhang. “Adaptive Growth: Shaping Auxin-Mediated Root System Architecture.” Trends in Plant Science. Elsevier, 2020. https://doi.org/10.1016/j.tplants.2019.12.001.' ieee: 'G. Xiao and Y. Zhang, “Adaptive growth: Shaping auxin-mediated root system architecture,” Trends in Plant Science, vol. 25, no. 2. Elsevier, pp. P121-123, 2020.' ista: 'Xiao G, Zhang Y. 2020. Adaptive growth: Shaping auxin-mediated root system architecture. Trends in Plant Science. 25(2), P121-123.' mla: 'Xiao, Guanghui, and Yuzhou Zhang. “Adaptive Growth: Shaping Auxin-Mediated Root System Architecture.” Trends in Plant Science, vol. 25, no. 2, Elsevier, 2020, pp. P121-123, doi:10.1016/j.tplants.2019.12.001.' short: G. Xiao, Y. Zhang, Trends in Plant Science 25 (2020) P121-123. date_created: 2019-12-29T23:00:48Z date_published: 2020-02-01T00:00:00Z date_updated: 2023-08-17T14:14:50Z day: '01' department: - _id: JiFr doi: 10.1016/j.tplants.2019.12.001 external_id: isi: - '000508637500001' pmid: - '31843370' intvolume: ' 25' isi: 1 issue: '2' language: - iso: eng month: '02' oa_version: None page: P121-123 pmid: 1 publication: Trends in Plant Science publication_identifier: issn: - '13601385' publication_status: published publisher: Elsevier quality_controlled: '1' scopus_import: '1' status: public title: 'Adaptive growth: Shaping auxin-mediated root system architecture' type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 25 year: '2020' ... --- _id: '7465' abstract: - lang: eng text: The flexible development of plants is characterized by a high capacity for post-embryonic organ formation and tissue regeneration, processes, which require tightly regulated intercellular communication and coordinated tissue (re-)polarization. The phytohormone auxin, the main driver for these processes, is able to establish polarized auxin transport channels, which are characterized by the expression and polar, subcellular localization of the PIN1 auxin transport proteins. These channels are demarcating the position of future vascular strands necessary for organ formation and tissue regeneration. Major progress has been made in the last years to understand how PINs can change their polarity in different contexts and thus guide auxin flow through the plant. However, it still remains elusive how auxin mediates the establishment of auxin conducting channels and the formation of vascular tissue and which cellular processes are involved. By the means of sophisticated regeneration experiments combined with local auxin applications in Arabidopsis thaliana inflorescence stems we show that (i) PIN subcellular dynamics, (ii) PIN internalization by clathrin-mediated trafficking and (iii) an intact actin cytoskeleton required for post-endocytic trafficking are indispensable for auxin channel formation, de novo vascular formation and vascular regeneration after wounding. These observations provide novel insights into cellular mechanism of coordinated tissue polarization during auxin canalization. article_number: '110414' article_processing_charge: No article_type: original author: - first_name: Ewa full_name: Mazur, Ewa last_name: Mazur - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: Hélène S. full_name: Robert, Hélène S. last_name: Robert - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Mazur E, Gallei MC, Adamowski M, Han H, Robert HS, Friml J. Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis. Plant Science. 2020;293(4). doi:10.1016/j.plantsci.2020.110414 apa: Mazur, E., Gallei, M. C., Adamowski, M., Han, H., Robert, H. S., & Friml, J. (2020). Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis. Plant Science. Elsevier. https://doi.org/10.1016/j.plantsci.2020.110414 chicago: Mazur, Ewa, Michelle C Gallei, Maciek Adamowski, Huibin Han, Hélène S. Robert, and Jiří Friml. “Clathrin-Mediated Trafficking and PIN Trafficking Are Required for Auxin Canalization and Vascular Tissue Formation in Arabidopsis.” Plant Science. Elsevier, 2020. https://doi.org/10.1016/j.plantsci.2020.110414. ieee: E. Mazur, M. C. Gallei, M. Adamowski, H. Han, H. S. Robert, and J. Friml, “Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis,” Plant Science, vol. 293, no. 4. Elsevier, 2020. ista: Mazur E, Gallei MC, Adamowski M, Han H, Robert HS, Friml J. 2020. Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis. Plant Science. 293(4), 110414. mla: Mazur, Ewa, et al. “Clathrin-Mediated Trafficking and PIN Trafficking Are Required for Auxin Canalization and Vascular Tissue Formation in Arabidopsis.” Plant Science, vol. 293, no. 4, 110414, Elsevier, 2020, doi:10.1016/j.plantsci.2020.110414. short: E. Mazur, M.C. Gallei, M. Adamowski, H. Han, H.S. Robert, J. Friml, Plant Science 293 (2020). date_created: 2020-02-09T23:00:50Z date_published: 2020-04-01T00:00:00Z date_updated: 2023-08-17T14:37:32Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1016/j.plantsci.2020.110414 ec_funded: 1 external_id: isi: - '000520609800009' file: - access_level: open_access checksum: f7f27c6a8fea985ceb9279be2204461c content_type: application/pdf creator: dernst date_created: 2020-02-10T08:59:36Z date_updated: 2020-07-14T12:47:59Z file_id: '7471' file_name: 2020_PlantScience_Mazur.pdf file_size: 3499069 relation: main_file file_date_updated: 2020-07-14T12:47:59Z has_accepted_license: '1' intvolume: ' 293' isi: 1 issue: '4' language: - iso: eng month: '04' oa: 1 oa_version: Published Version project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Plant Science publication_identifier: eissn: - '18732259' issn: - '01689452' publication_status: published publisher: Elsevier quality_controlled: '1' related_material: record: - id: '11626' relation: dissertation_contains status: public scopus_import: '1' status: public title: Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 293 year: '2020' ... --- _id: '7490' abstract: - lang: eng text: In plants, clathrin mediated endocytosis (CME) represents the major route for cargo internalisation from the cell surface. It has been assumed to operate in an evolutionary conserved manner as in yeast and animals. Here we report characterisation of ultrastructure, dynamics and mechanisms of plant CME as allowed by our advancement in electron microscopy and quantitative live imaging techniques. Arabidopsis CME appears to follow the constant curvature model and the bona fide CME population generates vesicles of a predominantly hexagonal-basket type; larger and with faster kinetics than in other models. Contrary to the existing paradigm, actin is dispensable for CME events at the plasma membrane but plays a unique role in collecting endocytic vesicles, sorting of internalised cargos and directional endosome movement that itself actively promote CME events. Internalized vesicles display a strongly delayed and sequential uncoating. These unique features highlight the independent evolution of the plant CME mechanism during the autonomous rise of multicellularity in eukaryotes. acknowledged_ssus: - _id: LifeSc - _id: Bio - _id: EM-Fac article_number: e52067 article_processing_charge: No article_type: original author: - first_name: Madhumitha full_name: Narasimhan, Madhumitha id: 44BF24D0-F248-11E8-B48F-1D18A9856A87 last_name: Narasimhan orcid: 0000-0002-8600-0671 - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Roshan full_name: Prizak, Roshan id: 4456104E-F248-11E8-B48F-1D18A9856A87 last_name: Prizak - first_name: Walter full_name: Kaufmann, Walter id: 3F99E422-F248-11E8-B48F-1D18A9856A87 last_name: Kaufmann orcid: 0000-0001-9735-5315 - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Barbara E full_name: Casillas Perez, Barbara E id: 351ED2AA-F248-11E8-B48F-1D18A9856A87 last_name: Casillas Perez - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Narasimhan M, Johnson AJ, Prizak R, et al. Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants. eLife. 2020;9. doi:10.7554/eLife.52067 apa: Narasimhan, M., Johnson, A. J., Prizak, R., Kaufmann, W., Tan, S., Casillas Perez, B. E., & Friml, J. (2020). Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants. ELife. eLife Sciences Publications. https://doi.org/10.7554/eLife.52067 chicago: Narasimhan, Madhumitha, Alexander J Johnson, Roshan Prizak, Walter Kaufmann, Shutang Tan, Barbara E Casillas Perez, and Jiří Friml. “Evolutionarily Unique Mechanistic Framework of Clathrin-Mediated Endocytosis in Plants.” ELife. eLife Sciences Publications, 2020. https://doi.org/10.7554/eLife.52067. ieee: M. Narasimhan et al., “Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants,” eLife, vol. 9. eLife Sciences Publications, 2020. ista: Narasimhan M, Johnson AJ, Prizak R, Kaufmann W, Tan S, Casillas Perez BE, Friml J. 2020. Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants. eLife. 9, e52067. mla: Narasimhan, Madhumitha, et al. “Evolutionarily Unique Mechanistic Framework of Clathrin-Mediated Endocytosis in Plants.” ELife, vol. 9, e52067, eLife Sciences Publications, 2020, doi:10.7554/eLife.52067. short: M. Narasimhan, A.J. Johnson, R. Prizak, W. Kaufmann, S. Tan, B.E. Casillas Perez, J. Friml, ELife 9 (2020). date_created: 2020-02-16T23:00:50Z date_published: 2020-01-23T00:00:00Z date_updated: 2023-08-18T06:33:07Z day: '23' ddc: - '570' - '580' department: - _id: JiFr - _id: GaTk - _id: EM-Fac - _id: SyCr doi: 10.7554/eLife.52067 ec_funded: 1 external_id: isi: - '000514104100001' pmid: - '31971511' file: - access_level: open_access checksum: 2052daa4be5019534f3a42f200a09f32 content_type: application/pdf creator: dernst date_created: 2020-02-18T07:21:16Z date_updated: 2020-07-14T12:47:59Z file_id: '7494' file_name: 2020_eLife_Narasimhan.pdf file_size: 7247468 relation: main_file file_date_updated: 2020-07-14T12:47:59Z has_accepted_license: '1' intvolume: ' 9' isi: 1 language: - iso: eng month: '01' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: eLife publication_identifier: eissn: - 2050-084X publication_status: published publisher: eLife Sciences Publications quality_controlled: '1' scopus_import: '1' status: public title: Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 9 year: '2020' ... --- _id: '7497' abstract: - lang: eng text: Endophytic fungi can be beneficial to plant growth. However, the molecular mechanisms underlying colonization of Acremonium spp. remain unclear. In this study, a novel endophytic Acremonium strain was isolated from the buds of Panax notoginseng and named Acremonium sp. D212. The Acremonium sp. D212 could colonize the roots of P. notoginseng, enhance the resistance of P. notoginseng to root rot disease, and promote root growth and saponin biosynthesis in P. notoginseng. Acremonium sp. D212 could secrete indole‐3‐acetic acid (IAA) and jasmonic acid (JA), and inoculation with the fungus increased the endogenous levels of IAA and JA in P. notoginseng. Colonization of the Acremonium sp. D212 in the roots of the rice line Nipponbare was dependent on the concentration of methyl jasmonate (MeJA) (2 to 15 μM) and 1‐naphthalenacetic acid (NAA) (10 to 20 μM). Moreover, the roots of the JA signalling‐defective coi1‐18 mutant were colonized by Acremonium sp. D212 to a lesser degree than those of the wild‐type Nipponbare and miR393b‐overexpressing lines, and the colonization was rescued by MeJA but not by NAA. It suggests that the cross‐talk between JA signalling and the auxin biosynthetic pathway plays a crucial role in the colonization of Acremonium sp. D212 in host plants. acknowledgement: We thank Professor Jianqiang Wu (Kunming Institute of Botany, Chinese Academy of Sciences) for providing generous support with the IAA and JA measurements. We thank Professor Guohua Xu (Nanjing Agricultural University) for generously providing the Nipponbare rice expressing DR5::GUS. We thank Professor Muyuan Zhu (Zhejiang University) for generously providing a rice line expressing 35S::miR393b. We thank Professor Yinong Yang (Pennsylvania State University) for generously providing the rice line coi1-18. This work was supported by grants from the National Natural Science Foundation of China (31660501, 31460453, 31860064 and 31470382), the Major Special Program for Scientific Research, Education Department of Yunnan Province (ZD2015005), the Project sponsored by SRF for ROCS, SEM ([2013] 1792), the Major Science and Technique Programs in Yunnan Province (2016ZF001), the Key Projects of the Applied Basic Research Plan of Yunnan Province (2017FA018), the National Key R&D Program of China (2018YFD0201100) and the China Agriculture Research System (CARS-21). article_processing_charge: No article_type: original author: - first_name: L full_name: Han, L last_name: Han - first_name: X full_name: Zhou, X last_name: Zhou - first_name: Y full_name: Zhao, Y last_name: Zhao - first_name: S full_name: Zhu, S last_name: Zhu - first_name: L full_name: Wu, L last_name: Wu - first_name: Y full_name: He, Y last_name: He - first_name: X full_name: Ping, X last_name: Ping - first_name: X full_name: Lu, X last_name: Lu - first_name: W full_name: Huang, W last_name: Huang - first_name: J full_name: Qian, J last_name: Qian - first_name: L full_name: Zhang, L last_name: Zhang - first_name: X full_name: Jiang, X last_name: Jiang - first_name: D full_name: Zhu, D last_name: Zhu - first_name: C full_name: Luo, C last_name: Luo - first_name: S full_name: Li, S last_name: Li - first_name: Q full_name: Dong, Q last_name: Dong - first_name: Q full_name: Fu, Q last_name: Fu - first_name: K full_name: Deng, K last_name: Deng - first_name: X full_name: Wang, X last_name: Wang - first_name: L full_name: Wang, L last_name: Wang - first_name: S full_name: Peng, S last_name: Peng - first_name: J full_name: Wu, J last_name: Wu - first_name: W full_name: Li, W last_name: Li - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Y full_name: Zhu, Y last_name: Zhu - first_name: X full_name: He, X last_name: He - first_name: Y full_name: Du, Y last_name: Du citation: ama: Han L, Zhou X, Zhao Y, et al. Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid. Journal of Integrative Plant Biology. 2020;62(9):1433-1451. doi:10.1111/jipb.12905 apa: Han, L., Zhou, X., Zhao, Y., Zhu, S., Wu, L., He, Y., … Du, Y. (2020). Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid. Journal of Integrative Plant Biology. Wiley. https://doi.org/10.1111/jipb.12905 chicago: Han, L, X Zhou, Y Zhao, S Zhu, L Wu, Y He, X Ping, et al. “Colonization of Endophyte Acremonium Sp. D212 in Panax Notoginseng and Rice Mediated by Auxin and Jasmonic Acid.” Journal of Integrative Plant Biology. Wiley, 2020. https://doi.org/10.1111/jipb.12905. ieee: L. Han et al., “Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid,” Journal of Integrative Plant Biology, vol. 62, no. 9. Wiley, pp. 1433–1451, 2020. ista: Han L, Zhou X, Zhao Y, Zhu S, Wu L, He Y, Ping X, Lu X, Huang W, Qian J, Zhang L, Jiang X, Zhu D, Luo C, Li S, Dong Q, Fu Q, Deng K, Wang X, Wang L, Peng S, Wu J, Li W, Friml J, Zhu Y, He X, Du Y. 2020. Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid. Journal of Integrative Plant Biology. 62(9), 1433–1451. mla: Han, L., et al. “Colonization of Endophyte Acremonium Sp. D212 in Panax Notoginseng and Rice Mediated by Auxin and Jasmonic Acid.” Journal of Integrative Plant Biology, vol. 62, no. 9, Wiley, 2020, pp. 1433–51, doi:10.1111/jipb.12905. short: L. Han, X. Zhou, Y. Zhao, S. Zhu, L. Wu, Y. He, X. Ping, X. Lu, W. Huang, J. Qian, L. Zhang, X. Jiang, D. Zhu, C. Luo, S. Li, Q. Dong, Q. Fu, K. Deng, X. Wang, L. Wang, S. Peng, J. Wu, W. Li, J. Friml, Y. Zhu, X. He, Y. Du, Journal of Integrative Plant Biology 62 (2020) 1433–1451. date_created: 2020-02-18T10:02:25Z date_published: 2020-09-01T00:00:00Z date_updated: 2023-08-18T06:44:16Z day: '01' department: - _id: JiFr doi: 10.1111/jipb.12905 external_id: isi: - '000515803000001' pmid: - '31912615' intvolume: ' 62' isi: 1 issue: '9' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1111/jipb.12905 month: '09' oa: 1 oa_version: Published Version page: 1433-1451 pmid: 1 publication: Journal of Integrative Plant Biology publication_identifier: eissn: - 1744-7909 issn: - 1672-9072 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 62 year: '2020' ... --- _id: '7540' abstract: - lang: eng text: ' In vitro propagation of the ornamentally interesting species Wikstroemia gemmata is limited by the recalcitrance to form adventitious roots. In this article, two strategies to improve the rooting capacity of in vitro microcuttings are presented. Firstly, the effect of exogenous auxin was evaluated in both light and dark cultivated stem segments and also the sucrose-content of the medium was varied in order to determine better rooting conditions. Secondly, different spectral lights were evaluated and the effect on shoot growth and root induction demonstrated that the exact spectral composition of light is important for successful in vitro growth and development of Wikstroemia gemmata. We show that exogenous auxin cannot compensate for the poor rooting under unfavorable light conditions. Adapting the culture conditions is therefore paramount for successful industrial propagation of Wikstroemia gemmata. ' article_processing_charge: No article_type: original author: - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: H. full_name: Buyle, H. last_name: Buyle - first_name: S. full_name: Werbrouck, S. last_name: Werbrouck - first_name: M.C. full_name: Van Labeke, M.C. last_name: Van Labeke - first_name: D. full_name: Geelen, D. last_name: Geelen citation: ama: Verstraeten I, Buyle H, Werbrouck S, Van Labeke MC, Geelen D. In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality. Israel Journal of Plant Sciences. 2020;67(1-2):16-26. doi:10.1163/22238980-20191110 apa: Verstraeten, I., Buyle, H., Werbrouck, S., Van Labeke, M. C., & Geelen, D. (2020). In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality. Israel Journal of Plant Sciences. Brill. https://doi.org/10.1163/22238980-20191110 chicago: Verstraeten, Inge, H. Buyle, S. Werbrouck, M.C. Van Labeke, and D. Geelen. “In Vitro Shoot Growth and Adventitious Rooting of Wikstroemia Gemmata Depends on Light Quality.” Israel Journal of Plant Sciences. Brill, 2020. https://doi.org/10.1163/22238980-20191110. ieee: I. Verstraeten, H. Buyle, S. Werbrouck, M. C. Van Labeke, and D. Geelen, “In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality,” Israel Journal of Plant Sciences, vol. 67, no. 1–2. Brill, pp. 16–26, 2020. ista: Verstraeten I, Buyle H, Werbrouck S, Van Labeke MC, Geelen D. 2020. In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality. Israel Journal of Plant Sciences. 67(1–2), 16–26. mla: Verstraeten, Inge, et al. “In Vitro Shoot Growth and Adventitious Rooting of Wikstroemia Gemmata Depends on Light Quality.” Israel Journal of Plant Sciences, vol. 67, no. 1–2, Brill, 2020, pp. 16–26, doi:10.1163/22238980-20191110. short: I. Verstraeten, H. Buyle, S. Werbrouck, M.C. Van Labeke, D. Geelen, Israel Journal of Plant Sciences 67 (2020) 16–26. date_created: 2020-02-28T09:18:01Z date_published: 2020-02-01T00:00:00Z date_updated: 2023-08-18T06:45:15Z day: '01' department: - _id: JiFr doi: 10.1163/22238980-20191110 external_id: isi: - '000525343300004' intvolume: ' 67' isi: 1 issue: 1-2 language: - iso: eng month: '02' oa_version: None page: 16-26 publication: Israel Journal of Plant Sciences publication_identifier: eissn: - 2223-8980 issn: - 0792-9978 publication_status: published publisher: Brill quality_controlled: '1' scopus_import: '1' status: public title: In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 67 year: '2020' ... --- _id: '7582' abstract: - lang: eng text: Small RNAs (smRNA, 19–25 nucleotides long), which are transcribed by RNA polymerase II, regulate the expression of genes involved in a multitude of processes in eukaryotes. miRNA biogenesis and the proteins involved in the biogenesis pathway differ across plant and animal lineages. The major proteins constituting the biogenesis pathway, namely, the Dicers (DCL/DCR) and Argonautes (AGOs), have been extensively studied. However, the accessory proteins (DAWDLE (DDL), SERRATE (SE), and TOUGH (TGH)) of the pathway that differs across the two lineages remain largely uncharacterized. We present the first detailed report on the molecular evolution and divergence of these proteins across eukaryotes. Although DDL is present in eukaryotes and prokaryotes, SE and TGH appear to be specific to eukaryotes. The addition/deletion of specific domains and/or domain-specific sequence divergence in the three proteins points to the observed functional divergence of these proteins across the two lineages, which correlates with the differences in miRNA length across the two lineages. Our data enhance the current understanding of the structure–function relationship of these proteins and reveals previous unexplored crucial residues in the three proteins that can be used as a basis for further functional characterization. The data presented here on the number of miRNAs in crown eukaryotic lineages are consistent with the notion of the expansion of the number of miRNA-coding genes in animal and plant lineages correlating with organismal complexity. Whether this difference in functionally correlates with the diversification (or presence/absence) of the three proteins studied here or the miRNA signaling in the plant and animal lineages is unclear. Based on our results of the three proteins studied here and previously available data concerning the evolution of miRNA genes in the plant and animal lineages, we believe that miRNAs probably evolved once in the ancestor to crown eukaryotes and have diversified independently in the eukaryotes. article_number: '299' article_processing_charge: No article_type: original author: - first_name: Taraka Ramji full_name: Moturu, Taraka Ramji last_name: Moturu - first_name: Sansrity full_name: Sinha, Sansrity last_name: Sinha - first_name: Hymavathi full_name: Salava, Hymavathi last_name: Salava - first_name: Sravankumar full_name: Thula, Sravankumar last_name: Thula - first_name: Tomasz full_name: Nodzyński, Tomasz last_name: Nodzyński - first_name: Radka Svobodová full_name: Vařeková, Radka Svobodová last_name: Vařeková - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Sibu full_name: Simon, Sibu id: 4542EF9A-F248-11E8-B48F-1D18A9856A87 last_name: Simon orcid: 0000-0002-1998-6741 citation: ama: Moturu TR, Sinha S, Salava H, et al. Molecular evolution and diversification of proteins involved in miRNA maturation pathway. Plants. 2020;9(3). doi:10.3390/plants9030299 apa: Moturu, T. R., Sinha, S., Salava, H., Thula, S., Nodzyński, T., Vařeková, R. S., … Simon, S. (2020). Molecular evolution and diversification of proteins involved in miRNA maturation pathway. Plants. MDPI. https://doi.org/10.3390/plants9030299 chicago: Moturu, Taraka Ramji, Sansrity Sinha, Hymavathi Salava, Sravankumar Thula, Tomasz Nodzyński, Radka Svobodová Vařeková, Jiří Friml, and Sibu Simon. “Molecular Evolution and Diversification of Proteins Involved in MiRNA Maturation Pathway.” Plants. MDPI, 2020. https://doi.org/10.3390/plants9030299. ieee: T. R. Moturu et al., “Molecular evolution and diversification of proteins involved in miRNA maturation pathway,” Plants, vol. 9, no. 3. MDPI, 2020. ista: Moturu TR, Sinha S, Salava H, Thula S, Nodzyński T, Vařeková RS, Friml J, Simon S. 2020. Molecular evolution and diversification of proteins involved in miRNA maturation pathway. Plants. 9(3), 299. mla: Moturu, Taraka Ramji, et al. “Molecular Evolution and Diversification of Proteins Involved in MiRNA Maturation Pathway.” Plants, vol. 9, no. 3, 299, MDPI, 2020, doi:10.3390/plants9030299. short: T.R. Moturu, S. Sinha, H. Salava, S. Thula, T. Nodzyński, R.S. Vařeková, J. Friml, S. Simon, Plants 9 (2020). date_created: 2020-03-15T23:00:52Z date_published: 2020-03-01T00:00:00Z date_updated: 2023-08-18T07:07:08Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.3390/plants9030299 ec_funded: 1 external_id: isi: - '000525315000035' pmid: - '32121542' file: - access_level: open_access checksum: 6d5af3e17266a48996b4af4e67e88a85 content_type: application/pdf creator: dernst date_created: 2020-03-23T13:37:00Z date_updated: 2020-07-14T12:48:00Z file_id: '7614' file_name: 2020_Plants_Moturu.pdf file_size: 2373484 relation: main_file file_date_updated: 2020-07-14T12:48:00Z has_accepted_license: '1' intvolume: ' 9' isi: 1 issue: '3' language: - iso: eng month: '03' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: Plants publication_identifier: eissn: - '22237747' publication_status: published publisher: MDPI quality_controlled: '1' scopus_import: '1' status: public title: Molecular evolution and diversification of proteins involved in miRNA maturation pathway tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 9 year: '2020' ... --- _id: '7600' abstract: - lang: eng text: Directional intercellular transport of the phytohormone auxin mediated by PIN FORMED (PIN) efflux carriers plays essential roles in both coordinating patterning processes and integrating multiple external cues by rapidly redirecting auxin fluxes. Multilevel regulations of PIN activity under internal and external cues are complicated; however, the underlying molecular mechanism remains elusive. Here we demonstrate that 3’-Phosphoinositide-Dependent Protein Kinase1 (PDK1), which is conserved in plants and mammals, functions as a molecular hub integrating the upstream lipid signalling and the downstream substrate activity through phosphorylation. Genetic analysis uncovers that loss-of-function Arabidopsis mutant pdk1.1 pdk1.2 exhibits a plethora of abnormalities in organogenesis and growth, due to the defective PIN-dependent auxin transport. Further cellular and biochemical analyses reveal that PDK1 phosphorylates D6 Protein Kinase to facilitate its activity towards PIN proteins. Our studies establish a lipid-dependent phosphorylation cascade connecting membrane composition-based cellular signalling with plant growth and patterning by regulating morphogenetic auxin fluxes. acknowledged_ssus: - _id: Bio - _id: LifeSc article_processing_charge: No article_type: original author: - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Wei full_name: Kong, Wei last_name: Kong - first_name: Xiao-Li full_name: Yang, Xiao-Li last_name: Yang - first_name: Gergely full_name: Molnar, Gergely id: 34F1AF46-F248-11E8-B48F-1D18A9856A87 last_name: Molnar - first_name: Zuzana full_name: Vondráková, Zuzana last_name: Vondráková - first_name: Roberta full_name: Filepová, Roberta last_name: Filepová - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Hong-Wei full_name: Xue, Hong-Wei last_name: Xue citation: ama: Tan S, Zhang X, Kong W, et al. The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis. Nature Plants. 2020;6:556-569. doi:10.1038/s41477-020-0648-9 apa: Tan, S., Zhang, X., Kong, W., Yang, X.-L., Molnar, G., Vondráková, Z., … Xue, H.-W. (2020). The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis. Nature Plants. Springer Nature. https://doi.org/10.1038/s41477-020-0648-9 chicago: Tan, Shutang, Xixi Zhang, Wei Kong, Xiao-Li Yang, Gergely Molnar, Zuzana Vondráková, Roberta Filepová, Jan Petrášek, Jiří Friml, and Hong-Wei Xue. “The Lipid Code-Dependent Phosphoswitch PDK1–D6PK Activates PIN-Mediated Auxin Efflux in Arabidopsis.” Nature Plants. Springer Nature, 2020. https://doi.org/10.1038/s41477-020-0648-9. ieee: S. Tan et al., “The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis,” Nature Plants, vol. 6. Springer Nature, pp. 556–569, 2020. ista: Tan S, Zhang X, Kong W, Yang X-L, Molnar G, Vondráková Z, Filepová R, Petrášek J, Friml J, Xue H-W. 2020. The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis. Nature Plants. 6, 556–569. mla: Tan, Shutang, et al. “The Lipid Code-Dependent Phosphoswitch PDK1–D6PK Activates PIN-Mediated Auxin Efflux in Arabidopsis.” Nature Plants, vol. 6, Springer Nature, 2020, pp. 556–69, doi:10.1038/s41477-020-0648-9. short: S. Tan, X. Zhang, W. Kong, X.-L. Yang, G. Molnar, Z. Vondráková, R. Filepová, J. Petrášek, J. Friml, H.-W. Xue, Nature Plants 6 (2020) 556–569. date_created: 2020-03-21T16:34:16Z date_published: 2020-05-01T00:00:00Z date_updated: 2023-08-18T07:05:57Z day: '01' department: - _id: JiFr doi: 10.1038/s41477-020-0648-9 ec_funded: 1 external_id: isi: - '000531787500006' pmid: - '32393881' intvolume: ' 6' isi: 1 language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1101/755504 month: '05' oa: 1 oa_version: Preprint page: 556-569 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 256FEF10-B435-11E9-9278-68D0E5697425 grant_number: 723-2015 name: Long Term Fellowship publication: Nature Plants publication_identifier: eissn: - '20550278' publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: link: - relation: erratum url: https://doi.org/10.1038/s41477-020-0719-y scopus_import: '1' status: public title: The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 6 year: '2020' ... --- _id: '7646' abstract: - lang: eng text: In plant cells, environmental stressors promote changes in connectivity between the cortical ER and the PM. Although this process is tightly regulated in space and time, the molecular signals and structural components mediating these changes in inter-organelle communication are only starting to be characterized. In this report, we confirm the presence of a putative tethering complex containing the synaptotagmins 1 and 5 (SYT1 and SYT5) and the Ca2+ and lipid binding protein 1 (CLB1/SYT7). This complex is enriched at ER-PM contact sites (EPCS), have slow responses to changes in extracellular Ca2+, and display severe cytoskeleton-dependent rearrangements in response to the trivalent lanthanum (La3+) and gadolinium (Gd3+) rare earth elements (REEs). Although REEs are generally used as non-selective cation channel blockers at the PM, here we show that the slow internalization of REEs into the cytosol underlies the activation of the Ca2+/Calmodulin intracellular signaling, the accumulation of phosphatidylinositol-4-phosphate (PI4P) at the PM, and the cytoskeleton-dependent rearrangement of the SYT1/SYT5 EPCS complexes. We propose that the observed EPCS rearrangements act as a slow adaptive response to sustained stress conditions, and that this process involves the accumulation of stress-specific phosphoinositides species at the PM. article_processing_charge: No article_type: original author: - first_name: E full_name: Lee, E last_name: Lee - first_name: B full_name: Vila Nova Santana, B last_name: Vila Nova Santana - first_name: E full_name: Samuels, E last_name: Samuels - first_name: F full_name: Benitez-Fuente, F last_name: Benitez-Fuente - first_name: E full_name: Corsi, E last_name: Corsi - first_name: MA full_name: Botella, MA last_name: Botella - first_name: J full_name: Perez-Sancho, J last_name: Perez-Sancho - first_name: S full_name: Vanneste, S last_name: Vanneste - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: A full_name: Macho, A last_name: Macho - first_name: A full_name: Alves Azevedo, A last_name: Alves Azevedo - first_name: A full_name: Rosado, A last_name: Rosado citation: ama: Lee E, Vila Nova Santana B, Samuels E, et al. Rare earth elements induce cytoskeleton-dependent and PI4P-associated rearrangement of SYT1/SYT5 ER-PM contact site complexes in Arabidopsis. Journal of Experimental Botany. 2020;71(14):3986–3998. doi:10.1093/jxb/eraa138 apa: Lee, E., Vila Nova Santana, B., Samuels, E., Benitez-Fuente, F., Corsi, E., Botella, M., … Rosado, A. (2020). Rare earth elements induce cytoskeleton-dependent and PI4P-associated rearrangement of SYT1/SYT5 ER-PM contact site complexes in Arabidopsis. Journal of Experimental Botany. Oxford University Press. https://doi.org/10.1093/jxb/eraa138 chicago: Lee, E, B Vila Nova Santana, E Samuels, F Benitez-Fuente, E Corsi, MA Botella, J Perez-Sancho, et al. “Rare Earth Elements Induce Cytoskeleton-Dependent and PI4P-Associated Rearrangement of SYT1/SYT5 ER-PM Contact Site Complexes in Arabidopsis.” Journal of Experimental Botany. Oxford University Press, 2020. https://doi.org/10.1093/jxb/eraa138. ieee: E. Lee et al., “Rare earth elements induce cytoskeleton-dependent and PI4P-associated rearrangement of SYT1/SYT5 ER-PM contact site complexes in Arabidopsis,” Journal of Experimental Botany, vol. 71, no. 14. Oxford University Press, pp. 3986–3998, 2020. ista: Lee E, Vila Nova Santana B, Samuels E, Benitez-Fuente F, Corsi E, Botella M, Perez-Sancho J, Vanneste S, Friml J, Macho A, Alves Azevedo A, Rosado A. 2020. Rare earth elements induce cytoskeleton-dependent and PI4P-associated rearrangement of SYT1/SYT5 ER-PM contact site complexes in Arabidopsis. Journal of Experimental Botany. 71(14), 3986–3998. mla: Lee, E., et al. “Rare Earth Elements Induce Cytoskeleton-Dependent and PI4P-Associated Rearrangement of SYT1/SYT5 ER-PM Contact Site Complexes in Arabidopsis.” Journal of Experimental Botany, vol. 71, no. 14, Oxford University Press, 2020, pp. 3986–3998, doi:10.1093/jxb/eraa138. short: E. Lee, B. Vila Nova Santana, E. Samuels, F. Benitez-Fuente, E. Corsi, M. Botella, J. Perez-Sancho, S. Vanneste, J. Friml, A. Macho, A. Alves Azevedo, A. Rosado, Journal of Experimental Botany 71 (2020) 3986–3998. date_created: 2020-04-06T10:57:08Z date_published: 2020-07-06T00:00:00Z date_updated: 2023-08-18T10:27:52Z day: '06' ddc: - '580' department: - _id: JiFr doi: 10.1093/jxb/eraa138 external_id: isi: - '000553125400007' pmid: - '32179893' file: - access_level: open_access checksum: b06aaaa93dc41896da805fe4b75cf3a1 content_type: application/pdf creator: dernst date_created: 2020-10-06T07:41:35Z date_updated: 2020-10-06T07:41:35Z file_id: '8613' file_name: 2020_JourExperimBotany_Lee.pdf file_size: 1916031 relation: main_file success: 1 file_date_updated: 2020-10-06T07:41:35Z has_accepted_license: '1' intvolume: ' 71' isi: 1 issue: '14' language: - iso: eng month: '07' oa: 1 oa_version: Published Version page: 3986–3998 pmid: 1 publication: Journal of Experimental Botany publication_identifier: eissn: - 1460-2431 issn: - 0022-0957 publication_status: published publisher: Oxford University Press quality_controlled: '1' status: public title: Rare earth elements induce cytoskeleton-dependent and PI4P-associated rearrangement of SYT1/SYT5 ER-PM contact site complexes in Arabidopsis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 71 year: '2020' ... --- _id: '7686' abstract: - lang: eng text: 'The agricultural green revolution spectacularly enhanced crop yield and lodging resistance with modified DELLA-mediated gibberellin signaling. However, this was achieved at the expense of reduced nitrogen-use efficiency (NUE). Recently, Wu et al. revealed novel gibberellin signaling that provides a blueprint for improving tillering and NUE in Green Revolution varieties (GRVs). ' article_processing_charge: No article_type: original author: - first_name: Huidan full_name: Xue, Huidan last_name: Xue - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Guanghui full_name: Xiao, Guanghui last_name: Xiao citation: ama: 'Xue H, Zhang Y, Xiao G. Neo-gibberellin signaling: Guiding the next generation of the green revolution. Trends in Plant Science. 2020;25(6):520-522. doi:10.1016/j.tplants.2020.04.001' apa: 'Xue, H., Zhang, Y., & Xiao, G. (2020). Neo-gibberellin signaling: Guiding the next generation of the green revolution. Trends in Plant Science. Elsevier. https://doi.org/10.1016/j.tplants.2020.04.001' chicago: 'Xue, Huidan, Yuzhou Zhang, and Guanghui Xiao. “Neo-Gibberellin Signaling: Guiding the next Generation of the Green Revolution.” Trends in Plant Science. Elsevier, 2020. https://doi.org/10.1016/j.tplants.2020.04.001.' ieee: 'H. Xue, Y. Zhang, and G. Xiao, “Neo-gibberellin signaling: Guiding the next generation of the green revolution,” Trends in Plant Science, vol. 25, no. 6. Elsevier, pp. 520–522, 2020.' ista: 'Xue H, Zhang Y, Xiao G. 2020. Neo-gibberellin signaling: Guiding the next generation of the green revolution. Trends in Plant Science. 25(6), 520–522.' mla: 'Xue, Huidan, et al. “Neo-Gibberellin Signaling: Guiding the next Generation of the Green Revolution.” Trends in Plant Science, vol. 25, no. 6, Elsevier, 2020, pp. 520–22, doi:10.1016/j.tplants.2020.04.001.' short: H. Xue, Y. Zhang, G. Xiao, Trends in Plant Science 25 (2020) 520–522. date_created: 2020-04-26T22:00:46Z date_published: 2020-06-01T00:00:00Z date_updated: 2023-08-21T06:16:01Z day: '01' department: - _id: JiFr doi: 10.1016/j.tplants.2020.04.001 external_id: isi: - '000533518400003' pmid: - '32407691' intvolume: ' 25' isi: 1 issue: '6' language: - iso: eng month: '06' oa_version: None page: 520-522 pmid: 1 publication: Trends in Plant Science publication_identifier: issn: - 1360-1385 publication_status: published publisher: Elsevier quality_controlled: '1' scopus_import: '1' status: public title: 'Neo-gibberellin signaling: Guiding the next generation of the green revolution' type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 25 year: '2020' ... --- _id: '7793' abstract: - lang: eng text: Hormonal signalling in animals often involves direct transcription factor-hormone interactions that modulate gene expression. In contrast, plant hormone signalling is most commonly based on de-repression via the degradation of transcriptional repressors. Recently, we uncovered a non-canonical signalling mechanism for the plant hormone auxin whereby auxin directly affects the activity of the atypical auxin response factor (ARF), ETTIN towards target genes without the requirement for protein degradation. Here we show that ETTIN directly binds auxin, leading to dissociation from co-repressor proteins of the TOPLESS/TOPLESS-RELATED family followed by histone acetylation and induction of gene expression. This mechanism is reminiscent of animal hormone signalling as it affects the activity towards regulation of target genes and provides the first example of a DNA-bound hormone receptor in plants. Whilst auxin affects canonical ARFs indirectly by facilitating degradation of Aux/IAA repressors, direct ETTIN-auxin interactions allow switching between repressive and de-repressive chromatin states in an instantly-reversible manner. article_number: e51787 article_processing_charge: No article_type: original author: - first_name: André full_name: Kuhn, André last_name: Kuhn - first_name: Sigurd full_name: Ramans Harborough, Sigurd last_name: Ramans Harborough - first_name: Heather M full_name: McLaughlin, Heather M last_name: McLaughlin - first_name: Bhavani full_name: Natarajan, Bhavani last_name: Natarajan - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Stefan full_name: Kepinski, Stefan last_name: Kepinski - first_name: Lars full_name: Østergaard, Lars last_name: Østergaard citation: ama: Kuhn A, Ramans Harborough S, McLaughlin HM, et al. Direct ETTIN-auxin interaction controls chromatin states in gynoecium development. eLife. 2020;9. doi:10.7554/elife.51787 apa: Kuhn, A., Ramans Harborough, S., McLaughlin, H. M., Natarajan, B., Verstraeten, I., Friml, J., … Østergaard, L. (2020). Direct ETTIN-auxin interaction controls chromatin states in gynoecium development. ELife. eLife Sciences Publications. https://doi.org/10.7554/elife.51787 chicago: Kuhn, André, Sigurd Ramans Harborough, Heather M McLaughlin, Bhavani Natarajan, Inge Verstraeten, Jiří Friml, Stefan Kepinski, and Lars Østergaard. “Direct ETTIN-Auxin Interaction Controls Chromatin States in Gynoecium Development.” ELife. eLife Sciences Publications, 2020. https://doi.org/10.7554/elife.51787. ieee: A. Kuhn et al., “Direct ETTIN-auxin interaction controls chromatin states in gynoecium development,” eLife, vol. 9. eLife Sciences Publications, 2020. ista: Kuhn A, Ramans Harborough S, McLaughlin HM, Natarajan B, Verstraeten I, Friml J, Kepinski S, Østergaard L. 2020. Direct ETTIN-auxin interaction controls chromatin states in gynoecium development. eLife. 9, e51787. mla: Kuhn, André, et al. “Direct ETTIN-Auxin Interaction Controls Chromatin States in Gynoecium Development.” ELife, vol. 9, e51787, eLife Sciences Publications, 2020, doi:10.7554/elife.51787. short: A. Kuhn, S. Ramans Harborough, H.M. McLaughlin, B. Natarajan, I. Verstraeten, J. Friml, S. Kepinski, L. Østergaard, ELife 9 (2020). date_created: 2020-05-04T08:50:47Z date_published: 2020-04-08T00:00:00Z date_updated: 2023-08-21T06:17:12Z day: '08' ddc: - '580' department: - _id: JiFr doi: 10.7554/elife.51787 external_id: isi: - '000527752200001' pmid: - '32267233' file: - access_level: open_access checksum: 15d740de1a741fdcc6ec128c48eed017 content_type: application/pdf creator: dernst date_created: 2020-05-04T09:06:43Z date_updated: 2020-07-14T12:48:03Z file_id: '7794' file_name: 2020_eLife_Kuhn.pdf file_size: 2893082 relation: main_file file_date_updated: 2020-07-14T12:48:03Z has_accepted_license: '1' intvolume: ' 9' isi: 1 language: - iso: eng month: '04' oa: 1 oa_version: Published Version pmid: 1 publication: eLife publication_identifier: issn: - 2050-084X publication_status: published publisher: eLife Sciences Publications quality_controlled: '1' scopus_import: '1' status: public title: Direct ETTIN-auxin interaction controls chromatin states in gynoecium development tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 9 year: '2020' ... --- _id: '8138' abstract: - lang: eng text: Directional transport of the phytohormone auxin is a versatile, plant-specific mechanism regulating many aspects of plant development. The recently identified plant hormones, strigolactones (SLs), are implicated in many plant traits; among others, they modify the phenotypic output of PIN-FORMED (PIN) auxin transporters for fine-tuning of growth and developmental responses. Here, we show in pea and Arabidopsis that SLs target processes dependent on the canalization of auxin flow, which involves auxin feedback on PIN subcellular distribution. D14 receptor- and MAX2 F-box-mediated SL signaling inhibits the formation of auxin-conducting channels after wounding or from artificial auxin sources, during vasculature de novo formation and regeneration. At the cellular level, SLs interfere with auxin effects on PIN polar targeting, constitutive PIN trafficking as well as clathrin-mediated endocytosis. Our results identify a non-transcriptional mechanism of SL action, uncoupling auxin feedback on PIN polarity and trafficking, thereby regulating vascular tissue formation and regeneration. acknowledgement: We are grateful to David Nelson for providing published materials and extremely helpful comments, and Elizabeth Dun and Christine Beveridge for helpful discussions. The research leading to these results has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (742985). This work was also supported by the Beijing Municipal Natural Science Foundation (5192011), Beijing Outstanding University Discipline Program, the National Natural Science Foundation of China (31370309), CEITEC 2020 (LQ1601) project with financial contribution made by the Ministry of Education, Youth and Sports of the Czech Republic within special support paid from the National Program of Sustainability II funds, Australian Research Council (FT180100081), and China Postdoctoral Science Foundation (2019M660864). article_processing_charge: No article_type: original author: - first_name: J full_name: Zhang, J last_name: Zhang - first_name: E full_name: Mazur, E last_name: Mazur - first_name: J full_name: Balla, J last_name: Balla - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: P full_name: Kalousek, P last_name: Kalousek - first_name: Z full_name: Medveďová, Z last_name: Medveďová - first_name: Y full_name: Li, Y last_name: Li - first_name: Y full_name: Wang, Y last_name: Wang - first_name: Tomas full_name: Prat, Tomas id: 3DA3BFEE-F248-11E8-B48F-1D18A9856A87 last_name: Prat - first_name: Mina K full_name: Vasileva, Mina K id: 3407EB18-F248-11E8-B48F-1D18A9856A87 last_name: Vasileva - first_name: V full_name: Reinöhl, V last_name: Reinöhl - first_name: S full_name: Procházka, S last_name: Procházka - first_name: R full_name: Halouzka, R last_name: Halouzka - first_name: P full_name: Tarkowski, P last_name: Tarkowski - first_name: C full_name: Luschnig, C last_name: Luschnig - first_name: PB full_name: Brewer, PB last_name: Brewer - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang J, Mazur E, Balla J, et al. Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization. Nature Communications. 2020;11(1):3508. doi:10.1038/s41467-020-17252-y apa: Zhang, J., Mazur, E., Balla, J., Gallei, M. C., Kalousek, P., Medveďová, Z., … Friml, J. (2020). Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization. Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-020-17252-y chicago: Zhang, J, E Mazur, J Balla, Michelle C Gallei, P Kalousek, Z Medveďová, Y Li, et al. “Strigolactones Inhibit Auxin Feedback on PIN-Dependent Auxin Transport Canalization.” Nature Communications. Springer Nature, 2020. https://doi.org/10.1038/s41467-020-17252-y. ieee: J. Zhang et al., “Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization,” Nature Communications, vol. 11, no. 1. Springer Nature, p. 3508, 2020. ista: Zhang J, Mazur E, Balla J, Gallei MC, Kalousek P, Medveďová Z, Li Y, Wang Y, Prat T, Vasileva MK, Reinöhl V, Procházka S, Halouzka R, Tarkowski P, Luschnig C, Brewer P, Friml J. 2020. Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization. Nature Communications. 11(1), 3508. mla: Zhang, J., et al. “Strigolactones Inhibit Auxin Feedback on PIN-Dependent Auxin Transport Canalization.” Nature Communications, vol. 11, no. 1, Springer Nature, 2020, p. 3508, doi:10.1038/s41467-020-17252-y. short: J. Zhang, E. Mazur, J. Balla, M.C. Gallei, P. Kalousek, Z. Medveďová, Y. Li, Y. Wang, T. Prat, M.K. Vasileva, V. Reinöhl, S. Procházka, R. Halouzka, P. Tarkowski, C. Luschnig, P. Brewer, J. Friml, Nature Communications 11 (2020) 3508. date_created: 2020-07-21T08:58:07Z date_published: 2020-07-14T00:00:00Z date_updated: 2023-08-22T08:13:44Z day: '14' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41467-020-17252-y ec_funded: 1 external_id: isi: - '000550062200004' pmid: - '32665554' file: - access_level: open_access content_type: application/pdf creator: dernst date_created: 2020-07-22T08:32:55Z date_updated: 2020-07-22T08:32:55Z file_id: '8148' file_name: 2020_NatureComm_Zhang.pdf file_size: 1759490 relation: main_file success: 1 file_date_updated: 2020-07-22T08:32:55Z has_accepted_license: '1' intvolume: ' 11' isi: 1 issue: '1' language: - iso: eng month: '07' oa: 1 oa_version: Published Version page: '3508' pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Nature Communications publication_identifier: issn: - 2041-1723 publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: record: - id: '11626' relation: dissertation_contains status: public scopus_import: '1' status: public title: Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 11 year: '2020' ... --- _id: '8271' acknowledgement: We thank Dr. Gai Huang for his comments and help. We apologize to authors whose work could not be cited due to space limitation. No conflict of interest declared. article_processing_charge: No article_type: original author: - first_name: Peng full_name: He, Peng last_name: He - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Guanghui full_name: Xiao, Guanghui last_name: Xiao citation: ama: He P, Zhang Y, Xiao G. Origin of a subgenome and genome evolution of allotetraploid cotton species. Molecular Plant. 2020;13(9):1238-1240. doi:10.1016/j.molp.2020.07.006 apa: He, P., Zhang, Y., & Xiao, G. (2020). Origin of a subgenome and genome evolution of allotetraploid cotton species. Molecular Plant. Elsevier. https://doi.org/10.1016/j.molp.2020.07.006 chicago: He, Peng, Yuzhou Zhang, and Guanghui Xiao. “Origin of a Subgenome and Genome Evolution of Allotetraploid Cotton Species.” Molecular Plant. Elsevier, 2020. https://doi.org/10.1016/j.molp.2020.07.006. ieee: P. He, Y. Zhang, and G. Xiao, “Origin of a subgenome and genome evolution of allotetraploid cotton species,” Molecular Plant, vol. 13, no. 9. Elsevier, pp. 1238–1240, 2020. ista: He P, Zhang Y, Xiao G. 2020. Origin of a subgenome and genome evolution of allotetraploid cotton species. Molecular Plant. 13(9), 1238–1240. mla: He, Peng, et al. “Origin of a Subgenome and Genome Evolution of Allotetraploid Cotton Species.” Molecular Plant, vol. 13, no. 9, Elsevier, 2020, pp. 1238–40, doi:10.1016/j.molp.2020.07.006. short: P. He, Y. Zhang, G. Xiao, Molecular Plant 13 (2020) 1238–1240. date_created: 2020-08-16T22:00:57Z date_published: 2020-09-07T00:00:00Z date_updated: 2023-08-22T08:40:35Z day: '07' department: - _id: JiFr doi: 10.1016/j.molp.2020.07.006 external_id: isi: - '000566895400007' pmid: - '32688032' intvolume: ' 13' isi: 1 issue: '9' language: - iso: eng month: '09' oa_version: None page: 1238-1240 pmid: 1 publication: Molecular Plant publication_identifier: eissn: - '17529867' issn: - '16742052' publication_status: published publisher: Elsevier quality_controlled: '1' scopus_import: '1' status: public title: Origin of a subgenome and genome evolution of allotetraploid cotton species type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 13 year: '2020' ... --- _id: '8337' abstract: - lang: eng text: Cytokinins are mobile multifunctional plant hormones with roles in development and stress resilience. Although their Histidine Kinase receptors are substantially localised to the endoplasmic reticulum, cellular sites of cytokinin perception and importance of spatially heterogeneous cytokinin distribution continue to be debated. Here we show that cytokinin perception by plasma membrane receptors is an effective additional path for cytokinin response. Readout from a Two Component Signalling cytokinin-specific reporter (TCSn::GFP) closely matches intracellular cytokinin content in roots, yet we also find cytokinins in extracellular fluid, potentially enabling action at the cell surface. Cytokinins covalently linked to beads that could not pass the plasma membrane increased expression of both TCSn::GFP and Cytokinin Response Factors. Super-resolution microscopy of GFP-labelled receptors and diminished TCSn::GFP response to immobilised cytokinins in cytokinin receptor mutants, further indicate that receptors can function at the cell surface. We argue that dual intracellular and surface locations may augment flexibility of cytokinin responses. acknowledged_ssus: - _id: Bio acknowledgement: 'We thank Bruno Müller and Aaron Rashotte for critical discussions and provision of plant lines used in this work, Roger Granbom and Tamara Hernández Verdeja (UPSC, Umeå, Sweden) for technical assistance and providing materials, Zuzana Pěkná and Karolina Wojewodová (CRH, Palacký University, Olomouc, Czech Republic) for help with cytokinin receptor binding assays, and David Zalabák (CRH, Palacký University, Olomouc, Czech Republic) for provision of vector pINIIIΔEH expressing CRE1/AHK4. The bioimaging facility of IST Austria, the Swedish Metabolomics Centre and the IST Austria Bio-Imaging facility are acknowledged for support. The work was funded by the European Molecular Biology Organization (EMBO ASTF 297-2013) (I.A.), Development—The Company of Biologists (DEVTF2012) (I.A.; C.T.), Plant Fellows (the International Post doc Fellowship Programme in Plant Sciences, 267423) (I.A.; K.L.), the Swedish Research Council (621-2014-4514) (K.L.), UPSC Berzelii Center for Forest Biotechnology (Vinnova 2012-01560), Kempestiftelserna (JCK-2711) (K.L.) and (JCK-1811) (E.-M.B., K.L.). The Ministry of Education, Youth and Sports of the Czech Republic via the European Regional Development Fund-Project “Plants as a tool for sustainable global development” (CZ.02.1.01/0.0/0.0/16_019/0000827) (O.N., O.P., R.S., V.M., L.P., K.D.) and project CEITEC 2020 (LQ1601) (M.P., J.H.) provided support, as did the Czech Science Foundation via projects GP14-30004P (M.P.) and 16-04184S (O.P., K.D., O.N.), Vetenskapsrådet and Vinnova (Verket för Innovationssystem) (T.V., S.R.), Knut och Alice Wallenbergs Stiftelse via “Shapesystem” grant number 2012.0050. A.J. was supported by the Austria Science Fund (FWF): I03630 to J.F. The research leading to these results received funding from European Union’s Horizon 2020 programme (ERC grant no. 742985) and FWO-FWF joint project G0E5718N to J.F.' article_number: '4284' article_processing_charge: No article_type: original author: - first_name: Ioanna full_name: Antoniadi, Ioanna last_name: Antoniadi - first_name: Ondřej full_name: Novák, Ondřej last_name: Novák - first_name: Zuzana full_name: Gelová, Zuzana id: 0AE74790-0E0B-11E9-ABC7-1ACFE5697425 last_name: Gelová orcid: 0000-0003-4783-1752 - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Ondřej full_name: Plíhal, Ondřej last_name: Plíhal - first_name: Radim full_name: Simerský, Radim last_name: Simerský - first_name: Václav full_name: Mik, Václav last_name: Mik - first_name: Thomas full_name: Vain, Thomas last_name: Vain - first_name: Eduardo full_name: Mateo-Bonmatí, Eduardo last_name: Mateo-Bonmatí - first_name: Michal full_name: Karady, Michal last_name: Karady - first_name: Markéta full_name: Pernisová, Markéta last_name: Pernisová - first_name: Lenka full_name: Plačková, Lenka last_name: Plačková - first_name: Korawit full_name: Opassathian, Korawit last_name: Opassathian - first_name: Jan full_name: Hejátko, Jan last_name: Hejátko - first_name: Stéphanie full_name: Robert, Stéphanie last_name: Robert - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Karel full_name: Doležal, Karel last_name: Doležal - first_name: Karin full_name: Ljung, Karin last_name: Ljung - first_name: Colin full_name: Turnbull, Colin last_name: Turnbull citation: ama: Antoniadi I, Novák O, Gelová Z, et al. Cell-surface receptors enable perception of extracellular cytokinins. Nature Communications. 2020;11. doi:10.1038/s41467-020-17700-9 apa: Antoniadi, I., Novák, O., Gelová, Z., Johnson, A. J., Plíhal, O., Simerský, R., … Turnbull, C. (2020). Cell-surface receptors enable perception of extracellular cytokinins. Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-020-17700-9 chicago: Antoniadi, Ioanna, Ondřej Novák, Zuzana Gelová, Alexander J Johnson, Ondřej Plíhal, Radim Simerský, Václav Mik, et al. “Cell-Surface Receptors Enable Perception of Extracellular Cytokinins.” Nature Communications. Springer Nature, 2020. https://doi.org/10.1038/s41467-020-17700-9. ieee: I. Antoniadi et al., “Cell-surface receptors enable perception of extracellular cytokinins,” Nature Communications, vol. 11. Springer Nature, 2020. ista: Antoniadi I, Novák O, Gelová Z, Johnson AJ, Plíhal O, Simerský R, Mik V, Vain T, Mateo-Bonmatí E, Karady M, Pernisová M, Plačková L, Opassathian K, Hejátko J, Robert S, Friml J, Doležal K, Ljung K, Turnbull C. 2020. Cell-surface receptors enable perception of extracellular cytokinins. Nature Communications. 11, 4284. mla: Antoniadi, Ioanna, et al. “Cell-Surface Receptors Enable Perception of Extracellular Cytokinins.” Nature Communications, vol. 11, 4284, Springer Nature, 2020, doi:10.1038/s41467-020-17700-9. short: I. Antoniadi, O. Novák, Z. Gelová, A.J. Johnson, O. Plíhal, R. Simerský, V. Mik, T. Vain, E. Mateo-Bonmatí, M. Karady, M. Pernisová, L. Plačková, K. Opassathian, J. Hejátko, S. Robert, J. Friml, K. Doležal, K. Ljung, C. Turnbull, Nature Communications 11 (2020). date_created: 2020-09-06T22:01:13Z date_published: 2020-08-27T00:00:00Z date_updated: 2023-08-22T09:10:32Z day: '27' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41467-020-17700-9 ec_funded: 1 external_id: isi: - '000567931000001' file: - access_level: open_access checksum: 5b96f39b598de7510cfefefb819b9a6d content_type: application/pdf creator: dernst date_created: 2020-12-10T12:23:56Z date_updated: 2020-12-10T12:23:56Z file_id: '8936' file_name: 2020_NatureComm_Antoniadi.pdf file_size: 3526415 relation: main_file success: 1 file_date_updated: 2020-12-10T12:23:56Z has_accepted_license: '1' intvolume: ' 11' isi: 1 language: - iso: eng month: '08' oa: 1 oa_version: Published Version project: - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Nature Communications publication_identifier: eissn: - '20411723' publication_status: published publisher: Springer Nature quality_controlled: '1' scopus_import: '1' status: public title: Cell-surface receptors enable perception of extracellular cytokinins tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 11 year: '2020' ... --- _id: '8721' abstract: - lang: eng text: Spontaneously arising channels that transport the phytohormone auxin provide positional cues for self-organizing aspects of plant development such as flexible vasculature regeneration or its patterning during leaf venation. The auxin canalization hypothesis proposes a feedback between auxin signaling and transport as the underlying mechanism, but molecular players await discovery. We identified part of the machinery that routes auxin transport. The auxin-regulated receptor CAMEL (Canalization-related Auxin-regulated Malectin-type RLK) together with CANAR (Canalization-related Receptor-like kinase) interact with and phosphorylate PIN auxin transporters. camel and canar mutants are impaired in PIN1 subcellular trafficking and auxin-mediated PIN polarization, which macroscopically manifests as defects in leaf venation and vasculature regeneration after wounding. The CAMEL-CANAR receptor complex is part of the auxin feedback that coordinates polarization of individual cells during auxin canalization. acknowledged_ssus: - _id: Bio - _id: LifeSc acknowledgement: 'We acknowledge M. Glanc and Y. Zhang for providing entryclones; Vienna Biocenter Core Facilities (VBCF) for recombinantprotein production and purification; Vienna Biocenter Massspectrometry Facility, Bioimaging, and Life Science Facilities at IST Austria and Proteomics Core Facility CEITEC for a great assistance.Funding:This project received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (grant agreement 742985) and Austrian Science Fund (FWF): I 3630-B25 to J.F.and by grants from the Austrian Academy of Science through the Gregor Mendel Institute (Y.B.) and the Austrian Agency for International Cooperation in Education and Research (D.D.); the Netherlands Organization for Scientific Research (NWO; VIDI-864.13.001) (W.S.); the Research Foundation–Flanders (FWO;Odysseus II G0D0515N) and a European Research Council grant (ERC; StG TORPEDO; 714055) to B.D.R., B.Y., and E.M.; and the Hertha Firnberg Programme postdoctoral fellowship (T-947) from the FWF Austrian Science Fund to E.S.-L.; J.H. is the recipient of a DOC Fellowship of the Austrian Academy of Sciences at IST Austria.' article_processing_charge: No article_type: original author: - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Tomas full_name: Prat, Tomas id: 3DA3BFEE-F248-11E8-B48F-1D18A9856A87 last_name: Prat - first_name: N full_name: Rydza, N last_name: Rydza - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: David full_name: Domjan, David id: C684CD7A-257E-11EA-9B6F-D8588B4F947F last_name: Domjan orcid: 0000-0003-2267-106X - first_name: E full_name: Mazur, E last_name: Mazur - first_name: E full_name: Smakowska-Luzan, E last_name: Smakowska-Luzan - first_name: W full_name: Smet, W last_name: Smet - first_name: E full_name: Mor, E last_name: Mor - first_name: J full_name: Nolf, J last_name: Nolf - first_name: B full_name: Yang, B last_name: Yang - first_name: W full_name: Grunewald, W last_name: Grunewald - first_name: Gergely full_name: Molnar, Gergely id: 34F1AF46-F248-11E8-B48F-1D18A9856A87 last_name: Molnar - first_name: Y full_name: Belkhadir, Y last_name: Belkhadir - first_name: B full_name: De Rybel, B last_name: De Rybel - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Hajny J, Prat T, Rydza N, et al. Receptor kinase module targets PIN-dependent auxin transport during canalization. Science. 2020;370(6516):550-557. doi:10.1126/science.aba3178 apa: Hajny, J., Prat, T., Rydza, N., Rodriguez Solovey, L., Tan, S., Verstraeten, I., … Friml, J. (2020). Receptor kinase module targets PIN-dependent auxin transport during canalization. Science. American Association for the Advancement of Science. https://doi.org/10.1126/science.aba3178 chicago: Hajny, Jakub, Tomas Prat, N Rydza, Lesia Rodriguez Solovey, Shutang Tan, Inge Verstraeten, David Domjan, et al. “Receptor Kinase Module Targets PIN-Dependent Auxin Transport during Canalization.” Science. American Association for the Advancement of Science, 2020. https://doi.org/10.1126/science.aba3178. ieee: J. Hajny et al., “Receptor kinase module targets PIN-dependent auxin transport during canalization,” Science, vol. 370, no. 6516. American Association for the Advancement of Science, pp. 550–557, 2020. ista: Hajny J, Prat T, Rydza N, Rodriguez Solovey L, Tan S, Verstraeten I, Domjan D, Mazur E, Smakowska-Luzan E, Smet W, Mor E, Nolf J, Yang B, Grunewald W, Molnar G, Belkhadir Y, De Rybel B, Friml J. 2020. Receptor kinase module targets PIN-dependent auxin transport during canalization. Science. 370(6516), 550–557. mla: Hajny, Jakub, et al. “Receptor Kinase Module Targets PIN-Dependent Auxin Transport during Canalization.” Science, vol. 370, no. 6516, American Association for the Advancement of Science, 2020, pp. 550–57, doi:10.1126/science.aba3178. short: J. Hajny, T. Prat, N. Rydza, L. Rodriguez Solovey, S. Tan, I. Verstraeten, D. Domjan, E. Mazur, E. Smakowska-Luzan, W. Smet, E. Mor, J. Nolf, B. Yang, W. Grunewald, G. Molnar, Y. Belkhadir, B. De Rybel, J. Friml, Science 370 (2020) 550–557. date_created: 2020-11-02T10:04:46Z date_published: 2020-10-30T00:00:00Z date_updated: 2023-09-05T12:02:35Z day: '30' department: - _id: JiFr doi: 10.1126/science.aba3178 ec_funded: 1 external_id: isi: - '000583031800041' pmid: - '33122378' intvolume: ' 370' isi: 1 issue: '6516' language: - iso: eng main_file_link: - open_access: '1' url: https://europepmc.org/article/MED/33122378#free-full-text month: '10' oa: 1 oa_version: Published Version page: 550-557 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 2699E3D2-B435-11E9-9278-68D0E5697425 grant_number: '25239' name: Cell surface receptor complexes for PIN polarity and auxin-mediated development publication: Science publication_identifier: eissn: - 1095-9203 issn: - 0036-8075 publication_status: published publisher: American Association for the Advancement of Science quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/molecular-compass-for-cell-orientation/ scopus_import: '1' status: public title: Receptor kinase module targets PIN-dependent auxin transport during canalization type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 370 year: '2020' ... --- _id: '7949' abstract: - lang: eng text: Peptides derived from non-functional precursors play important roles in various developmental processes, but also in (a)biotic stress signaling. Our (phospho)proteome-wide analyses of C-terminally encoded peptide 5 (CEP5)-mediated changes revealed an impact on abiotic stress-related processes. Drought has a dramatic impact on plant growth, development and reproduction, and the plant hormone auxin plays a role in drought responses. Our genetic, physiological, biochemical and pharmacological results demonstrated that CEP5-mediated signaling is relevant for osmotic and drought stress tolerance in Arabidopsis, and that CEP5 specifically counteracts auxin effects. Specifically, we found that CEP5 signaling stabilizes AUX/IAA transcriptional repressors, suggesting the existence of a novel peptide-dependent control mechanism that tunes auxin signaling. These observations align with the recently described role of AUX/IAAs in stress tolerance and provide a novel role for CEP5 in osmotic and drought stress tolerance. acknowledgement: We thank Maria Njo, Sarah De Cokere, Marieke Mispelaere and Darren Wells, for practical assistance, Daniël Van Damme for assistance with image analysis, Marnik Vuylsteke for advice on statistics, Catherine Perrot-Rechenmann for useful discussions, Steffen Lau for critical reading oft he manuscript, and Philip Benfey, Gerd Jürgens, Philippe Nacry, Frederik Börnke, and Frans Tax for sharing materials. article_processing_charge: No article_type: original author: - first_name: S full_name: Smith, S last_name: Smith - first_name: S full_name: Zhu, S last_name: Zhu - first_name: L full_name: Joos, L last_name: Joos - first_name: I full_name: Roberts, I last_name: Roberts - first_name: N full_name: Nikonorova, N last_name: Nikonorova - first_name: LD full_name: Vu, LD last_name: Vu - first_name: E full_name: Stes, E last_name: Stes - first_name: H full_name: Cho, H last_name: Cho - first_name: A full_name: Larrieu, A last_name: Larrieu - first_name: W full_name: Xuan, W last_name: Xuan - first_name: B full_name: Goodall, B last_name: Goodall - first_name: B full_name: van de Cotte, B last_name: van de Cotte - first_name: JM full_name: Waite, JM last_name: Waite - first_name: A full_name: Rigal, A last_name: Rigal - first_name: SR full_name: R Harborough, SR last_name: R Harborough - first_name: G full_name: Persiau, G last_name: Persiau - first_name: S full_name: Vanneste, S last_name: Vanneste - first_name: GK full_name: Kirschner, GK last_name: Kirschner - first_name: E full_name: Vandermarliere, E last_name: Vandermarliere - first_name: L full_name: Martens, L last_name: Martens - first_name: Y full_name: Stahl, Y last_name: Stahl - first_name: D full_name: Audenaert, D last_name: Audenaert - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: G full_name: Felix, G last_name: Felix - first_name: R full_name: Simon, R last_name: Simon - first_name: M full_name: Bennett, M last_name: Bennett - first_name: A full_name: Bishopp, A last_name: Bishopp - first_name: G full_name: De Jaeger, G last_name: De Jaeger - first_name: K full_name: Ljung, K last_name: Ljung - first_name: S full_name: Kepinski, S last_name: Kepinski - first_name: S full_name: Robert, S last_name: Robert - first_name: J full_name: Nemhauser, J last_name: Nemhauser - first_name: I full_name: Hwang, I last_name: Hwang - first_name: K full_name: Gevaert, K last_name: Gevaert - first_name: T full_name: Beeckman, T last_name: Beeckman - first_name: I full_name: De Smet, I last_name: De Smet citation: ama: Smith S, Zhu S, Joos L, et al. The CEP5 peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis. Molecular & Cellular Proteomics. 2020;19(8):1248-1262. doi:10.1074/mcp.ra119.001826 apa: Smith, S., Zhu, S., Joos, L., Roberts, I., Nikonorova, N., Vu, L., … De Smet, I. (2020). The CEP5 peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis. Molecular & Cellular Proteomics. American Society for Biochemistry and Molecular Biology. https://doi.org/10.1074/mcp.ra119.001826 chicago: Smith, S, S Zhu, L Joos, I Roberts, N Nikonorova, LD Vu, E Stes, et al. “The CEP5 Peptide Promotes Abiotic Stress Tolerance, as Revealed by Quantitative Proteomics, and Attenuates the AUX/IAA Equilibrium in Arabidopsis.” Molecular & Cellular Proteomics. American Society for Biochemistry and Molecular Biology, 2020. https://doi.org/10.1074/mcp.ra119.001826. ieee: S. Smith et al., “The CEP5 peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis,” Molecular & Cellular Proteomics, vol. 19, no. 8. American Society for Biochemistry and Molecular Biology, pp. 1248–1262, 2020. ista: Smith S, Zhu S, Joos L, Roberts I, Nikonorova N, Vu L, Stes E, Cho H, Larrieu A, Xuan W, Goodall B, van de Cotte B, Waite J, Rigal A, R Harborough S, Persiau G, Vanneste S, Kirschner G, Vandermarliere E, Martens L, Stahl Y, Audenaert D, Friml J, Felix G, Simon R, Bennett M, Bishopp A, De Jaeger G, Ljung K, Kepinski S, Robert S, Nemhauser J, Hwang I, Gevaert K, Beeckman T, De Smet I. 2020. The CEP5 peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis. Molecular & Cellular Proteomics. 19(8), 1248–1262. mla: Smith, S., et al. “The CEP5 Peptide Promotes Abiotic Stress Tolerance, as Revealed by Quantitative Proteomics, and Attenuates the AUX/IAA Equilibrium in Arabidopsis.” Molecular & Cellular Proteomics, vol. 19, no. 8, American Society for Biochemistry and Molecular Biology, 2020, pp. 1248–62, doi:10.1074/mcp.ra119.001826. short: S. Smith, S. Zhu, L. Joos, I. Roberts, N. Nikonorova, L. Vu, E. Stes, H. Cho, A. Larrieu, W. Xuan, B. Goodall, B. van de Cotte, J. Waite, A. Rigal, S. R Harborough, G. Persiau, S. Vanneste, G. Kirschner, E. Vandermarliere, L. Martens, Y. Stahl, D. Audenaert, J. Friml, G. Felix, R. Simon, M. Bennett, A. Bishopp, G. De Jaeger, K. Ljung, S. Kepinski, S. Robert, J. Nemhauser, I. Hwang, K. Gevaert, T. Beeckman, I. De Smet, Molecular & Cellular Proteomics 19 (2020) 1248–1262. date_created: 2020-06-08T10:10:53Z date_published: 2020-08-01T00:00:00Z date_updated: 2023-09-05T12:17:46Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1074/mcp.ra119.001826 external_id: isi: - '000561114000001' pmid: - '32404488' file: - access_level: open_access checksum: 3f3f37b4a1ba2cfd270fc7733dd89680 content_type: application/pdf creator: kschuh date_created: 2021-05-05T10:10:14Z date_updated: 2021-05-05T10:10:14Z file_id: '9373' file_name: 2020_MCP_Smith.pdf file_size: 1632311 relation: main_file success: 1 file_date_updated: 2021-05-05T10:10:14Z has_accepted_license: '1' intvolume: ' 19' isi: 1 issue: '8' language: - iso: eng month: '08' oa: 1 oa_version: Published Version page: 1248-1262 pmid: 1 publication: Molecular & Cellular Proteomics publication_identifier: eissn: - 1535-9484 publication_status: published publisher: American Society for Biochemistry and Molecular Biology quality_controlled: '1' scopus_import: '1' status: public title: The CEP5 peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 19 year: '2020' ... --- _id: '7619' abstract: - lang: eng text: Cell polarity is a fundamental feature of all multicellular organisms. In plants, prominent cell polarity markers are PIN auxin transporters crucial for plant development. To identify novel components involved in cell polarity establishment and maintenance, we carried out a forward genetic screening with PIN2:PIN1-HA;pin2 Arabidopsis plants, which ectopically express predominantly basally localized PIN1 in the root epidermal cells leading to agravitropic root growth. From the screen, we identified the regulator of PIN polarity 12 (repp12) mutation, which restored gravitropic root growth and caused PIN1-HA polarity switch from basal to apical side of root epidermal cells. Complementation experiments established the repp12 causative mutation as an amino acid substitution in Aminophospholipid ATPase3 (ALA3), a phospholipid flippase with predicted function in vesicle formation. ala3 T-DNA mutants show defects in many auxin-regulated processes, in asymmetric auxin distribution and in PIN trafficking. Analysis of quintuple and sextuple mutants confirmed a crucial role of ALA proteins in regulating plant development and in PIN trafficking and polarity. Genetic and physical interaction studies revealed that ALA3 functions together with GNOM and BIG3 ARF GEFs. Taken together, our results identified ALA3 flippase as an important interactor and regulator of ARF GEF functioning in PIN polarity, trafficking and auxin-mediated development. acknowledged_ssus: - _id: Bio article_processing_charge: No article_type: original author: - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Petra full_name: Marhavá, Petra id: 44E59624-F248-11E8-B48F-1D18A9856A87 last_name: Marhavá - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Marta full_name: Zwiewka, Marta last_name: Zwiewka - first_name: Vendula full_name: Pukyšová, Vendula last_name: Pukyšová - first_name: Adrià Sans full_name: Sánchez, Adrià Sans last_name: Sánchez - first_name: Vivek Kumar full_name: Raxwal, Vivek Kumar last_name: Raxwal - first_name: Christian S. full_name: Hardtke, Christian S. last_name: Hardtke - first_name: Tomasz full_name: Nodzynski, Tomasz last_name: Nodzynski - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang X, Adamowski M, Marhavá P, et al. Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters. The Plant Cell. 2020;32(5):1644-1664. doi:10.1105/tpc.19.00869 apa: Zhang, X., Adamowski, M., Marhavá, P., Tan, S., Zhang, Y., Rodriguez Solovey, L., … Friml, J. (2020). Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters. The Plant Cell. American Society of Plant Biologists. https://doi.org/10.1105/tpc.19.00869 chicago: Zhang, Xixi, Maciek Adamowski, Petra Marhavá, Shutang Tan, Yuzhou Zhang, Lesia Rodriguez Solovey, Marta Zwiewka, et al. “Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters.” The Plant Cell. American Society of Plant Biologists, 2020. https://doi.org/10.1105/tpc.19.00869. ieee: X. Zhang et al., “Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters,” The Plant Cell, vol. 32, no. 5. American Society of Plant Biologists, pp. 1644–1664, 2020. ista: Zhang X, Adamowski M, Marhavá P, Tan S, Zhang Y, Rodriguez Solovey L, Zwiewka M, Pukyšová V, Sánchez AS, Raxwal VK, Hardtke CS, Nodzynski T, Friml J. 2020. Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters. The Plant Cell. 32(5), 1644–1664. mla: Zhang, Xixi, et al. “Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters.” The Plant Cell, vol. 32, no. 5, American Society of Plant Biologists, 2020, pp. 1644–64, doi:10.1105/tpc.19.00869. short: X. Zhang, M. Adamowski, P. Marhavá, S. Tan, Y. Zhang, L. Rodriguez Solovey, M. Zwiewka, V. Pukyšová, A.S. Sánchez, V.K. Raxwal, C.S. Hardtke, T. Nodzynski, J. Friml, The Plant Cell 32 (2020) 1644–1664. date_created: 2020-03-28T07:39:22Z date_published: 2020-05-01T00:00:00Z date_updated: 2023-09-05T12:21:06Z day: '01' department: - _id: JiFr doi: 10.1105/tpc.19.00869 ec_funded: 1 external_id: isi: - '000545741500030' pmid: - '32193204' intvolume: ' 32' isi: 1 issue: '5' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1105/tpc.19.00869 month: '05' oa: 1 oa_version: Published Version page: 1644-1664 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: The Plant Cell publication_identifier: eissn: - 1532-298X issn: - 1040-4651 publication_status: published publisher: American Society of Plant Biologists quality_controlled: '1' scopus_import: '1' status: public title: Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 32 year: '2020' ... --- _id: '8607' abstract: - lang: eng text: Clathrin-mediated endocytosis (CME) and its core endocytic machinery are evolutionarily conserved across all eukaryotes. In mammals, the heterotetrameric adaptor protein complex-2 (AP-2) sorts plasma membrane (PM) cargoes into vesicles through the recognition of motifs based on tyrosine or di-leucine in their cytoplasmic tails. However, in plants, very little is known on how PM proteins are sorted for CME and whether similar motifs are required. In Arabidopsis thaliana, the brassinosteroid (BR) receptor, BR INSENSITIVE1 (BRI1), undergoes endocytosis that depends on clathrin and AP-2. Here we demonstrate that BRI1 binds directly to the medium AP-2 subunit, AP2M. The cytoplasmic domain of BRI1 contains five putative canonical surface-exposed tyrosine-based endocytic motifs. The tyrosine-to-phenylalanine substitution in Y898KAI reduced BRI1 internalization without affecting its kinase activity. Consistently, plants carrying the BRI1Y898F mutation were hypersensitive to BRs. Our study demonstrates that AP-2-dependent internalization of PM proteins via the recognition of functional tyrosine motifs also operates in plants. article_processing_charge: No article_type: original author: - first_name: D full_name: Liu, D last_name: Liu - first_name: R full_name: Kumar, R last_name: Kumar - first_name: Claus full_name: LAN, Claus last_name: LAN - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: W full_name: Siao, W last_name: Siao - first_name: I full_name: Vanhoutte, I last_name: Vanhoutte - first_name: P full_name: Wang, P last_name: Wang - first_name: KW full_name: Bender, KW last_name: Bender - first_name: K full_name: Yperman, K last_name: Yperman - first_name: S full_name: Martins, S last_name: Martins - first_name: X full_name: Zhao, X last_name: Zhao - first_name: G full_name: Vert, G last_name: Vert - first_name: D full_name: Van Damme, D last_name: Van Damme - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: E full_name: Russinova, E last_name: Russinova citation: ama: Liu D, Kumar R, LAN C, et al. Endocytosis of BRASSINOSTEROID INSENSITIVE1 is partly driven by a canonical tyrosine-based Motif. Plant Cell. 2020;32(11):3598-3612. doi:10.1105/tpc.20.00384 apa: Liu, D., Kumar, R., LAN, C., Johnson, A. J., Siao, W., Vanhoutte, I., … Russinova, E. (2020). Endocytosis of BRASSINOSTEROID INSENSITIVE1 is partly driven by a canonical tyrosine-based Motif. Plant Cell. American Society of Plant Biologists. https://doi.org/10.1105/tpc.20.00384 chicago: Liu, D, R Kumar, Claus LAN, Alexander J Johnson, W Siao, I Vanhoutte, P Wang, et al. “Endocytosis of BRASSINOSTEROID INSENSITIVE1 Is Partly Driven by a Canonical Tyrosine-Based Motif.” Plant Cell. American Society of Plant Biologists, 2020. https://doi.org/10.1105/tpc.20.00384. ieee: D. Liu et al., “Endocytosis of BRASSINOSTEROID INSENSITIVE1 is partly driven by a canonical tyrosine-based Motif,” Plant Cell, vol. 32, no. 11. American Society of Plant Biologists, pp. 3598–3612, 2020. ista: Liu D, Kumar R, LAN C, Johnson AJ, Siao W, Vanhoutte I, Wang P, Bender K, Yperman K, Martins S, Zhao X, Vert G, Van Damme D, Friml J, Russinova E. 2020. Endocytosis of BRASSINOSTEROID INSENSITIVE1 is partly driven by a canonical tyrosine-based Motif. Plant Cell. 32(11), 3598–3612. mla: Liu, D., et al. “Endocytosis of BRASSINOSTEROID INSENSITIVE1 Is Partly Driven by a Canonical Tyrosine-Based Motif.” Plant Cell, vol. 32, no. 11, American Society of Plant Biologists, 2020, pp. 3598–612, doi:10.1105/tpc.20.00384. short: D. Liu, R. Kumar, C. LAN, A.J. Johnson, W. Siao, I. Vanhoutte, P. Wang, K. Bender, K. Yperman, S. Martins, X. Zhao, G. Vert, D. Van Damme, J. Friml, E. Russinova, Plant Cell 32 (2020) 3598–3612. date_created: 2020-10-05T12:45:16Z date_published: 2020-11-01T00:00:00Z date_updated: 2023-09-05T12:21:32Z day: '01' department: - _id: JiFr doi: 10.1105/tpc.20.00384 ec_funded: 1 external_id: isi: - '000600226800021' pmid: - '32958564' intvolume: ' 32' isi: 1 issue: '11' language: - iso: eng main_file_link: - open_access: '1' url: https://europepmc.org/article/MED/32958564 month: '11' oa: 1 oa_version: Published Version page: 3598-3612 pmid: 1 project: - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Plant Cell publication_identifier: eissn: - 1532-298x issn: - 1040-4651 publication_status: published publisher: American Society of Plant Biologists quality_controlled: '1' scopus_import: '1' status: public title: Endocytosis of BRASSINOSTEROID INSENSITIVE1 is partly driven by a canonical tyrosine-based Motif type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 32 year: '2020' ... --- _id: '7695' abstract: - lang: eng text: The TPLATE complex (TPC) is a key endocytic adaptor protein complex in plants. TPC in Arabidopsis (Arabidopsis thaliana) contains six evolutionarily conserved subunits and two plant-specific subunits, AtEH1/Pan1 and AtEH2/Pan1, although cytoplasmic proteins are not associated with the hexameric subcomplex in the cytoplasm. To investigate the dynamic assembly of the octameric TPC at the plasma membrane (PM), we performed state-of-the-art dual-color live cell imaging at physiological and lowered temperatures. Lowering the temperature slowed down endocytosis, thereby enhancing the temporal resolution of the differential recruitment of endocytic components. Under both normal and lowered temperature conditions, the core TPC subunit TPLATE and the AtEH/Pan1 proteins exhibited simultaneous recruitment at the PM. These results, together with co-localization analysis of different TPC subunits, allow us to conclude that TPC in plant cells is not recruited to the PM sequentially but as an octameric complex. article_processing_charge: No article_type: original author: - first_name: J full_name: Wang, J last_name: Wang - first_name: E full_name: Mylle, E last_name: Mylle - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: N full_name: Besbrugge, N last_name: Besbrugge - first_name: G full_name: De Jaeger, G last_name: De Jaeger - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: R full_name: Pleskot, R last_name: Pleskot - first_name: D full_name: van Damme, D last_name: van Damme citation: ama: Wang J, Mylle E, Johnson AJ, et al. High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits. Plant Physiology. 2020;183(3):986-997. doi:10.1104/pp.20.00178 apa: Wang, J., Mylle, E., Johnson, A. J., Besbrugge, N., De Jaeger, G., Friml, J., … van Damme, D. (2020). High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits. Plant Physiology. American Society of Plant Biologists. https://doi.org/10.1104/pp.20.00178 chicago: Wang, J, E Mylle, Alexander J Johnson, N Besbrugge, G De Jaeger, Jiří Friml, R Pleskot, and D van Damme. “High Temporal Resolution Reveals Simultaneous Plasma Membrane Recruitment of TPLATE Complex Subunits.” Plant Physiology. American Society of Plant Biologists, 2020. https://doi.org/10.1104/pp.20.00178. ieee: J. Wang et al., “High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits,” Plant Physiology, vol. 183, no. 3. American Society of Plant Biologists, pp. 986–997, 2020. ista: Wang J, Mylle E, Johnson AJ, Besbrugge N, De Jaeger G, Friml J, Pleskot R, van Damme D. 2020. High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits. Plant Physiology. 183(3), 986–997. mla: Wang, J., et al. “High Temporal Resolution Reveals Simultaneous Plasma Membrane Recruitment of TPLATE Complex Subunits.” Plant Physiology, vol. 183, no. 3, American Society of Plant Biologists, 2020, pp. 986–97, doi:10.1104/pp.20.00178. short: J. Wang, E. Mylle, A.J. Johnson, N. Besbrugge, G. De Jaeger, J. Friml, R. Pleskot, D. van Damme, Plant Physiology 183 (2020) 986–997. date_created: 2020-04-29T15:23:00Z date_published: 2020-07-01T00:00:00Z date_updated: 2023-09-05T12:20:02Z day: '01' department: - _id: JiFr doi: 10.1104/pp.20.00178 external_id: isi: - '000550682000018' pmid: - '32321842' intvolume: ' 183' isi: 1 issue: '3' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1101/2020.02.13.948109 month: '07' oa: 1 oa_version: Preprint page: 986-997 pmid: 1 project: - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: American Society of Plant Biologists quality_controlled: '1' scopus_import: '1' status: public title: High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 183 year: '2020' ... --- _id: '7697' abstract: - lang: eng text: "* Morphogenesis and adaptive tropic growth in plants depend on gradients of the phytohormone auxin, mediated by the membrane‐based PIN‐FORMED (PIN) auxin transporters. PINs localize to a particular side of the plasma membrane (PM) or to the endoplasmic reticulum (ER) to directionally transport auxin and maintain intercellular and intracellular auxin homeostasis, respectively. However, the molecular cues that confer their diverse cellular localizations remain largely unknown.\r\n* In this study, we systematically swapped the domains between ER‐ and PM‐localized PIN proteins, as well as between apical and basal PM‐localized PINs from Arabidopsis thaliana , to shed light on why PIN family members with similar topological structures reside at different membrane compartments within cells.\r\n* Our results show that not only do the N‐ and C‐terminal transmembrane domains (TMDs) and central hydrophilic loop contribute to their differential subcellular localizations and cellular polarity, but that the pairwise‐matched N‐ and C‐terminal TMDs resulting from intramolecular domain–domain coevolution are also crucial for their divergent patterns of localization.\r\n* These findings illustrate the complexity of the evolutionary path of PIN proteins in acquiring their plethora of developmental functions and adaptive growth in plants." article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Corinna full_name: Hartinger, Corinna id: AEFB2266-8ABF-11EA-AA39-812C3623CBE4 last_name: Hartinger orcid: 0000-0003-1618-2737 - first_name: Xiaojuan full_name: Wang, Xiaojuan last_name: Wang - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang Y, Hartinger C, Wang X, Friml J. Directional auxin fluxes in plants by intramolecular domain‐domain co‐evolution of PIN auxin transporters. New Phytologist. 2020;227(5):1406-1416. doi:10.1111/nph.16629 apa: Zhang, Y., Hartinger, C., Wang, X., & Friml, J. (2020). Directional auxin fluxes in plants by intramolecular domain‐domain co‐evolution of PIN auxin transporters. New Phytologist. Wiley. https://doi.org/10.1111/nph.16629 chicago: Zhang, Yuzhou, Corinna Hartinger, Xiaojuan Wang, and Jiří Friml. “Directional Auxin Fluxes in Plants by Intramolecular Domain‐domain Co‐evolution of PIN Auxin Transporters.” New Phytologist. Wiley, 2020. https://doi.org/10.1111/nph.16629. ieee: Y. Zhang, C. Hartinger, X. Wang, and J. Friml, “Directional auxin fluxes in plants by intramolecular domain‐domain co‐evolution of PIN auxin transporters,” New Phytologist, vol. 227, no. 5. Wiley, pp. 1406–1416, 2020. ista: Zhang Y, Hartinger C, Wang X, Friml J. 2020. Directional auxin fluxes in plants by intramolecular domain‐domain co‐evolution of PIN auxin transporters. New Phytologist. 227(5), 1406–1416. mla: Zhang, Yuzhou, et al. “Directional Auxin Fluxes in Plants by Intramolecular Domain‐domain Co‐evolution of PIN Auxin Transporters.” New Phytologist, vol. 227, no. 5, Wiley, 2020, pp. 1406–16, doi:10.1111/nph.16629. short: Y. Zhang, C. Hartinger, X. Wang, J. Friml, New Phytologist 227 (2020) 1406–1416. date_created: 2020-04-30T08:43:29Z date_published: 2020-09-01T00:00:00Z date_updated: 2023-09-05T15:46:04Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/nph.16629 ec_funded: 1 external_id: isi: - '000534092400001' pmid: - '32350870' file: - access_level: open_access checksum: 8e8150dbbba8cb65b72f81d1f0864b8b content_type: application/pdf creator: dernst date_created: 2020-11-24T12:19:38Z date_updated: 2020-11-24T12:19:38Z file_id: '8799' file_name: 2020_09_NewPhytologist_Zhang.pdf file_size: 3643395 relation: main_file success: 1 file_date_updated: 2020-11-24T12:19:38Z has_accepted_license: '1' intvolume: ' 227' isi: 1 issue: '5' language: - iso: eng month: '09' oa: 1 oa_version: Published Version page: 1406-1416 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646X publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Directional auxin fluxes in plants by intramolecular domain‐domain co‐evolution of PIN auxin transporters tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 227 year: '2020' ... --- _id: '7417' abstract: - lang: eng text: Previously, we reported that the allelic de-etiolated by zinc (dez) and trichome birefringence (tbr) mutants exhibit photomorphogenic development in the dark, which is enhanced by high Zn. TRICHOME BIREFRINGENCE-LIKE proteins had been implicated in transferring acetyl groups to various hemicelluloses. Pectin O-acetylation levels were lower in dark-grown dez seedlings than in the wild type. We observed Zn-enhanced photomorphogenesis in the dark also in the reduced wall acetylation 2 (rwa2-3) mutant, which exhibits lowered O-acetylation levels of cell wall macromolecules including pectins and xyloglucans, supporting a role for cell wall macromolecule O-acetylation in the photomorphogenic phenotypes of rwa2-3 and dez. Application of very short oligogalacturonides (vsOGs) restored skotomorphogenesis in dark-grown dez and rwa2-3. Here we demonstrate that in dez, O-acetylation of non-pectin cell wall components, notably of xyloglucan, is enhanced. Our results highlight the complexity of cell wall homeostasis and indicate against an influence of xyloglucan O-acetylation on light-dependent seedling development. article_number: e1687185 article_processing_charge: No article_type: original author: - first_name: Scott A full_name: Sinclair, Scott A id: 2D99FE6A-F248-11E8-B48F-1D18A9856A87 last_name: Sinclair orcid: 0000-0002-4566-0593 - first_name: S. full_name: Gille, S. last_name: Gille - first_name: M. full_name: Pauly, M. last_name: Pauly - first_name: U. full_name: Krämer, U. last_name: Krämer citation: ama: Sinclair SA, Gille S, Pauly M, Krämer U. Regulation of acetylation of plant cell wall components is complex and responds to external stimuli. Plant Signaling & Behavior. 2020;15(1). doi:10.1080/15592324.2019.1687185 apa: Sinclair, S. A., Gille, S., Pauly, M., & Krämer, U. (2020). Regulation of acetylation of plant cell wall components is complex and responds to external stimuli. Plant Signaling & Behavior. Informa UK Limited. https://doi.org/10.1080/15592324.2019.1687185 chicago: Sinclair, Scott A, S. Gille, M. Pauly, and U. Krämer. “Regulation of Acetylation of Plant Cell Wall Components Is Complex and Responds to External Stimuli.” Plant Signaling & Behavior. Informa UK Limited, 2020. https://doi.org/10.1080/15592324.2019.1687185. ieee: S. A. Sinclair, S. Gille, M. Pauly, and U. Krämer, “Regulation of acetylation of plant cell wall components is complex and responds to external stimuli,” Plant Signaling & Behavior, vol. 15, no. 1. Informa UK Limited, 2020. ista: Sinclair SA, Gille S, Pauly M, Krämer U. 2020. Regulation of acetylation of plant cell wall components is complex and responds to external stimuli. Plant Signaling & Behavior. 15(1), e1687185. mla: Sinclair, Scott A., et al. “Regulation of Acetylation of Plant Cell Wall Components Is Complex and Responds to External Stimuli.” Plant Signaling & Behavior, vol. 15, no. 1, e1687185, Informa UK Limited, 2020, doi:10.1080/15592324.2019.1687185. short: S.A. Sinclair, S. Gille, M. Pauly, U. Krämer, Plant Signaling & Behavior 15 (2020). date_created: 2020-01-30T10:14:14Z date_published: 2020-01-01T00:00:00Z date_updated: 2023-09-06T15:23:04Z day: '01' department: - _id: JiFr doi: 10.1080/15592324.2019.1687185 external_id: isi: - '000494907500001' pmid: - '31696770' intvolume: ' 15' isi: 1 issue: '1' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012154 month: '01' oa: 1 oa_version: Submitted Version pmid: 1 publication: Plant Signaling & Behavior publication_identifier: issn: - 1559-2324 publication_status: published publisher: Informa UK Limited quality_controlled: '1' scopus_import: '1' status: public title: Regulation of acetylation of plant cell wall components is complex and responds to external stimuli type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 15 year: '2020' ... --- _id: '8589' abstract: - lang: eng text: The plant hormone auxin plays indispensable roles in plant growth and development. An essential level of regulation in auxin action is the directional auxin transport within cells. The establishment of auxin gradient in plant tissue has been attributed to local auxin biosynthesis and directional intercellular auxin transport, which both are controlled by various environmental and developmental signals. It is well established that asymmetric auxin distribution in cells is achieved by polarly localized PIN-FORMED (PIN) auxin efflux transporters. Despite the initial insights into cellular mechanisms of PIN polarization obtained from the last decades, the molecular mechanism and specific regulators mediating PIN polarization remains elusive. In this thesis, we aim to find novel players in PIN subcellular polarity regulation during Arabidopsis development. We first characterize the physiological effect of piperonylic acid (PA) on Arabidopsis hypocotyl gravitropic bending and PIN polarization. Secondly, we reveal the importance of SCFTIR1/AFB auxin signaling pathway in shoot gravitropism bending termination. In addition, we also explore the role of myosin XI complex, and actin cytoskeleton in auxin feedback regulation on PIN polarity. In Chapter 1, we give an overview of the current knowledge about PIN-mediated auxin fluxes in various plant tropic responses. In Chapter 2, we study the physiological effect of PA on shoot gravitropic bending. Our results show that PA treatment inhibits auxin-mediated PIN3 repolarization by interfering with PINOID and PIN3 phosphorylation status, ultimately leading to hyperbending hypocotyls. In Chapter 3, we provide evidence to show that the SCFTIR1/AFB nuclear auxin signaling pathway is crucial and required for auxin-mediated PIN3 repolarization and shoot gravitropic bending termination. In Chapter 4, we perform a phosphoproteomics approach and identify the motor protein Myosin XI and its binding protein, the MadB2 family, as an essential regulator of PIN polarity for auxin-canalization related developmental processes. In Chapter 5, we demonstrate the vital role of actin cytoskeleton in auxin feedback on PIN polarity by regulating PIN subcellular trafficking. Overall, the data presented in this PhD thesis brings novel insights into the PIN polar localization regulation that resulted in the (re)establishment of the polar auxin flow and gradient in response to environmental stimuli during plant development. acknowledged_ssus: - _id: Bio - _id: LifeSc acknowledgement: I also want to thank the China Scholarship Council for supporting my study during the year from 2015 to 2019. I also want to thank IST facilities – the Bioimaging facility, the media kitchen, the plant facility and all of the campus services, for their support. alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han citation: ama: Han H. Novel insights into PIN polarity regulation during Arabidopsis development. 2020. doi:10.15479/AT:ISTA:8589 apa: Han, H. (2020). Novel insights into PIN polarity regulation during Arabidopsis development. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:8589 chicago: Han, Huibin. “Novel Insights into PIN Polarity Regulation during Arabidopsis Development.” Institute of Science and Technology Austria, 2020. https://doi.org/10.15479/AT:ISTA:8589. ieee: H. Han, “Novel insights into PIN polarity regulation during Arabidopsis development,” Institute of Science and Technology Austria, 2020. ista: Han H. 2020. Novel insights into PIN polarity regulation during Arabidopsis development. Institute of Science and Technology Austria. mla: Han, Huibin. Novel Insights into PIN Polarity Regulation during Arabidopsis Development. Institute of Science and Technology Austria, 2020, doi:10.15479/AT:ISTA:8589. short: H. Han, Novel Insights into PIN Polarity Regulation during Arabidopsis Development, Institute of Science and Technology Austria, 2020. date_created: 2020-09-30T14:50:51Z date_published: 2020-09-30T00:00:00Z date_updated: 2023-09-07T13:13:05Z day: '30' ddc: - '580' degree_awarded: PhD department: - _id: JiFr doi: 10.15479/AT:ISTA:8589 file: - access_level: closed checksum: c4bda1947d4c09c428ac9ce667b02327 content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: dernst date_created: 2020-09-30T14:50:20Z date_updated: 2020-09-30T14:50:20Z file_id: '8590' file_name: 2020_Han_Thesis.docx file_size: 49198118 relation: source_file - access_level: open_access checksum: 3f4f5d1718c2230adf30639ecaf8a00b content_type: application/pdf creator: dernst date_created: 2020-09-30T14:49:59Z date_updated: 2021-10-01T13:33:02Z file_id: '8591' file_name: 2020_Han_Thesis.pdf file_size: 15513963 relation: main_file file_date_updated: 2021-10-01T13:33:02Z has_accepted_license: '1' language: - iso: eng month: '09' oa: 1 oa_version: Published Version page: '164' publication_identifier: issn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '7643' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: Novel insights into PIN polarity regulation during Arabidopsis development type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2020' ... --- _id: '7643' acknowledgement: 'This work was supported by the European Research Council under the European Union’s Horizon 2020 research and innovation Programme (ERC grant agreement number 742985), and the Austrian Science Fund (FWF, grant number I 3630-B25) to JF. HH is supported by the China Scholarship Council (CSC scholarship). ' article_processing_charge: No article_type: letter_note author: - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: Hana full_name: Rakusova, Hana id: 4CAAA450-78D2-11EA-8E57-B40A396E08BA last_name: Rakusova - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Han H, Rakusova H, Verstraeten I, Zhang Y, Friml J. SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism. Plant Physiology. 2020;183(5):37-40. doi:10.1104/pp.20.00212 apa: Han, H., Rakusova, H., Verstraeten, I., Zhang, Y., & Friml, J. (2020). SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism. Plant Physiology. American Society of Plant Biologists. https://doi.org/10.1104/pp.20.00212 chicago: Han, Huibin, Hana Rakusova, Inge Verstraeten, Yuzhou Zhang, and Jiří Friml. “SCF TIR1/AFB Auxin Signaling for Bending Termination during Shoot Gravitropism.” Plant Physiology. American Society of Plant Biologists, 2020. https://doi.org/10.1104/pp.20.00212. ieee: H. Han, H. Rakusova, I. Verstraeten, Y. Zhang, and J. Friml, “SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism,” Plant Physiology, vol. 183, no. 5. American Society of Plant Biologists, pp. 37–40, 2020. ista: Han H, Rakusova H, Verstraeten I, Zhang Y, Friml J. 2020. SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism. Plant Physiology. 183(5), 37–40. mla: Han, Huibin, et al. “SCF TIR1/AFB Auxin Signaling for Bending Termination during Shoot Gravitropism.” Plant Physiology, vol. 183, no. 5, American Society of Plant Biologists, 2020, pp. 37–40, doi:10.1104/pp.20.00212. short: H. Han, H. Rakusova, I. Verstraeten, Y. Zhang, J. Friml, Plant Physiology 183 (2020) 37–40. date_created: 2020-04-06T10:06:40Z date_published: 2020-05-08T00:00:00Z date_updated: 2023-09-07T13:13:04Z day: '08' department: - _id: JiFr doi: 10.1104/pp.20.00212 ec_funded: 1 external_id: isi: - '000536641800018' pmid: - '32107280' intvolume: ' 183' isi: 1 issue: '5' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1104/pp.20.00212 month: '05' oa: 1 oa_version: Published Version page: 37-40 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: American Society of Plant Biologists quality_controlled: '1' related_material: record: - id: '8589' relation: dissertation_contains status: public scopus_import: '1' status: public title: SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 183 year: '2020' ... --- _id: '7416' abstract: - lang: eng text: Earlier, we demonstrated that transcript levels of METAL TOLERANCE PROTEIN2 (MTP2) and of HEAVY METAL ATPase2 (HMA2) increase strongly in roots of Arabidopsis upon prolonged zinc (Zn) deficiency and respond to shoot physiological Zn status, and not to the local Zn status in roots. This provided evidence for shoot-to-root communication in the acclimation of plants to Zn deficiency. Zn-deficient soils limit both the yield and quality of agricultural crops and can result in clinically relevant nutritional Zn deficiency in human populations. Implementing Zn deficiency during cultivation of the model plant Arabidopsis thaliana on agar-solidified media is difficult because trace element contaminations are present in almost all commercially available agars. Here, we demonstrate root morphological acclimations to Zn deficiency on agar-solidified medium following the effective removal of contaminants. These advancements allow reproducible phenotyping toward understanding fundamental plant responses to deficiencies of Zn and other essential trace elements. article_number: '1687175' article_processing_charge: No article_type: original author: - first_name: Scott A full_name: Sinclair, Scott A id: 2D99FE6A-F248-11E8-B48F-1D18A9856A87 last_name: Sinclair orcid: 0000-0002-4566-0593 - first_name: U. full_name: Krämer, U. last_name: Krämer citation: ama: Sinclair SA, Krämer U. Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation. Plant Signaling & Behavior. 2020;15(1). doi:10.1080/15592324.2019.1687175 apa: Sinclair, S. A., & Krämer, U. (2020). Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation. Plant Signaling & Behavior. Taylor & Francis. https://doi.org/10.1080/15592324.2019.1687175 chicago: Sinclair, Scott A, and U. Krämer. “Generation of Effective Zinc-Deficient Agar-Solidified Media Allows Identification of Root Morphology Changes in Response to Zinc Limitation.” Plant Signaling & Behavior. Taylor & Francis, 2020. https://doi.org/10.1080/15592324.2019.1687175. ieee: S. A. Sinclair and U. Krämer, “Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation,” Plant Signaling & Behavior, vol. 15, no. 1. Taylor & Francis, 2020. ista: Sinclair SA, Krämer U. 2020. Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation. Plant Signaling & Behavior. 15(1), 1687175. mla: Sinclair, Scott A., and U. Krämer. “Generation of Effective Zinc-Deficient Agar-Solidified Media Allows Identification of Root Morphology Changes in Response to Zinc Limitation.” Plant Signaling & Behavior, vol. 15, no. 1, 1687175, Taylor & Francis, 2020, doi:10.1080/15592324.2019.1687175. short: S.A. Sinclair, U. Krämer, Plant Signaling & Behavior 15 (2020). date_created: 2020-01-30T10:12:04Z date_published: 2020-01-01T00:00:00Z date_updated: 2023-10-17T09:01:48Z day: '01' department: - _id: JiFr doi: 10.1080/15592324.2019.1687175 external_id: isi: - '000494909300001' pmid: - '31696764' intvolume: ' 15' isi: 1 issue: '1' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012054 month: '01' oa: 1 oa_version: Submitted Version pmid: 1 publication: Plant Signaling & Behavior publication_identifier: issn: - 1559-2324 publication_status: published publisher: Taylor & Francis quality_controlled: '1' scopus_import: '1' status: public title: Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 15 year: '2020' ... --- _id: '8943' abstract: - lang: eng text: The widely used non-steroidal anti-inflammatory drugs (NSAIDs) are derivatives of the phytohormone salicylic acid (SA). SA is well known to regulate plant immunity and development, whereas there have been few reports focusing on the effects of NSAIDs in plants. Our studies here reveal that NSAIDs exhibit largely overlapping physiological activities to SA in the model plant Arabidopsis. NSAID treatments lead to shorter and agravitropic primary roots and inhibited lateral root organogenesis. Notably, in addition to the SA-like action, which in roots involves binding to the protein phosphatase 2A (PP2A), NSAIDs also exhibit PP2A-independent effects. Cell biological and biochemical analyses reveal that many NSAIDs bind directly to and inhibit the chaperone activity of TWISTED DWARF1, thereby regulating actin cytoskeleton dynamics and subsequent endosomal trafficking. Our findings uncover an unexpected bioactivity of human pharmaceuticals in plants and provide insights into the molecular mechanism underlying the cellular action of this class of anti-inflammatory compounds. acknowledged_ssus: - _id: LifeSc - _id: Bio acknowledgement: "We thank Drs. Sebastian Bednarek (University of Wisconsin-Madison), Niko Geldner (University of Lausanne), and Karin Schumacher (Heidelberg University) for kindly sharing published Arabidopsis lines; Dr. Satoshi Naramoto for the pPIN2::PIN2-GFP; pVHA-a1::VHA-a1-mRFP reporter; the staff at the Life Science Facility and Bioimaging Facility, Monika Hrtyan, and Dorota Jaworska at IST Austria for technical support; and Drs. Su Tang (Texas A&M University),\r\nMelinda Abas (BOKU), Eva Benkova´ (IST Austria), Christian Luschnig (BOKU), Bartel Vanholme (Gent University), and the Friml group for valuable discussions. The research leading to these findings was funded by the European Union’s Horizon 2020 program (ERC grant agreement no. 742985, to J.F.), the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme (FP7/2007-2013) under REA grant agreement no.\r\n291734, the Swiss National Funds (31003A_165877, to M.G.), the Ministry of Education, Youth, and Sports of the Czech Republic (project no. CZ.02.1.01/0.0/0.0/16_019/0000738, EU Operational Programme ‘‘Research, development and education and Centre for Plant Experimental Biology’’), and the EU Operational Programme Prague - Competitiveness (project no. CZ.2.16/3.1.00/21519). S.T. was funded by a European Molecular Biology Organization (EMBO) long-term postdoctoral fellowship (ALTF 723-2015). X.Z. was partly supported by a PhD scholarship from the China Scholarship Council." article_number: '108463' article_processing_charge: Yes article_type: original author: - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Martin full_name: Di Donato, Martin last_name: Di Donato - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Petr full_name: Klíma, Petr last_name: Klíma - first_name: Jie full_name: Liu, Jie last_name: Liu - first_name: Aurélien full_name: Bailly, Aurélien last_name: Bailly - first_name: Noel full_name: Ferro, Noel last_name: Ferro - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Markus full_name: Geisler, Markus last_name: Geisler - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Tan S, Di Donato M, Glanc M, et al. Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development. Cell Reports. 2020;33(9). doi:10.1016/j.celrep.2020.108463 apa: Tan, S., Di Donato, M., Glanc, M., Zhang, X., Klíma, P., Liu, J., … Friml, J. (2020). Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development. Cell Reports. Elsevier. https://doi.org/10.1016/j.celrep.2020.108463 chicago: Tan, Shutang, Martin Di Donato, Matous Glanc, Xixi Zhang, Petr Klíma, Jie Liu, Aurélien Bailly, et al. “Non-Steroidal Anti-Inflammatory Drugs Target TWISTED DWARF1-Regulated Actin Dynamics and Auxin Transport-Mediated Plant Development.” Cell Reports. Elsevier, 2020. https://doi.org/10.1016/j.celrep.2020.108463. ieee: S. Tan et al., “Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development,” Cell Reports, vol. 33, no. 9. Elsevier, 2020. ista: Tan S, Di Donato M, Glanc M, Zhang X, Klíma P, Liu J, Bailly A, Ferro N, Petrášek J, Geisler M, Friml J. 2020. Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development. Cell Reports. 33(9), 108463. mla: Tan, Shutang, et al. “Non-Steroidal Anti-Inflammatory Drugs Target TWISTED DWARF1-Regulated Actin Dynamics and Auxin Transport-Mediated Plant Development.” Cell Reports, vol. 33, no. 9, 108463, Elsevier, 2020, doi:10.1016/j.celrep.2020.108463. short: S. Tan, M. Di Donato, M. Glanc, X. Zhang, P. Klíma, J. Liu, A. Bailly, N. Ferro, J. Petrášek, M. Geisler, J. Friml, Cell Reports 33 (2020). date_created: 2020-12-13T23:01:21Z date_published: 2020-12-01T00:00:00Z date_updated: 2023-11-16T13:03:31Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1016/j.celrep.2020.108463 ec_funded: 1 external_id: isi: - '000595658100018' pmid: - '33264621' file: - access_level: open_access checksum: ed18cba0fb48ed2e789381a54cc21904 content_type: application/pdf creator: dernst date_created: 2020-12-14T07:33:39Z date_updated: 2020-12-14T07:33:39Z file_id: '8948' file_name: 2020_CellReports_Tan.pdf file_size: 8056434 relation: main_file success: 1 file_date_updated: 2020-12-14T07:33:39Z has_accepted_license: '1' intvolume: ' 33' isi: 1 issue: '9' language: - iso: eng month: '12' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme - _id: 256FEF10-B435-11E9-9278-68D0E5697425 grant_number: 723-2015 name: Long Term Fellowship publication: Cell Reports publication_identifier: eissn: - '22111247' publication_status: published publisher: Elsevier quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/plants-on-aspirin/ scopus_import: '1' status: public title: Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87 volume: 33 year: '2020' ... --- _id: '8002' abstract: - lang: eng text: Wound healing in plant tissues, consisting of rigid cell wall-encapsulated cells, represents a considerable challenge and occurs through largely unknown mechanisms distinct from those in animals. Owing to their inability to migrate, plant cells rely on targeted cell division and expansion to regenerate wounds. Strict coordination of these wound-induced responses is essential to ensure efficient, spatially restricted wound healing. Single-cell tracking by live imaging allowed us to gain mechanistic insight into the wound perception and coordination of wound responses after laser-based wounding in Arabidopsis root. We revealed a crucial contribution of the collapse of damaged cells in wound perception and detected an auxin increase specific to cells immediately adjacent to the wound. This localized auxin increase balances wound-induced cell expansion and restorative division rates in a dose-dependent manner, leading to tumorous overproliferation when the canonical TIR1 auxin signaling is disrupted. Auxin and wound-induced turgor pressure changes together also spatially define the activation of key components of regeneration, such as the transcription regulator ERF115. Our observations suggest that the wound signaling involves the sensing of collapse of damaged cells and a local auxin signaling activation to coordinate the downstream transcriptional responses in the immediate wound vicinity. acknowledged_ssus: - _id: Bio - _id: LifeSc article_number: '202003346' article_processing_charge: No article_type: original author: - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 - first_name: Juan C full_name: Montesinos López, Juan C id: 310A8E3E-F248-11E8-B48F-1D18A9856A87 last_name: Montesinos López orcid: 0000-0001-9179-6099 - first_name: Petra full_name: Marhavá, Petra id: 44E59624-F248-11E8-B48F-1D18A9856A87 last_name: Marhavá - first_name: Eva full_name: Benková, Eva id: 38F4F166-F248-11E8-B48F-1D18A9856A87 last_name: Benková orcid: 0000-0002-8510-9739 - first_name: Saiko full_name: Yoshida, Saiko id: 2E46069C-F248-11E8-B48F-1D18A9856A87 last_name: Yoshida - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Hörmayer L, Montesinos López JC, Marhavá P, Benková E, Yoshida S, Friml J. Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots. Proceedings of the National Academy of Sciences. 2020;117(26). doi:10.1073/pnas.2003346117 apa: Hörmayer, L., Montesinos López, J. C., Marhavá, P., Benková, E., Yoshida, S., & Friml, J. (2020). Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.2003346117 chicago: Hörmayer, Lukas, Juan C Montesinos López, Petra Marhavá, Eva Benková, Saiko Yoshida, and Jiří Friml. “Wounding-Induced Changes in Cellular Pressure and Localized Auxin Signalling Spatially Coordinate Restorative Divisions in Roots.” Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences, 2020. https://doi.org/10.1073/pnas.2003346117. ieee: L. Hörmayer, J. C. Montesinos López, P. Marhavá, E. Benková, S. Yoshida, and J. Friml, “Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots,” Proceedings of the National Academy of Sciences, vol. 117, no. 26. Proceedings of the National Academy of Sciences, 2020. ista: Hörmayer L, Montesinos López JC, Marhavá P, Benková E, Yoshida S, Friml J. 2020. Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots. Proceedings of the National Academy of Sciences. 117(26), 202003346. mla: Hörmayer, Lukas, et al. “Wounding-Induced Changes in Cellular Pressure and Localized Auxin Signalling Spatially Coordinate Restorative Divisions in Roots.” Proceedings of the National Academy of Sciences, vol. 117, no. 26, 202003346, Proceedings of the National Academy of Sciences, 2020, doi:10.1073/pnas.2003346117. short: L. Hörmayer, J.C. Montesinos López, P. Marhavá, E. Benková, S. Yoshida, J. Friml, Proceedings of the National Academy of Sciences 117 (2020). date_created: 2020-06-22T13:33:52Z date_published: 2020-06-30T00:00:00Z date_updated: 2024-03-27T23:30:11Z day: '30' ddc: - '580' department: - _id: JiFr - _id: EvBe doi: 10.1073/pnas.2003346117 ec_funded: 1 external_id: isi: - '000565729700033' pmid: - '32541049' file: - access_level: open_access checksum: 908b09437680181de9990915f2113aca content_type: application/pdf creator: dernst date_created: 2020-06-23T11:30:53Z date_updated: 2020-07-14T12:48:07Z file_id: '8009' file_name: 2020_PNAS_Hoermayer.pdf file_size: 2407102 relation: main_file file_date_updated: 2020-07-14T12:48:07Z has_accepted_license: '1' intvolume: ' 117' isi: 1 issue: '26' language: - iso: eng month: '06' oa: 1 oa_version: None pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 262EF96E-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: P29988 name: RNA-directed DNA methylation in plant development publication: Proceedings of the National Academy of Sciences publication_identifier: eissn: - 1091-6490 issn: - 0027-8424 publication_status: published publisher: Proceedings of the National Academy of Sciences quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/how-wounded-plants-coordinate-their-healing/ record: - id: '9992' relation: dissertation_contains status: public scopus_import: '1' status: public title: Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 117 year: '2020' ... --- _id: '7427' abstract: - lang: eng text: Plants, like other multicellular organisms, survive through a delicate balance between growth and defense against pathogens. Salicylic acid (SA) is a major defense signal in plants, and the perception mechanism as well as downstream signaling activating the immune response are known. Here, we identify a parallel SA signaling that mediates growth attenuation. SA directly binds to A subunits of protein phosphatase 2A (PP2A), inhibiting activity of this complex. Among PP2A targets, the PIN2 auxin transporter is hyperphosphorylated in response to SA, leading to changed activity of this important growth regulator. Accordingly, auxin transport and auxin-mediated root development, including growth, gravitropic response, and lateral root organogenesis, are inhibited. This study reveals how SA, besides activating immunity, concomitantly attenuates growth through crosstalk with the auxin distribution network. Further analysis of this dual role of SA and characterization of additional SA-regulated PP2A targets will provide further insights into mechanisms maintaining a balance between growth and defense. acknowledged_ssus: - _id: Bio - _id: LifeSc acknowledgement: "We thank Shigeyuki Betsuyaku (University of Tsukuba), Alison Delong (Brown University), Xinnian Dong (Duke University), Dolf Weijers (Wageningen University), Yuelin Zhang (UBC), and Martine Pastuglia (Institut Jean-Pierre Bourgin) for sharing published materials; Jana Riederer for help with cantharidin physiological analysis; David Domjan for help with cloning pET28a-PIN2HL; Qing Lu for help with DARTS; Hana Kozubı´kova´ for technical support on SA derivative synthesis; Zuzana Vondra´ kova´ for technical support with tobacco cells; Lucia Strader (Washington University), Bert De Rybel (Ghent University), Bartel Vanholme (Ghent University), and Lukas Mach (BOKU) for helpful discussions; and bioimaging and life science facilities of IST Austria for continuous support. We gratefully acknowledge the Nottingham Arabidopsis Stock Center (NASC) for providing T-DNA insertional mutants. The DSC and SPR instruments were provided by the EQ-BOKU VIBT GmbH and the BOKU Core Facility for Biomolecular and Cellular Analysis, with help of Irene Schaffner. The research leading to these results has received funding from the European Union’s Horizon 2020 program (ERC grant agreement no. 742985 to J.F.) and the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme (FP7/2007-2013) under REA grant agreement no. 291734. S.T. was supported by a European Molecular Biology Organization (EMBO) long-term postdoctoral fellowship (ALTF 723-2015). O.N. was supported by the Ministry of Education, Youth and Sports of the Czech Republic (European Regional Development Fund-Project ‘‘Centre for Experimental Plant Biology’’ no. CZ.02.1.01/0.0/0.0/16_019/0000738). J. Pospısil was supported by European Regional Development Fund Project ‘‘Centre for Experimental Plant Biology’’\r\n(no. CZ.02.1.01/0.0/0.0/16_019/0000738). J. Petrasek was supported by EU Operational Programme Prague-Competitiveness (no. CZ.2.16/3.1.00/21519). " article_processing_charge: No article_type: original author: - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Melinda F full_name: Abas, Melinda F id: 3CFB3B1C-F248-11E8-B48F-1D18A9856A87 last_name: Abas - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Gergely full_name: Molnar, Gergely id: 34F1AF46-F248-11E8-B48F-1D18A9856A87 last_name: Molnar - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Pavel full_name: Lasák, Pavel last_name: Lasák - first_name: Ivan full_name: Petřík, Ivan last_name: Petřík - first_name: Eugenia full_name: Russinova, Eugenia last_name: Russinova - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Ondřej full_name: Novák, Ondřej last_name: Novák - first_name: Jiří full_name: Pospíšil, Jiří last_name: Pospíšil - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Tan S, Abas MF, Verstraeten I, et al. Salicylic acid targets protein phosphatase 2A to attenuate growth in plants. Current Biology. 2020;30(3):381-395.e8. doi:10.1016/j.cub.2019.11.058 apa: Tan, S., Abas, M. F., Verstraeten, I., Glanc, M., Molnar, G., Hajny, J., … Friml, J. (2020). Salicylic acid targets protein phosphatase 2A to attenuate growth in plants. Current Biology. Cell Press. https://doi.org/10.1016/j.cub.2019.11.058 chicago: Tan, Shutang, Melinda F Abas, Inge Verstraeten, Matous Glanc, Gergely Molnar, Jakub Hajny, Pavel Lasák, et al. “Salicylic Acid Targets Protein Phosphatase 2A to Attenuate Growth in Plants.” Current Biology. Cell Press, 2020. https://doi.org/10.1016/j.cub.2019.11.058. ieee: S. Tan et al., “Salicylic acid targets protein phosphatase 2A to attenuate growth in plants,” Current Biology, vol. 30, no. 3. Cell Press, p. 381–395.e8, 2020. ista: Tan S, Abas MF, Verstraeten I, Glanc M, Molnar G, Hajny J, Lasák P, Petřík I, Russinova E, Petrášek J, Novák O, Pospíšil J, Friml J. 2020. Salicylic acid targets protein phosphatase 2A to attenuate growth in plants. Current Biology. 30(3), 381–395.e8. mla: Tan, Shutang, et al. “Salicylic Acid Targets Protein Phosphatase 2A to Attenuate Growth in Plants.” Current Biology, vol. 30, no. 3, Cell Press, 2020, p. 381–395.e8, doi:10.1016/j.cub.2019.11.058. short: S. Tan, M.F. Abas, I. Verstraeten, M. Glanc, G. Molnar, J. Hajny, P. Lasák, I. Petřík, E. Russinova, J. Petrášek, O. Novák, J. Pospíšil, J. Friml, Current Biology 30 (2020) 381–395.e8. date_created: 2020-02-02T23:01:00Z date_published: 2020-02-03T00:00:00Z date_updated: 2024-03-27T23:30:37Z day: '03' ddc: - '580' department: - _id: JiFr - _id: EvBe doi: 10.1016/j.cub.2019.11.058 ec_funded: 1 external_id: isi: - '000511287900018' pmid: - '31956021' file: - access_level: open_access checksum: 16f7d51fe28f91c21e4896a2028df40b content_type: application/pdf creator: dernst date_created: 2020-09-22T09:51:28Z date_updated: 2020-09-22T09:51:28Z file_id: '8555' file_name: 2020_CurrentBiology_Tan.pdf file_size: 5360135 relation: main_file success: 1 file_date_updated: 2020-09-22T09:51:28Z has_accepted_license: '1' intvolume: ' 30' isi: 1 issue: '3' language: - iso: eng month: '02' oa: 1 oa_version: Published Version page: 381-395.e8 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme - _id: 256FEF10-B435-11E9-9278-68D0E5697425 grant_number: 723-2015 name: Long Term Fellowship publication: Current Biology publication_identifier: issn: - '09609822' publication_status: published publisher: Cell Press quality_controlled: '1' related_material: record: - id: '8822' relation: dissertation_contains status: public scopus_import: '1' status: public title: Salicylic acid targets protein phosphatase 2A to attenuate growth in plants tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 30 year: '2020' ... --- _id: '7500' abstract: - lang: eng text: "Plant survival depends on vascular tissues, which originate in a self‐organizing manner as strands of cells co‐directionally transporting the plant hormone auxin. The latter phenomenon (also known as auxin canalization) is classically hypothesized to be regulated by auxin itself via the effect of this hormone on the polarity of its own intercellular transport. Correlative observations supported this concept, but molecular insights remain limited.\r\nIn the current study, we established an experimental system based on the model Arabidopsis thaliana, which exhibits auxin transport channels and formation of vasculature strands in response to local auxin application.\r\nOur methodology permits the genetic analysis of auxin canalization under controllable experimental conditions. By utilizing this opportunity, we confirmed the dependence of auxin canalization on a PIN‐dependent auxin transport and nuclear, TIR1/AFB‐mediated auxin signaling. We also show that leaf venation and auxin‐mediated PIN repolarization in the root require TIR1/AFB signaling.\r\nFurther studies based on this experimental system are likely to yield better understanding of the mechanisms underlying auxin transport polarization in other developmental contexts." acknowledgement: We thank Mark Estelle, José M. Alonso and the Arabidopsis Stock Centre for providing seeds. We acknowledge the core facility CELLIM of CEITEC supported by the MEYS CR (LM2015062 Czech‐BioImaging) and Plant Sciences Core Facility of CEITEC Masaryk University for help in generating essential data. This project received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement no. 742985) and the Czech Science Foundation GAČR (GA13‐40637S and GA18‐26981S) to JF. JH is the recipient of a DOC Fellowship of the Austrian Academy of Sciences at the Institute of Science and Technology. The authors declare no competing interests. article_processing_charge: No article_type: original author: - first_name: E full_name: Mazur, E last_name: Mazur - first_name: Ivan full_name: Kulik, Ivan id: F0AB3FCE-02D1-11E9-BD0E-99399A5D3DEB last_name: Kulik - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Mazur E, Kulik I, Hajny J, Friml J. Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis. New Phytologist. 2020;226(5):1375-1383. doi:10.1111/nph.16446 apa: Mazur, E., Kulik, I., Hajny, J., & Friml, J. (2020). Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis. New Phytologist. Wiley. https://doi.org/10.1111/nph.16446 chicago: Mazur, E, Ivan Kulik, Jakub Hajny, and Jiří Friml. “Auxin Canalization and Vascular Tissue Formation by TIR1/AFB-Mediated Auxin Signaling in Arabidopsis.” New Phytologist. Wiley, 2020. https://doi.org/10.1111/nph.16446. ieee: E. Mazur, I. Kulik, J. Hajny, and J. Friml, “Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis,” New Phytologist, vol. 226, no. 5. Wiley, pp. 1375–1383, 2020. ista: Mazur E, Kulik I, Hajny J, Friml J. 2020. Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis. New Phytologist. 226(5), 1375–1383. mla: Mazur, E., et al. “Auxin Canalization and Vascular Tissue Formation by TIR1/AFB-Mediated Auxin Signaling in Arabidopsis.” New Phytologist, vol. 226, no. 5, Wiley, 2020, pp. 1375–83, doi:10.1111/nph.16446. short: E. Mazur, I. Kulik, J. Hajny, J. Friml, New Phytologist 226 (2020) 1375–1383. date_created: 2020-02-18T10:03:47Z date_published: 2020-06-01T00:00:00Z date_updated: 2024-03-27T23:30:37Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/nph.16446 ec_funded: 1 external_id: isi: - '000514939700001' pmid: - '31971254' file: - access_level: open_access checksum: 17de728b0205979feb95ce663ba918c2 content_type: application/pdf creator: dernst date_created: 2020-11-20T09:32:10Z date_updated: 2020-11-20T09:32:10Z file_id: '8781' file_name: 2020_NewPhytologist_Mazur.pdf file_size: 2106888 relation: main_file success: 1 file_date_updated: 2020-11-20T09:32:10Z has_accepted_license: '1' intvolume: ' 226' isi: 1 issue: '5' language: - iso: eng month: '06' oa: 1 oa_version: Published Version page: 1375-1383 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 2699E3D2-B435-11E9-9278-68D0E5697425 grant_number: '25239' name: Cell surface receptor complexes for PIN polarity and auxin-mediated development publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646x publication_status: published publisher: Wiley quality_controlled: '1' related_material: record: - id: '8822' relation: dissertation_contains status: public status: public title: Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 226 year: '2020' ... --- _id: '8822' abstract: - lang: eng text: "Self-organization is a hallmark of plant development manifested e.g. by intricate leaf vein patterns, flexible formation of vasculature during organogenesis or its regeneration following wounding. Spontaneously arising channels transporting the phytohormone auxin, created by coordinated polar localizations of PIN-FORMED 1 (PIN1) auxin exporter, provide positional cues for these as well as other plant patterning processes. To find regulators acting downstream of auxin and the TIR1/AFB auxin signaling pathway essential for PIN1 coordinated polarization during auxin canalization, we performed microarray experiments. Besides the known components of general PIN polarity maintenance, such as PID and PIP5K kinases, we identified and characterized a new regulator of auxin canalization, the transcription factor WRKY DNA-BINDING PROTEIN 23 (WRKY23).\r\nNext, we designed a subsequent microarray experiment to further uncover other molecular players, downstream of auxin-TIR1/AFB-WRKY23 involved in the regulation of auxin-mediated PIN repolarization. We identified a novel and crucial part of the molecular machinery underlying auxin canalization. The auxin-regulated malectin-type receptor-like kinase CAMEL and the associated leucine-rich repeat receptor-like kinase CANAR target and directly phosphorylate PIN auxin transporters. camel and canar mutants are impaired in PIN1 subcellular trafficking and auxin-mediated repolarization leading to defects in auxin transport, ultimately to leaf venation and vasculature regeneration defects. Our results describe the CAMEL-CANAR receptor complex, which is required for auxin feed-back on its own transport and thus for coordinated tissue polarization during auxin canalization." alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 citation: ama: Hajny J. Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration. 2020. doi:10.15479/AT:ISTA:8822 apa: Hajny, J. (2020). Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:8822 chicago: Hajny, Jakub. “Identification and Characterization of the Molecular Machinery of Auxin-Dependent Canalization during Vasculature Formation and Regeneration.” Institute of Science and Technology Austria, 2020. https://doi.org/10.15479/AT:ISTA:8822. ieee: J. Hajny, “Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration,” Institute of Science and Technology Austria, 2020. ista: Hajny J. 2020. Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration. Institute of Science and Technology Austria. mla: Hajny, Jakub. Identification and Characterization of the Molecular Machinery of Auxin-Dependent Canalization during Vasculature Formation and Regeneration. Institute of Science and Technology Austria, 2020, doi:10.15479/AT:ISTA:8822. short: J. Hajny, Identification and Characterization of the Molecular Machinery of Auxin-Dependent Canalization during Vasculature Formation and Regeneration, Institute of Science and Technology Austria, 2020. date_created: 2020-12-01T12:38:18Z date_published: 2020-12-01T00:00:00Z date_updated: 2023-09-19T10:39:33Z day: '01' ddc: - '580' degree_awarded: PhD department: - _id: JiFr doi: 10.15479/AT:ISTA:8822 file: - access_level: closed checksum: 210a9675af5e4c78b0b56d920ac82866 content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: jhajny date_created: 2020-12-04T07:27:52Z date_updated: 2021-07-16T22:30:03Z embargo_to: open_access file_id: '8919' file_name: Jakub Hajný IST Austria final_JH.docx file_size: 91279806 relation: source_file - access_level: open_access checksum: 1781385b4aa73eba89cc76c6172f71d2 content_type: application/pdf creator: jhajny date_created: 2020-12-09T15:04:41Z date_updated: 2021-12-08T23:30:03Z embargo: 2021-12-07 file_id: '8933' file_name: Jakub Hajný IST Austria final_JH-merged without Science.pdf file_size: 68707697 relation: main_file file_date_updated: 2021-12-08T23:30:03Z has_accepted_license: '1' language: - iso: eng month: '12' oa: 1 oa_version: Published Version page: '249' publication_identifier: issn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '7427' relation: part_of_dissertation status: public - id: '6260' relation: part_of_dissertation status: public - id: '7500' relation: part_of_dissertation status: public - id: '191' relation: part_of_dissertation status: public - id: '449' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2020' ... --- _id: '8986' abstract: - lang: eng text: 'Flowering plants display the highest diversity among plant species and have notably shaped terrestrial landscapes. Nonetheless, the evolutionary origin of their unprecedented morphological complexity remains largely an enigma. Here, we show that the coevolution of cis-regulatory and coding regions of PIN-FORMED (PIN) auxin transporters confined their expression to certain cell types and directed their subcellular localization to particular cell sides, which together enabled dynamic auxin gradients across tissues critical to the complex architecture of flowering plants. Extensive intraspecies and interspecies genetic complementation experiments with PINs from green alga up to flowering plant lineages showed that PIN genes underwent three subsequent, critical evolutionary innovations and thus acquired a triple function to regulate the development of three essential components of the flowering plant Arabidopsis: shoot/root, inflorescence, and floral organ. Our work highlights the critical role of functional innovations within the PIN gene family as essential prerequisites for the origin of flowering plants.' acknowledgement: 'We thank C.Löhne (Botanic Gardens, University of Bonn) for providing us with A. trichopoda. We would like to thank T.Han, A.Mally (IST, Austria), and C.Hartinger (University of Oxford) for constructive comment and careful reading. Funding: The research leading to these results has received funding from the European Union’s Horizon 2020 Research and Innovation Programme (ERC grant agreement number 742985), Austrian Science Fund (FWF, grant number I 3630-B25), DOC Fellowship of the Austrian Academy of Sciences, and IST Fellow program. ' article_number: eabc8895 article_processing_charge: No article_type: original author: - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: Lesia full_name: Rodriguez Solovey, Lesia id: 3922B506-F248-11E8-B48F-1D18A9856A87 last_name: Rodriguez Solovey orcid: 0000-0002-7244-7237 - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang Y, Rodriguez Solovey L, Li L, Zhang X, Friml J. Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants. Science Advances. 2020;6(50). doi:10.1126/sciadv.abc8895 apa: Zhang, Y., Rodriguez Solovey, L., Li, L., Zhang, X., & Friml, J. (2020). Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants. Science Advances. AAAS. https://doi.org/10.1126/sciadv.abc8895 chicago: Zhang, Yuzhou, Lesia Rodriguez Solovey, Lanxin Li, Xixi Zhang, and Jiří Friml. “Functional Innovations of PIN Auxin Transporters Mark Crucial Evolutionary Transitions during Rise of Flowering Plants.” Science Advances. AAAS, 2020. https://doi.org/10.1126/sciadv.abc8895. ieee: Y. Zhang, L. Rodriguez Solovey, L. Li, X. Zhang, and J. Friml, “Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants,” Science Advances, vol. 6, no. 50. AAAS, 2020. ista: Zhang Y, Rodriguez Solovey L, Li L, Zhang X, Friml J. 2020. Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants. Science Advances. 6(50), eabc8895. mla: Zhang, Yuzhou, et al. “Functional Innovations of PIN Auxin Transporters Mark Crucial Evolutionary Transitions during Rise of Flowering Plants.” Science Advances, vol. 6, no. 50, eabc8895, AAAS, 2020, doi:10.1126/sciadv.abc8895. short: Y. Zhang, L. Rodriguez Solovey, L. Li, X. Zhang, J. Friml, Science Advances 6 (2020). date_created: 2021-01-03T23:01:23Z date_published: 2020-12-11T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '11' ddc: - '580' department: - _id: JiFr doi: 10.1126/sciadv.abc8895 ec_funded: 1 external_id: isi: - '000599903600014' pmid: - '33310852' file: - access_level: open_access checksum: 5ac2500b191c08ef6dab5327f40ff663 content_type: application/pdf creator: dernst date_created: 2021-01-07T12:44:33Z date_updated: 2021-01-07T12:44:33Z file_id: '8994' file_name: 2020_ScienceAdvances_Zhang.pdf file_size: 10578145 relation: main_file success: 1 file_date_updated: 2021-01-07T12:44:33Z has_accepted_license: '1' intvolume: ' 6' isi: 1 issue: '50' language: - iso: eng month: '12' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 26B4D67E-B435-11E9-9278-68D0E5697425 grant_number: '25351' name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated Rapid Growth Inhibition in Arabidopsis Root' publication: Science Advances publication_identifier: eissn: - 2375-2548 publication_status: published publisher: AAAS quality_controlled: '1' related_material: record: - id: '10083' relation: dissertation_contains status: public scopus_import: '1' status: public title: Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants tmp: image: /images/cc_by_nc.png legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) short: CC BY-NC (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 6 year: '2020' ... --- _id: '8283' abstract: - lang: eng text: 'Drought and salt stress are the main environmental cues affecting the survival, development, distribution, and yield of crops worldwide. MYB transcription factors play a crucial role in plants’ biological processes, but the function of pineapple MYB genes is still obscure. In this study, one of the pineapple MYB transcription factors, AcoMYB4, was isolated and characterized. The results showed that AcoMYB4 is localized in the cell nucleus, and its expression is induced by low temperature, drought, salt stress, and hormonal stimulation, especially by abscisic acid (ABA). Overexpression of AcoMYB4 in rice and Arabidopsis enhanced plant sensitivity to osmotic stress; it led to an increase in the number stomata on leaf surfaces and lower germination rate under salt and drought stress. Furthermore, in AcoMYB4 OE lines, the membrane oxidation index, free proline, and soluble sugar contents were decreased. In contrast, electrolyte leakage and malondialdehyde (MDA) content increased significantly due to membrane injury, indicating higher sensitivity to drought and salinity stresses. Besides the above, both the expression level and activities of several antioxidant enzymes were decreased, indicating lower antioxidant activity in AcoMYB4 transgenic plants. Moreover, under osmotic stress, overexpression of AcoMYB4 inhibited ABA biosynthesis through a decrease in the transcription of genes responsible for ABA synthesis (ABA1 and ABA2) and ABA signal transduction factor ABI5. These results suggest that AcoMYB4 negatively regulates osmotic stress by attenuating cellular ABA biosynthesis and signal transduction pathways. ' acknowledgement: 'We would like to thank the reviewers for their helpful comments on the original manuscript. ' article_number: '5272' article_processing_charge: No article_type: original author: - first_name: Huihuang full_name: Chen, Huihuang last_name: Chen - first_name: Linyi full_name: Lai, Linyi last_name: Lai - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Liping full_name: Liu, Liping last_name: Liu - first_name: Bello Hassan full_name: Jakada, Bello Hassan last_name: Jakada - first_name: Youmei full_name: Huang, Youmei last_name: Huang - first_name: Qing full_name: He, Qing last_name: He - first_name: Mengnan full_name: Chai, Mengnan last_name: Chai - first_name: Xiaoping full_name: Niu, Xiaoping last_name: Niu - first_name: Yuan full_name: Qin, Yuan last_name: Qin citation: ama: Chen H, Lai L, Li L, et al. AcoMYB4, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling. International Journal of Molecular Sciences. 2020;21(16). doi:10.3390/ijms21165727 apa: Chen, H., Lai, L., Li, L., Liu, L., Jakada, B. H., Huang, Y., … Qin, Y. (2020). AcoMYB4, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling. International Journal of Molecular Sciences. MDPI. https://doi.org/10.3390/ijms21165727 chicago: Chen, Huihuang, Linyi Lai, Lanxin Li, Liping Liu, Bello Hassan Jakada, Youmei Huang, Qing He, Mengnan Chai, Xiaoping Niu, and Yuan Qin. “AcoMYB4, an Ananas Comosus L. MYB Transcription Factor, Functions in Osmotic Stress through Negative Regulation of ABA Signaling.” International Journal of Molecular Sciences. MDPI, 2020. https://doi.org/10.3390/ijms21165727. ieee: H. Chen et al., “AcoMYB4, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling,” International Journal of Molecular Sciences, vol. 21, no. 16. MDPI, 2020. ista: Chen H, Lai L, Li L, Liu L, Jakada BH, Huang Y, He Q, Chai M, Niu X, Qin Y. 2020. AcoMYB4, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling. International Journal of Molecular Sciences. 21(16), 5272. mla: Chen, Huihuang, et al. “AcoMYB4, an Ananas Comosus L. MYB Transcription Factor, Functions in Osmotic Stress through Negative Regulation of ABA Signaling.” International Journal of Molecular Sciences, vol. 21, no. 16, 5272, MDPI, 2020, doi:10.3390/ijms21165727. short: H. Chen, L. Lai, L. Li, L. Liu, B.H. Jakada, Y. Huang, Q. He, M. Chai, X. Niu, Y. Qin, International Journal of Molecular Sciences 21 (2020). date_created: 2020-08-24T06:24:03Z date_published: 2020-08-10T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '10' ddc: - '570' department: - _id: JiFr doi: 10.3390/ijms21165727 external_id: isi: - '000565090300001' pmid: - '32785037' file: - access_level: open_access checksum: 03b039244e6ae80580385fd9f577e2b2 content_type: application/pdf creator: cziletti date_created: 2020-08-25T09:53:50Z date_updated: 2020-08-25T09:53:50Z file_id: '8292' file_name: 2020_IntMolecSciences_Chen.pdf file_size: 5718755 relation: main_file success: 1 file_date_updated: 2020-08-25T09:53:50Z has_accepted_license: '1' intvolume: ' 21' isi: 1 issue: '16' language: - iso: eng month: '08' oa: 1 oa_version: Published Version pmid: 1 publication: International Journal of Molecular Sciences publication_identifier: eissn: - '14220067' issn: - '16616596' publication_status: published publisher: MDPI quality_controlled: '1' related_material: record: - id: '10083' relation: dissertation_contains status: public scopus_import: '1' status: public title: AcoMYB4, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 21 year: '2020' ... --- _id: '8139' abstract: - lang: eng text: 'Clathrin-mediated endocytosis (CME) is a crucial cellular process implicated in many aspects of plant growth, development, intra- and inter-cellular signaling, nutrient uptake and pathogen defense. Despite these significant roles, little is known about the precise molecular details of how it functions in planta. In order to facilitate the direct quantitative study of plant CME, here we review current routinely used methods and present refined, standardized quantitative imaging protocols which allow the detailed characterization of CME at multiple scales in plant tissues. These include: (i) an efficient electron microscopy protocol for the imaging of Arabidopsis CME vesicles in situ, thus providing a method for the detailed characterization of the ultra-structure of clathrin-coated vesicles; (ii) a detailed protocol and analysis for quantitative live-cell fluorescence microscopy to precisely examine the temporal interplay of endocytosis components during single CME events; (iii) a semi-automated analysis to allow the quantitative characterization of global internalization of cargos in whole plant tissues; and (iv) an overview and validation of useful genetic and pharmacological tools to interrogate the molecular mechanisms and function of CME in intact plant samples.' acknowledged_ssus: - _id: EM-Fac - _id: Bio acknowledgement: "This paper is dedicated to the memory of Christien Merrifield. He pioneered quantitative\r\nimaging approaches in mammalian CME and his mentorship inspired the development of all\r\nthe analysis methods presented here. His joy in research, pure scientific curiosity and\r\nmicroscopy excellence remain a constant inspiration. We thank Daniel Van Damme for gifting\r\nus the CLC2-GFP x TPLATE-TagRFP plants used in this manuscript. We further thank the\r\nScientific Service Units at IST Austria; specifically, the Electron Microscopy Facility for\r\ntechnical assistance (in particular Vanessa Zheden) and the BioImaging Facility BioImaging\r\nFacility for access to equipment. " article_number: jcs248062 article_processing_charge: No article_type: original author: - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Nataliia full_name: Gnyliukh, Nataliia id: 390C1120-F248-11E8-B48F-1D18A9856A87 last_name: Gnyliukh orcid: 0000-0002-2198-0509 - first_name: Walter full_name: Kaufmann, Walter id: 3F99E422-F248-11E8-B48F-1D18A9856A87 last_name: Kaufmann orcid: 0000-0001-9735-5315 - first_name: Madhumitha full_name: Narasimhan, Madhumitha id: 44BF24D0-F248-11E8-B48F-1D18A9856A87 last_name: Narasimhan orcid: 0000-0002-8600-0671 - first_name: G full_name: Vert, G last_name: Vert - first_name: SY full_name: Bednarek, SY last_name: Bednarek - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Johnson AJ, Gnyliukh N, Kaufmann W, et al. Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis. Journal of Cell Science. 2020;133(15). doi:10.1242/jcs.248062 apa: Johnson, A. J., Gnyliukh, N., Kaufmann, W., Narasimhan, M., Vert, G., Bednarek, S., & Friml, J. (2020). Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis. Journal of Cell Science. The Company of Biologists. https://doi.org/10.1242/jcs.248062 chicago: Johnson, Alexander J, Nataliia Gnyliukh, Walter Kaufmann, Madhumitha Narasimhan, G Vert, SY Bednarek, and Jiří Friml. “Experimental Toolbox for Quantitative Evaluation of Clathrin-Mediated Endocytosis in the Plant Model Arabidopsis.” Journal of Cell Science. The Company of Biologists, 2020. https://doi.org/10.1242/jcs.248062. ieee: A. J. Johnson et al., “Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis,” Journal of Cell Science, vol. 133, no. 15. The Company of Biologists, 2020. ista: Johnson AJ, Gnyliukh N, Kaufmann W, Narasimhan M, Vert G, Bednarek S, Friml J. 2020. Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis. Journal of Cell Science. 133(15), jcs248062. mla: Johnson, Alexander J., et al. “Experimental Toolbox for Quantitative Evaluation of Clathrin-Mediated Endocytosis in the Plant Model Arabidopsis.” Journal of Cell Science, vol. 133, no. 15, jcs248062, The Company of Biologists, 2020, doi:10.1242/jcs.248062. short: A.J. Johnson, N. Gnyliukh, W. Kaufmann, M. Narasimhan, G. Vert, S. Bednarek, J. Friml, Journal of Cell Science 133 (2020). date_created: 2020-07-21T08:58:19Z date_published: 2020-08-06T00:00:00Z date_updated: 2023-12-01T13:51:07Z day: '06' ddc: - '575' department: - _id: JiFr - _id: EM-Fac doi: 10.1242/jcs.248062 ec_funded: 1 external_id: isi: - '000561047900021' pmid: - '32616560' file: - access_level: open_access checksum: 2d11f79a0b4e0a380fb002b933da331a content_type: application/pdf creator: ajohnson date_created: 2020-11-26T17:12:51Z date_updated: 2021-08-08T22:30:03Z embargo: 2021-08-07 file_id: '8815' file_name: 2020 - Johnson - JSC - plant CME toolbox.pdf file_size: 15150403 relation: main_file file_date_updated: 2021-08-08T22:30:03Z has_accepted_license: '1' intvolume: ' 133' isi: 1 issue: '15' language: - iso: eng month: '08' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program publication: Journal of Cell Science publication_identifier: eissn: - 1477-9137 issn: - 0021-9533 publication_status: published publisher: The Company of Biologists quality_controlled: '1' related_material: record: - id: '14510' relation: dissertation_contains status: public scopus_import: '1' status: public title: Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 133 year: '2020' ... --- _id: '5908' abstract: - lang: eng text: The interorganelle communication mediated by membrane contact sites (MCSs) is an evolutionary hallmark of eukaryotic cells. MCS connections enable the nonvesicular exchange of information between organelles and allow them to coordinate responses to changing cellular environments. In plants, the importance of MCS components in the responses to environmental stress has been widely established, but the molecular mechanisms regulating interorganelle connectivity during stress still remain opaque. In this report, we use the model plant Arabidopsis thaliana to show that ionic stress increases endoplasmic reticulum (ER)–plasma membrane (PM) connectivity by promoting the cortical expansion of synaptotagmin 1 (SYT1)-enriched ER–PM contact sites (S-EPCSs). We define differential roles for the cortical cytoskeleton in the regulation of S-EPCS dynamics and ER–PM connectivity, and we identify the accumulation of phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] at the PM as a molecular signal associated with the ER–PM connectivity changes. Our study highlights the functional conservation of EPCS components and PM phosphoinositides as modulators of ER–PM connectivity in eukaryotes, and uncovers unique aspects of the spatiotemporal regulation of ER–PM connectivity in plants. article_processing_charge: No article_type: original author: - first_name: Eunkyoung full_name: Lee, Eunkyoung last_name: Lee - first_name: Steffen full_name: Vanneste, Steffen last_name: Vanneste - first_name: Jessica full_name: Pérez-Sancho, Jessica last_name: Pérez-Sancho - first_name: Francisco full_name: Benitez-Fuente, Francisco last_name: Benitez-Fuente - first_name: Matthew full_name: Strelau, Matthew last_name: Strelau - first_name: Alberto P. full_name: Macho, Alberto P. last_name: Macho - first_name: Miguel A. full_name: Botella, Miguel A. last_name: Botella - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Abel full_name: Rosado, Abel last_name: Rosado citation: ama: Lee E, Vanneste S, Pérez-Sancho J, et al. Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. 2019;116(4):1420-1429. doi:10.1073/pnas.1818099116 apa: Lee, E., Vanneste, S., Pérez-Sancho, J., Benitez-Fuente, F., Strelau, M., Macho, A. P., … Rosado, A. (2019). Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. National Academy of Sciences. https://doi.org/10.1073/pnas.1818099116 chicago: Lee, Eunkyoung, Steffen Vanneste, Jessica Pérez-Sancho, Francisco Benitez-Fuente, Matthew Strelau, Alberto P. Macho, Miguel A. Botella, Jiří Friml, and Abel Rosado. “Ionic Stress Enhances ER–PM Connectivity via Phosphoinositide-Associated SYT1 Contact Site Expansion in Arabidopsis.” Proceedings of the National Academy of Sciences of the United States of America. National Academy of Sciences, 2019. https://doi.org/10.1073/pnas.1818099116. ieee: E. Lee et al., “Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 4. National Academy of Sciences, pp. 1420–1429, 2019. ista: Lee E, Vanneste S, Pérez-Sancho J, Benitez-Fuente F, Strelau M, Macho AP, Botella MA, Friml J, Rosado A. 2019. Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. 116(4), 1420–1429. mla: Lee, Eunkyoung, et al. “Ionic Stress Enhances ER–PM Connectivity via Phosphoinositide-Associated SYT1 Contact Site Expansion in Arabidopsis.” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 4, National Academy of Sciences, 2019, pp. 1420–29, doi:10.1073/pnas.1818099116. short: E. Lee, S. Vanneste, J. Pérez-Sancho, F. Benitez-Fuente, M. Strelau, A.P. Macho, M.A. Botella, J. Friml, A. Rosado, Proceedings of the National Academy of Sciences of the United States of America 116 (2019) 1420–1429. date_created: 2019-02-03T22:59:14Z date_published: 2019-01-22T00:00:00Z date_updated: 2023-08-24T14:31:09Z day: '22' department: - _id: JiFr doi: 10.1073/pnas.1818099116 external_id: isi: - '000456336100050' pmid: - '30610176' intvolume: ' 116' isi: 1 issue: '4' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1073/pnas.1818099116 month: '01' oa: 1 oa_version: Published Version page: 1420-1429 pmid: 1 publication: Proceedings of the National Academy of Sciences of the United States of America publication_status: published publisher: National Academy of Sciences quality_controlled: '1' scopus_import: '1' status: public title: Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 116 year: '2019' ... --- _id: '6023' abstract: - lang: eng text: Multicellular development requires coordinated cell polarization relative to body axes, and translation to oriented cell division 1–3 . In plants, it is unknown how cell polarities are connected to organismal axes and translated to division. Here, we identify Arabidopsis SOSEKI proteins that integrate apical–basal and radial organismal axes to localize to polar cell edges. Localization does not depend on tissue context, requires cell wall integrity and is defined by a transferrable, protein-specific motif. A Domain of Unknown Function in SOSEKI proteins resembles the DIX oligomerization domain in the animal Dishevelled polarity regulator. The DIX-like domain self-interacts and is required for edge localization and for influencing division orientation, together with a second domain that defines the polar membrane domain. Our work shows that SOSEKI proteins locally interpret global polarity cues and can influence cell division orientation. Furthermore, this work reveals that, despite fundamental differences, cell polarity mechanisms in plants and animals converge on a similar protein domain. article_processing_charge: No author: - first_name: Saiko full_name: Yoshida, Saiko id: 2E46069C-F248-11E8-B48F-1D18A9856A87 last_name: Yoshida - first_name: Alja full_name: Van Der Schuren, Alja last_name: Van Der Schuren - first_name: Maritza full_name: Van Dop, Maritza last_name: Van Dop - first_name: Luc full_name: Van Galen, Luc last_name: Van Galen - first_name: Shunsuke full_name: Saiga, Shunsuke last_name: Saiga - first_name: Milad full_name: Adibi, Milad last_name: Adibi - first_name: Barbara full_name: Möller, Barbara last_name: Möller - first_name: Colette A. full_name: Ten Hove, Colette A. last_name: Ten Hove - first_name: Peter full_name: Marhavy, Peter id: 3F45B078-F248-11E8-B48F-1D18A9856A87 last_name: Marhavy orcid: 0000-0001-5227-5741 - first_name: Richard full_name: Smith, Richard last_name: Smith - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Dolf full_name: Weijers, Dolf last_name: Weijers citation: ama: Yoshida S, Van Der Schuren A, Van Dop M, et al. A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis. Nature Plants. 2019;5(2):160-166. doi:10.1038/s41477-019-0363-6 apa: Yoshida, S., Van Der Schuren, A., Van Dop, M., Van Galen, L., Saiga, S., Adibi, M., … Weijers, D. (2019). A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis. Nature Plants. Springer Nature. https://doi.org/10.1038/s41477-019-0363-6 chicago: Yoshida, Saiko, Alja Van Der Schuren, Maritza Van Dop, Luc Van Galen, Shunsuke Saiga, Milad Adibi, Barbara Möller, et al. “A SOSEKI-Based Coordinate System Interprets Global Polarity Cues in Arabidopsis.” Nature Plants. Springer Nature, 2019. https://doi.org/10.1038/s41477-019-0363-6. ieee: S. Yoshida et al., “A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis,” Nature Plants, vol. 5, no. 2. Springer Nature, pp. 160–166, 2019. ista: Yoshida S, Van Der Schuren A, Van Dop M, Van Galen L, Saiga S, Adibi M, Möller B, Ten Hove CA, Marhavý P, Smith R, Friml J, Weijers D. 2019. A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis. Nature Plants. 5(2), 160–166. mla: Yoshida, Saiko, et al. “A SOSEKI-Based Coordinate System Interprets Global Polarity Cues in Arabidopsis.” Nature Plants, vol. 5, no. 2, Springer Nature, 2019, pp. 160–66, doi:10.1038/s41477-019-0363-6. short: S. Yoshida, A. Van Der Schuren, M. Van Dop, L. Van Galen, S. Saiga, M. Adibi, B. Möller, C.A. Ten Hove, P. Marhavý, R. Smith, J. Friml, D. Weijers, Nature Plants 5 (2019) 160–166. date_created: 2019-02-17T22:59:21Z date_published: 2019-02-08T00:00:00Z date_updated: 2023-08-24T14:46:47Z day: '08' department: - _id: JiFr - _id: EvBe doi: 10.1038/s41477-019-0363-6 ec_funded: 1 external_id: isi: - '000460479600014' intvolume: ' 5' isi: 1 issue: '2' language: - iso: eng main_file_link: - open_access: '1' url: https://www.biorxiv.org/content/10.1101/479113v1.abstract month: '02' oa: 1 oa_version: Submitted Version page: 160-166 project: - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme publication: Nature Plants publication_status: published publisher: Springer Nature quality_controlled: '1' scopus_import: '1' status: public title: A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 5 year: '2019' ... --- _id: '6104' abstract: - lang: eng text: Abiotic stress poses constant challenges for plant survival and is a serious problem for global agricultural productivity. On a molecular level, stress conditions result in elevation of reactive oxygen species (ROS) production causing oxidative stress associated with oxidation of proteins and nucleic acids as well as impairment of membrane functions. Adaptation of root growth to ROS accumulation is facilitated through modification of auxin and cytokinin hormone homeostasis. Here, we report that in Arabidopsis root meristem, ROS-induced changes of auxin levels correspond to decreased abundance of PIN auxin efflux carriers at the plasma membrane (PM). Specifically, increase in H2O2 levels affects PIN2 endocytic recycling. We show that the PIN2 intracellular trafficking during adaptation to oxidative stress requires the function of the ADP-ribosylation factor (ARF)-guanine-nucleotide exchange factor (GEF) BEN1, an actin-associated regulator of the trafficking from the PM to early endosomes and, presumably, indirectly, trafficking to the vacuoles. We propose that H2O2 levels affect the actin dynamics thus modulating ARF-GEF-dependent trafficking of PIN2. This mechanism provides a way how root growth acclimates to stress and adapts to a changing environment. article_processing_charge: No author: - first_name: Marta full_name: Zwiewka, Marta last_name: Zwiewka - first_name: Agnieszka full_name: Bielach, Agnieszka last_name: Bielach - first_name: Prashanth full_name: Tamizhselvan, Prashanth last_name: Tamizhselvan - first_name: Sharmila full_name: Madhavan, Sharmila last_name: Madhavan - first_name: Eman Elrefaay full_name: Ryad, Eman Elrefaay last_name: Ryad - first_name: Shutang full_name: Tan, Shutang id: 2DE75584-F248-11E8-B48F-1D18A9856A87 last_name: Tan orcid: 0000-0002-0471-8285 - first_name: Mónika full_name: Hrtyan, Mónika id: 45A71A74-F248-11E8-B48F-1D18A9856A87 last_name: Hrtyan - first_name: Petre full_name: Dobrev, Petre last_name: Dobrev - first_name: Radomira full_name: Vanková, Radomira last_name: Vanková - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Vanesa B. full_name: Tognetti, Vanesa B. last_name: Tognetti citation: ama: Zwiewka M, Bielach A, Tamizhselvan P, et al. Root adaptation to H2O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking. Plant and Cell Physiology. 2019;60(2):255-273. doi:10.1093/pcp/pcz001 apa: Zwiewka, M., Bielach, A., Tamizhselvan, P., Madhavan, S., Ryad, E. E., Tan, S., … Tognetti, V. B. (2019). Root adaptation to H2O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking. Plant and Cell Physiology. Oxford University Press. https://doi.org/10.1093/pcp/pcz001 chicago: Zwiewka, Marta, Agnieszka Bielach, Prashanth Tamizhselvan, Sharmila Madhavan, Eman Elrefaay Ryad, Shutang Tan, Mónika Hrtyan, et al. “Root Adaptation to H2O2-Induced Oxidative Stress by ARF-GEF BEN1- and Cytoskeleton-Mediated PIN2 Trafficking.” Plant and Cell Physiology. Oxford University Press, 2019. https://doi.org/10.1093/pcp/pcz001. ieee: M. Zwiewka et al., “Root adaptation to H2O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking,” Plant and Cell Physiology, vol. 60, no. 2. Oxford University Press, pp. 255–273, 2019. ista: Zwiewka M, Bielach A, Tamizhselvan P, Madhavan S, Ryad EE, Tan S, Hrtyan M, Dobrev P, Vanková R, Friml J, Tognetti VB. 2019. Root adaptation to H2O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking. Plant and Cell Physiology. 60(2), 255–273. mla: Zwiewka, Marta, et al. “Root Adaptation to H2O2-Induced Oxidative Stress by ARF-GEF BEN1- and Cytoskeleton-Mediated PIN2 Trafficking.” Plant and Cell Physiology, vol. 60, no. 2, Oxford University Press, 2019, pp. 255–73, doi:10.1093/pcp/pcz001. short: M. Zwiewka, A. Bielach, P. Tamizhselvan, S. Madhavan, E.E. Ryad, S. Tan, M. Hrtyan, P. Dobrev, R. Vanková, J. Friml, V.B. Tognetti, Plant and Cell Physiology 60 (2019) 255–273. date_created: 2019-03-17T22:59:14Z date_published: 2019-02-01T00:00:00Z date_updated: 2023-08-25T08:05:28Z day: '01' department: - _id: JiFr doi: 10.1093/pcp/pcz001 external_id: isi: - '000459634300002' pmid: - '30668780' intvolume: ' 60' isi: 1 issue: '2' language: - iso: eng month: '02' oa_version: None page: 255-273 pmid: 1 publication: Plant and Cell Physiology publication_identifier: eissn: - 1471-9053 issn: - 0032-0781 publication_status: published publisher: Oxford University Press quality_controlled: '1' scopus_import: '1' status: public title: Root adaptation to H2O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 60 year: '2019' ... --- _id: '6262' abstract: - lang: eng text: "Gravitropism is an adaptive response that orients plant growth parallel to the gravity vector. Asymmetric\r\ndistribution of the phytohormone auxin is a necessary prerequisite to the tropic bending both in roots and\r\nshoots. During hypocotyl gravitropic response, the PIN3 auxin transporter polarizes within gravity-sensing\r\ncells to redirect intercellular auxin fluxes. First gravity-induced PIN3 polarization to the bottom cell mem-\r\nbranes leads to the auxin accumulation at the lower side of the organ, initiating bending and, later, auxin\r\nfeedback-mediated repolarization restores symmetric auxin distribution to terminate bending. Here, we per-\r\nformed a forward genetic screen to identify regulators of both PIN3 polarization events during gravitropic\r\nresponse. We searched for mutants with defective PIN3 polarizations based on easy-to-score morphological\r\noutputs of decreased or increased gravity-induced hypocotyl bending. We identified the number of\r\nhypocotyl reduced bending (hrb) and hypocotyl hyperbending (hhb) mutants, revealing that reduced bending corre-\r\nlated typically with defective gravity-induced PIN3 relocation whereas all analyzed hhb mutants showed\r\ndefects in the second, auxin-mediated PIN3 relocation. Next-generation sequencing-aided mutation map-\r\nping identified several candidate genes, including SCARECROW and ACTIN2, revealing roles of endodermis\r\nspecification and actin cytoskeleton in the respective gravity- and auxin-induced PIN polarization events.\r\nThe hypocotyl gravitropism screen thus promises to provide novel insights into mechanisms underlying cell\r\npolarity and plant adaptive development." article_processing_charge: Yes (via OA deal) article_type: original author: - first_name: Hana full_name: Rakusová, Hana last_name: Rakusová - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: Petr full_name: Valošek, Petr id: 3CDB6F94-F248-11E8-B48F-1D18A9856A87 last_name: Valošek - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Rakusová H, Han H, Valošek P, Friml J. Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls. The Plant Journal. 2019;98(6):1048-1059. doi:10.1111/tpj.14301 apa: Rakusová, H., Han, H., Valošek, P., & Friml, J. (2019). Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls. The Plant Journal. Wiley. https://doi.org/10.1111/tpj.14301 chicago: Rakusová, Hana, Huibin Han, Petr Valošek, and Jiří Friml. “Genetic Screen for Factors Mediating PIN Polarization in Gravistimulated Arabidopsis Thaliana Hypocotyls.” The Plant Journal. Wiley, 2019. https://doi.org/10.1111/tpj.14301. ieee: H. Rakusová, H. Han, P. Valošek, and J. Friml, “Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls,” The Plant Journal, vol. 98, no. 6. Wiley, pp. 1048–1059, 2019. ista: Rakusová H, Han H, Valošek P, Friml J. 2019. Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls. The Plant Journal. 98(6), 1048–1059. mla: Rakusová, Hana, et al. “Genetic Screen for Factors Mediating PIN Polarization in Gravistimulated Arabidopsis Thaliana Hypocotyls.” The Plant Journal, vol. 98, no. 6, Wiley, 2019, pp. 1048–59, doi:10.1111/tpj.14301. short: H. Rakusová, H. Han, P. Valošek, J. Friml, The Plant Journal 98 (2019) 1048–1059. date_created: 2019-04-09T08:46:44Z date_published: 2019-06-01T00:00:00Z date_updated: 2023-08-25T10:11:03Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/tpj.14301 ec_funded: 1 external_id: isi: - '000473644100008' pmid: - '30821050' file: - access_level: open_access checksum: ad3b5e270b67ba2a45f894ce3be27920 content_type: application/pdf creator: dernst date_created: 2019-04-15T09:38:43Z date_updated: 2020-07-14T12:47:25Z file_id: '6304' file_name: 2019_PlantJournal_Rakusov.pdf file_size: 1383100 relation: main_file file_date_updated: 2020-07-14T12:47:25Z has_accepted_license: '1' intvolume: ' 98' isi: 1 issue: '6' language: - iso: eng month: '06' oa: 1 oa_version: Published Version page: 1048-1059 pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: The Plant Journal publication_identifier: eissn: - 1365-313x issn: - 0960-7412 publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 98 year: '2019' ... --- _id: '6261' abstract: - lang: eng text: Nitrate regulation of root stem cell activity is auxin-dependent. article_processing_charge: No article_type: letter_note author: - first_name: Y full_name: Wang, Y last_name: Wang - first_name: Z full_name: Gong, Z last_name: Gong - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: J full_name: Zhang, J last_name: Zhang citation: ama: Wang Y, Gong Z, Friml J, Zhang J. Nitrate modulates the differentiation of root distal stem cells. Plant Physiology. 2019;180(1):22-25. doi:10.1104/pp.18.01305 apa: Wang, Y., Gong, Z., Friml, J., & Zhang, J. (2019). Nitrate modulates the differentiation of root distal stem cells. Plant Physiology. ASPB. https://doi.org/10.1104/pp.18.01305 chicago: Wang, Y, Z Gong, Jiří Friml, and J Zhang. “Nitrate Modulates the Differentiation of Root Distal Stem Cells.” Plant Physiology. ASPB, 2019. https://doi.org/10.1104/pp.18.01305. ieee: Y. Wang, Z. Gong, J. Friml, and J. Zhang, “Nitrate modulates the differentiation of root distal stem cells,” Plant Physiology, vol. 180, no. 1. ASPB, pp. 22–25, 2019. ista: Wang Y, Gong Z, Friml J, Zhang J. 2019. Nitrate modulates the differentiation of root distal stem cells. Plant Physiology. 180(1), 22–25. mla: Wang, Y., et al. “Nitrate Modulates the Differentiation of Root Distal Stem Cells.” Plant Physiology, vol. 180, no. 1, ASPB, 2019, pp. 22–25, doi:10.1104/pp.18.01305. short: Y. Wang, Z. Gong, J. Friml, J. Zhang, Plant Physiology 180 (2019) 22–25. date_created: 2019-04-09T08:46:17Z date_published: 2019-05-01T00:00:00Z date_updated: 2023-08-25T10:10:23Z day: '01' department: - _id: JiFr doi: 10.1104/pp.18.01305 external_id: isi: - '000466860800010' pmid: - '30787134' intvolume: ' 180' isi: 1 issue: '1' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1104/pp.18.01305 month: '05' oa: 1 oa_version: Published Version page: 22-25 pmid: 1 publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: ASPB quality_controlled: '1' scopus_import: '1' status: public title: Nitrate modulates the differentiation of root distal stem cells type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 180 year: '2019' ... --- _id: '6504' abstract: - lang: eng text: "Root gravitropism is one of the most important processes allowing plant adaptation to the land environment. Auxin plays a central role in mediating root gravitropism, but how auxin contributes to gravitational perception and the subsequent response is still unclear.\r\n\r\nHere, we showed that the local auxin maximum/gradient within the root apex, which is generated by the PIN directional auxin transporters, regulates the expression of three key starch granule synthesis genes, SS4, PGM and ADG1, which in turn influence the accumulation of starch granules that serve as a statolith perceiving gravity.\r\n\r\nMoreover, using the cvxIAA‐ccvTIR1 system, we also showed that TIR1‐mediated auxin signaling is required for starch granule formation and gravitropic response within root tips. In addition, axr3 mutants showed reduced auxin‐mediated starch granule accumulation and disruption of gravitropism within the root apex.\r\n\r\nOur results indicate that auxin‐mediated statolith production relies on the TIR1/AFB‐AXR3‐mediated auxin signaling pathway. In summary, we propose a dual role for auxin in gravitropism: the regulation of both gravity perception and response." article_processing_charge: No article_type: original author: - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: P full_name: He, P last_name: He - first_name: X full_name: Ma, X last_name: Ma - first_name: Z full_name: Yang, Z last_name: Yang - first_name: C full_name: Pang, C last_name: Pang - first_name: J full_name: Yu, J last_name: Yu - first_name: G full_name: Wang, G last_name: Wang - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: G full_name: Xiao, G last_name: Xiao citation: ama: Zhang Y, He P, Ma X, et al. Auxin-mediated statolith production for root gravitropism. New Phytologist. 2019;224(2):761-774. doi:10.1111/nph.15932 apa: Zhang, Y., He, P., Ma, X., Yang, Z., Pang, C., Yu, J., … Xiao, G. (2019). Auxin-mediated statolith production for root gravitropism. New Phytologist. Wiley. https://doi.org/10.1111/nph.15932 chicago: Zhang, Yuzhou, P He, X Ma, Z Yang, C Pang, J Yu, G Wang, Jiří Friml, and G Xiao. “Auxin-Mediated Statolith Production for Root Gravitropism.” New Phytologist. Wiley, 2019. https://doi.org/10.1111/nph.15932. ieee: Y. Zhang et al., “Auxin-mediated statolith production for root gravitropism,” New Phytologist, vol. 224, no. 2. Wiley, pp. 761–774, 2019. ista: Zhang Y, He P, Ma X, Yang Z, Pang C, Yu J, Wang G, Friml J, Xiao G. 2019. Auxin-mediated statolith production for root gravitropism. New Phytologist. 224(2), 761–774. mla: Zhang, Yuzhou, et al. “Auxin-Mediated Statolith Production for Root Gravitropism.” New Phytologist, vol. 224, no. 2, Wiley, 2019, pp. 761–74, doi:10.1111/nph.15932. short: Y. Zhang, P. He, X. Ma, Z. Yang, C. Pang, J. Yu, G. Wang, J. Friml, G. Xiao, New Phytologist 224 (2019) 761–774. date_created: 2019-05-28T14:33:26Z date_published: 2019-10-01T00:00:00Z date_updated: 2023-08-28T08:40:13Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/nph.15932 external_id: isi: - '000487184200024' pmid: - '31111487' file: - access_level: open_access checksum: 6488243334538f5c39099a701cbf76b9 content_type: application/pdf creator: dernst date_created: 2020-10-14T08:59:33Z date_updated: 2020-10-14T08:59:33Z file_id: '8661' file_name: 2019_NewPhytologist_Zhang_accepted.pdf file_size: 1099061 relation: main_file success: 1 file_date_updated: 2020-10-14T08:59:33Z has_accepted_license: '1' intvolume: ' 224' isi: 1 issue: '2' language: - iso: eng month: '10' oa: 1 oa_version: Submitted Version page: 761-774 pmid: 1 publication: New Phytologist publication_identifier: eissn: - 1469-8137 issn: - 0028-646x publication_status: published publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: Auxin-mediated statolith production for root gravitropism type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 224 year: '2019' ... --- _id: '6611' abstract: - lang: eng text: 'Cell polarity is crucial for the coordinated development of all multicellular organisms. In plants, this is exemplified by the PIN-FORMED (PIN) efflux carriers of the phytohormone auxin: The polar subcellular localization of the PINs is instructive to the directional intercellular auxin transport, and thus to a plethora of auxin-regulated growth and developmental processes. Despite its importance, the regulation of PIN polar subcellular localization remains poorly understood. Here, we have employed advanced live-cell imaging techniques to study the roles of microtubules and actin microfilaments in the establishment of apical polar localization of PIN2 in the epidermis of the Arabidopsis root meristem. We report that apical PIN2 polarity requires neither intact actin microfilaments nor microtubules, suggesting that the primary spatial cue for polar PIN distribution is likely independent of cytoskeleton-guided endomembrane trafficking.' acknowledged_ssus: - _id: Bio article_number: '222' article_processing_charge: No author: - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Glanc M, Fendrych M, Friml J. PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton. Biomolecules. 2019;9(6). doi:10.3390/biom9060222 apa: Glanc, M., Fendrych, M., & Friml, J. (2019). PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton. Biomolecules. MDPI. https://doi.org/10.3390/biom9060222 chicago: Glanc, Matous, Matyas Fendrych, and Jiří Friml. “PIN2 Polarity Establishment in Arabidopsis in the Absence of an Intact Cytoskeleton.” Biomolecules. MDPI, 2019. https://doi.org/10.3390/biom9060222. ieee: M. Glanc, M. Fendrych, and J. Friml, “PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton,” Biomolecules, vol. 9, no. 6. MDPI, 2019. ista: Glanc M, Fendrych M, Friml J. 2019. PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton. Biomolecules. 9(6), 222. mla: Glanc, Matous, et al. “PIN2 Polarity Establishment in Arabidopsis in the Absence of an Intact Cytoskeleton.” Biomolecules, vol. 9, no. 6, 222, MDPI, 2019, doi:10.3390/biom9060222. short: M. Glanc, M. Fendrych, J. Friml, Biomolecules 9 (2019). date_created: 2019-07-07T21:59:21Z date_published: 2019-06-07T00:00:00Z date_updated: 2023-08-28T12:30:24Z day: '07' ddc: - '580' department: - _id: JiFr doi: 10.3390/biom9060222 ec_funded: 1 external_id: isi: - '000475301500018' pmid: - '31181636' file: - access_level: open_access checksum: 1ce1bd36038fe5381057a1bcc6760083 content_type: application/pdf creator: kschuh date_created: 2019-07-08T15:46:32Z date_updated: 2020-07-14T12:47:34Z file_id: '6625' file_name: biomolecules-2019-Matous.pdf file_size: 1066773 relation: main_file file_date_updated: 2020-07-14T12:47:34Z has_accepted_license: '1' intvolume: ' 9' isi: 1 issue: '6' language: - iso: eng month: '06' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Biomolecules publication_status: published publisher: MDPI quality_controlled: '1' scopus_import: '1' status: public title: PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 9 year: '2019' ... --- _id: '6778' abstract: - lang: eng text: "An important adaptation during colonization of land by plants is gravitropic growth of roots, which enabled roots to reach water and nutrients, and firmly anchor plants in the ground. Here we provide insights into the evolution of an efficient root gravitropic mechanism in the seed plants. Architectural innovation, with gravity perception constrained in the root tips\r\nalong with a shootward transport route for the phytohormone auxin, appeared only upon the emergence of seed plants. Interspecies complementation and protein domain swapping revealed functional innovations within the PIN family of auxin transporters leading to the evolution of gravitropism-specific PINs. The unique apical/shootward subcellular localization of PIN proteins is the major evolutionary innovation that connected the anatomically separated sites of gravity perception and growth response via the mobile auxin signal. We conclude that the crucial anatomical and functional components emerged hand-in-hand to facilitate the evolution of fast gravitropic response, which is one of the major adaptations of seed plants to dry land." article_number: '3480' article_processing_charge: No article_type: original author: - first_name: Yuzhou full_name: Zhang, Yuzhou id: 3B6137F2-F248-11E8-B48F-1D18A9856A87 last_name: Zhang orcid: 0000-0003-2627-6956 - first_name: G full_name: Xiao, G last_name: Xiao - first_name: X full_name: Wang, X last_name: Wang - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Zhang Y, Xiao G, Wang X, Zhang X, Friml J. Evolution of fast root gravitropism in seed plants. Nature Communications. 2019;10. doi:10.1038/s41467-019-11471-8 apa: Zhang, Y., Xiao, G., Wang, X., Zhang, X., & Friml, J. (2019). Evolution of fast root gravitropism in seed plants. Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-019-11471-8 chicago: Zhang, Yuzhou, G Xiao, X Wang, Xixi Zhang, and Jiří Friml. “Evolution of Fast Root Gravitropism in Seed Plants.” Nature Communications. Springer Nature, 2019. https://doi.org/10.1038/s41467-019-11471-8. ieee: Y. Zhang, G. Xiao, X. Wang, X. Zhang, and J. Friml, “Evolution of fast root gravitropism in seed plants,” Nature Communications, vol. 10. Springer Nature, 2019. ista: Zhang Y, Xiao G, Wang X, Zhang X, Friml J. 2019. Evolution of fast root gravitropism in seed plants. Nature Communications. 10, 3480. mla: Zhang, Yuzhou, et al. “Evolution of Fast Root Gravitropism in Seed Plants.” Nature Communications, vol. 10, 3480, Springer Nature, 2019, doi:10.1038/s41467-019-11471-8. short: Y. Zhang, G. Xiao, X. Wang, X. Zhang, J. Friml, Nature Communications 10 (2019). date_created: 2019-08-09T08:46:26Z date_published: 2019-08-02T00:00:00Z date_updated: 2023-08-29T07:02:44Z day: '02' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41467-019-11471-8 ec_funded: 1 external_id: isi: - '000478576500012' pmid: - '31375675' file: - access_level: open_access checksum: d2c654fdb97f33078f606fe0c298bf6e content_type: application/pdf creator: dernst date_created: 2019-08-12T07:09:20Z date_updated: 2020-07-14T12:47:40Z file_id: '6798' file_name: 2019_NatureComm_Zhang.pdf file_size: 6406141 relation: main_file file_date_updated: 2020-07-14T12:47:40Z has_accepted_license: '1' intvolume: ' 10' isi: 1 language: - iso: eng month: '08' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme publication: Nature Communications publication_identifier: issn: - 2041-1723 publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/when-plant-roots-learned-to-follow-gravity/ scopus_import: '1' status: public title: Evolution of fast root gravitropism in seed plants tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 10 year: '2019' ... --- _id: '6366' abstract: - lang: eng text: Plants have a remarkable capacity to adjust their growth and development to elevated ambient temperatures. Increased elongation growth of roots, hypocotyls and petioles in warm temperatures are hallmarks of seedling thermomorphogenesis. In the last decade, significant progress has been made to identify the molecular signaling components regulating these growth responses. Increased ambient temperature utilizes diverse components of the light sensing and signal transduction network to trigger growth adjustments. However, it remains unknown whether temperature sensing and responses are universal processes that occur uniformly in all plant organs. Alternatively, temperature sensing may be confined to specific tissues or organs, which would require a systemic signal that mediates responses in distal parts of the plant. Here we show that Arabidopsis (Arabidopsis thaliana) seedlings show organ-specific transcriptome responses to elevated temperatures, and that thermomorphogenesis involves both autonomous and organ-interdependent temperature sensing and signaling. Seedling roots can sense and respond to temperature in a shoot-independent manner, whereas shoot temperature responses require both local and systemic processes. The induction of cell elongation in hypocotyls requires temperature sensing in cotyledons, followed by generation of a mobile auxin signal. Subsequently, auxin travels to the hypocotyl where it triggers local brassinosteroid-induced cell elongation in seedling stems, which depends upon a distinct, permissive temperature sensor in the hypocotyl. article_processing_charge: No article_type: original author: - first_name: Julia full_name: Bellstaedt, Julia last_name: Bellstaedt - first_name: Jana full_name: Trenner, Jana last_name: Trenner - first_name: Rebecca full_name: Lippmann, Rebecca last_name: Lippmann - first_name: Yvonne full_name: Poeschl, Yvonne last_name: Poeschl - first_name: Xixi full_name: Zhang, Xixi id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A last_name: Zhang orcid: 0000-0001-7048-4627 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Marcel full_name: Quint, Marcel last_name: Quint - first_name: Carolin full_name: Delker, Carolin last_name: Delker citation: ama: Bellstaedt J, Trenner J, Lippmann R, et al. A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls. Plant Physiology. 2019;180(2):757-766. doi:10.1104/pp.18.01377 apa: Bellstaedt, J., Trenner, J., Lippmann, R., Poeschl, Y., Zhang, X., Friml, J., … Delker, C. (2019). A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls. Plant Physiology. ASPB. https://doi.org/10.1104/pp.18.01377 chicago: Bellstaedt, Julia, Jana Trenner, Rebecca Lippmann, Yvonne Poeschl, Xixi Zhang, Jiří Friml, Marcel Quint, and Carolin Delker. “A Mobile Auxin Signal Connects Temperature Sensing in Cotyledons with Growth Responses in Hypocotyls.” Plant Physiology. ASPB, 2019. https://doi.org/10.1104/pp.18.01377. ieee: J. Bellstaedt et al., “A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls,” Plant Physiology, vol. 180, no. 2. ASPB, pp. 757–766, 2019. ista: Bellstaedt J, Trenner J, Lippmann R, Poeschl Y, Zhang X, Friml J, Quint M, Delker C. 2019. A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls. Plant Physiology. 180(2), 757–766. mla: Bellstaedt, Julia, et al. “A Mobile Auxin Signal Connects Temperature Sensing in Cotyledons with Growth Responses in Hypocotyls.” Plant Physiology, vol. 180, no. 2, ASPB, 2019, pp. 757–66, doi:10.1104/pp.18.01377. short: J. Bellstaedt, J. Trenner, R. Lippmann, Y. Poeschl, X. Zhang, J. Friml, M. Quint, C. Delker, Plant Physiology 180 (2019) 757–766. date_created: 2019-04-30T15:24:22Z date_published: 2019-06-01T00:00:00Z date_updated: 2023-09-05T12:25:19Z day: '01' department: - _id: JiFr doi: 10.1104/pp.18.01377 external_id: isi: - '000470086100019' pmid: - '31000634' intvolume: ' 180' isi: 1 issue: '2' language: - iso: eng main_file_link: - open_access: '1' url: www.doi.org/10.1104/pp.18.01377 month: '06' oa: 1 oa_version: Published Version page: 757-766 pmid: 1 publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: ASPB quality_controlled: '1' scopus_import: '1' status: public title: A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 180 year: '2019' ... --- _id: '6259' abstract: - lang: eng text: The plant hormone auxin has crucial roles in almost all aspects of plant growth and development. Concentrations of auxin vary across different tissues, mediating distinct developmental outcomes and contributing to the functional diversity of auxin. However, the mechanisms that underlie these activities are poorly understood. Here we identify an auxin signalling mechanism, which acts in parallel to the canonical auxin pathway based on the transport inhibitor response1 (TIR1) and other auxin receptor F-box (AFB) family proteins (TIR1/AFB receptors)1,2, that translates levels of cellular auxin to mediate differential growth during apical-hook development. This signalling mechanism operates at the concave side of the apical hook, and involves auxin-mediated C-terminal cleavage of transmembrane kinase 1 (TMK1). The cytosolic and nucleus-translocated C terminus of TMK1 specifically interacts with and phosphorylates two non-canonical transcriptional repressors of the auxin or indole-3-acetic acid (Aux/IAA) family (IAA32 and IAA34), thereby regulating ARF transcription factors. In contrast to the degradation of Aux/IAA transcriptional repressors in the canonical pathway, the newly identified mechanism stabilizes the non-canonical IAA32 and IAA34 transcriptional repressors to regulate gene expression and ultimately inhibit growth. The auxin–TMK1 signalling pathway originates at the cell surface, is triggered by high levels of auxin and shares a partially overlapping set of transcription factors with the TIR1/AFB signalling pathway. This allows distinct interpretations of different concentrations of cellular auxin, and thus enables this versatile signalling molecule to mediate complex developmental outcomes. article_processing_charge: No article_type: original author: - first_name: Min full_name: Cao, Min last_name: Cao - first_name: Rong full_name: Chen, Rong last_name: Chen - first_name: Pan full_name: Li, Pan last_name: Li - first_name: Yongqiang full_name: Yu, Yongqiang last_name: Yu - first_name: Rui full_name: Zheng, Rui last_name: Zheng - first_name: Danfeng full_name: Ge, Danfeng last_name: Ge - first_name: Wei full_name: Zheng, Wei last_name: Zheng - first_name: Xuhui full_name: Wang, Xuhui last_name: Wang - first_name: Yangtao full_name: Gu, Yangtao last_name: Gu - first_name: Zuzana full_name: Gelová, Zuzana id: 0AE74790-0E0B-11E9-ABC7-1ACFE5697425 last_name: Gelová orcid: 0000-0003-4783-1752 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Heng full_name: Zhang, Heng last_name: Zhang - first_name: Renyi full_name: Liu, Renyi last_name: Liu - first_name: Jun full_name: He, Jun last_name: He - first_name: Tongda full_name: Xu, Tongda last_name: Xu citation: ama: Cao M, Chen R, Li P, et al. TMK1-mediated auxin signalling regulates differential growth of the apical hook. Nature. 2019;568:240-243. doi:10.1038/s41586-019-1069-7 apa: Cao, M., Chen, R., Li, P., Yu, Y., Zheng, R., Ge, D., … Xu, T. (2019). TMK1-mediated auxin signalling regulates differential growth of the apical hook. Nature. Springer Nature. https://doi.org/10.1038/s41586-019-1069-7 chicago: Cao, Min, Rong Chen, Pan Li, Yongqiang Yu, Rui Zheng, Danfeng Ge, Wei Zheng, et al. “TMK1-Mediated Auxin Signalling Regulates Differential Growth of the Apical Hook.” Nature. Springer Nature, 2019. https://doi.org/10.1038/s41586-019-1069-7. ieee: M. Cao et al., “TMK1-mediated auxin signalling regulates differential growth of the apical hook,” Nature, vol. 568. Springer Nature, pp. 240–243, 2019. ista: Cao M, Chen R, Li P, Yu Y, Zheng R, Ge D, Zheng W, Wang X, Gu Y, Gelová Z, Friml J, Zhang H, Liu R, He J, Xu T. 2019. TMK1-mediated auxin signalling regulates differential growth of the apical hook. Nature. 568, 240–243. mla: Cao, Min, et al. “TMK1-Mediated Auxin Signalling Regulates Differential Growth of the Apical Hook.” Nature, vol. 568, Springer Nature, 2019, pp. 240–43, doi:10.1038/s41586-019-1069-7. short: M. Cao, R. Chen, P. Li, Y. Yu, R. Zheng, D. Ge, W. Zheng, X. Wang, Y. Gu, Z. Gelová, J. Friml, H. Zhang, R. Liu, J. He, T. Xu, Nature 568 (2019) 240–243. date_created: 2019-04-09T08:37:05Z date_published: 2019-04-11T00:00:00Z date_updated: 2023-09-05T14:58:41Z day: '11' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41586-019-1069-7 ec_funded: 1 external_id: isi: - '000464412700050' pmid: - '30944466' file: - access_level: open_access checksum: 6b84ab602a34382cf0340a37a1378c75 content_type: application/pdf creator: dernst date_created: 2020-11-13T07:37:41Z date_updated: 2020-11-13T07:37:41Z file_id: '8751' file_name: 2019_Nature _Cao_accepted.pdf file_size: 4321328 relation: main_file success: 1 file_date_updated: 2020-11-13T07:37:41Z has_accepted_license: '1' intvolume: ' 568' isi: 1 language: - iso: eng month: '04' oa: 1 oa_version: Submitted Version page: 240-243 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Nature publication_identifier: eissn: - 1476-4687 issn: - 0028-0836 publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/newly-discovered-mechanism-of-plant-hormone-auxin-acts-the-opposite-way/ scopus_import: '1' status: public title: TMK1-mediated auxin signalling regulates differential growth of the apical hook type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 568 year: '2019' ... --- _id: '7106' abstract: - lang: eng text: PIN-FORMED (PIN) transporters mediate directional, intercellular movement of the phytohormone auxin in land plants. To elucidate the evolutionary origins of this developmentally crucial mechanism, we analysed the single PIN homologue of a simple green alga Klebsormidium flaccidum. KfPIN functions as a plasma membrane-localized auxin exporter in land plants and heterologous models. While its role in algae remains unclear, PIN-driven auxin export is probably an ancient and conserved trait within streptophytes. article_processing_charge: No article_type: original author: - first_name: Roman full_name: Skokan, Roman last_name: Skokan - first_name: Eva full_name: Medvecká, Eva last_name: Medvecká - first_name: Tom full_name: Viaene, Tom last_name: Viaene - first_name: Stanislav full_name: Vosolsobě, Stanislav last_name: Vosolsobě - first_name: Marta full_name: Zwiewka, Marta last_name: Zwiewka - first_name: Karel full_name: Müller, Karel last_name: Müller - first_name: Petr full_name: Skůpa, Petr last_name: Skůpa - first_name: Michal full_name: Karady, Michal last_name: Karady - first_name: Yuzhou full_name: Zhang, Yuzhou last_name: Zhang - first_name: Dorina P. full_name: Janacek, Dorina P. last_name: Janacek - first_name: Ulrich Z. full_name: Hammes, Ulrich Z. last_name: Hammes - first_name: Karin full_name: Ljung, Karin last_name: Ljung - first_name: Tomasz full_name: Nodzyński, Tomasz last_name: Nodzyński - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Skokan R, Medvecká E, Viaene T, et al. PIN-driven auxin transport emerged early in streptophyte evolution. Nature Plants. 2019;5(11):1114-1119. doi:10.1038/s41477-019-0542-5 apa: Skokan, R., Medvecká, E., Viaene, T., Vosolsobě, S., Zwiewka, M., Müller, K., … Friml, J. (2019). PIN-driven auxin transport emerged early in streptophyte evolution. Nature Plants. Springer Nature. https://doi.org/10.1038/s41477-019-0542-5 chicago: Skokan, Roman, Eva Medvecká, Tom Viaene, Stanislav Vosolsobě, Marta Zwiewka, Karel Müller, Petr Skůpa, et al. “PIN-Driven Auxin Transport Emerged Early in Streptophyte Evolution.” Nature Plants. Springer Nature, 2019. https://doi.org/10.1038/s41477-019-0542-5. ieee: R. Skokan et al., “PIN-driven auxin transport emerged early in streptophyte evolution,” Nature Plants, vol. 5, no. 11. Springer Nature, pp. 1114–1119, 2019. ista: Skokan R, Medvecká E, Viaene T, Vosolsobě S, Zwiewka M, Müller K, Skůpa P, Karady M, Zhang Y, Janacek DP, Hammes UZ, Ljung K, Nodzyński T, Petrášek J, Friml J. 2019. PIN-driven auxin transport emerged early in streptophyte evolution. Nature Plants. 5(11), 1114–1119. mla: Skokan, Roman, et al. “PIN-Driven Auxin Transport Emerged Early in Streptophyte Evolution.” Nature Plants, vol. 5, no. 11, Springer Nature, 2019, pp. 1114–19, doi:10.1038/s41477-019-0542-5. short: R. Skokan, E. Medvecká, T. Viaene, S. Vosolsobě, M. Zwiewka, K. Müller, P. Skůpa, M. Karady, Y. Zhang, D.P. Janacek, U.Z. Hammes, K. Ljung, T. Nodzyński, J. Petrášek, J. Friml, Nature Plants 5 (2019) 1114–1119. date_created: 2019-11-25T09:08:04Z date_published: 2019-11-01T00:00:00Z date_updated: 2023-09-06T11:09:49Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41477-019-0542-5 ec_funded: 1 external_id: isi: - '000496526100010' pmid: - '31712756' file: - access_level: open_access checksum: 94e0426856aad9a9bd0135d5436efbf1 content_type: application/pdf creator: dernst date_created: 2020-10-14T08:54:49Z date_updated: 2020-10-14T08:54:49Z file_id: '8660' file_name: 2019_NaturePlants_Skokan_accepted.pdf file_size: 1980851 relation: main_file success: 1 file_date_updated: 2020-10-14T08:54:49Z has_accepted_license: '1' intvolume: ' 5' isi: 1 issue: '11' language: - iso: eng month: '11' oa: 1 oa_version: Submitted Version page: 1114-1119 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Nature Plants publication_identifier: issn: - 2055-0278 publication_status: published publisher: Springer Nature quality_controlled: '1' scopus_import: '1' status: public title: PIN-driven auxin transport emerged early in streptophyte evolution type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 5 year: '2019' ... --- _id: '7143' abstract: - lang: eng text: Roots grow downwards parallel to the gravity vector, to anchor a plant in soil and acquire water and nutrients, using a gravitropic mechanism dependent on the asymmetric distribution of the phytohormone auxin. Recently, Chang et al. demonstrate that asymmetric distribution of another phytohormone, cytokinin, directs root growth towards higher water content. article_processing_charge: No article_type: original author: - first_name: Scott A full_name: Sinclair, Scott A id: 2D99FE6A-F248-11E8-B48F-1D18A9856A87 last_name: Sinclair orcid: 0000-0002-4566-0593 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: 'Sinclair SA, Friml J. Defying gravity: a plant’s quest for moisture. Cell Research. 2019;29:965-966. doi:10.1038/s41422-019-0254-4' apa: 'Sinclair, S. A., & Friml, J. (2019). Defying gravity: a plant’s quest for moisture. Cell Research. Springer Nature. https://doi.org/10.1038/s41422-019-0254-4' chicago: 'Sinclair, Scott A, and Jiří Friml. “Defying Gravity: A Plant’s Quest for Moisture.” Cell Research. Springer Nature, 2019. https://doi.org/10.1038/s41422-019-0254-4.' ieee: 'S. A. Sinclair and J. Friml, “Defying gravity: a plant’s quest for moisture,” Cell Research, vol. 29. Springer Nature, pp. 965–966, 2019.' ista: 'Sinclair SA, Friml J. 2019. Defying gravity: a plant’s quest for moisture. Cell Research. 29, 965–966.' mla: 'Sinclair, Scott A., and Jiří Friml. “Defying Gravity: A Plant’s Quest for Moisture.” Cell Research, vol. 29, Springer Nature, 2019, pp. 965–66, doi:10.1038/s41422-019-0254-4.' short: S.A. Sinclair, J. Friml, Cell Research 29 (2019) 965–966. date_created: 2019-12-02T12:30:48Z date_published: 2019-12-01T00:00:00Z date_updated: 2023-09-06T11:20:58Z day: '01' department: - _id: JiFr doi: 10.1038/s41422-019-0254-4 external_id: isi: - '000500749600001' pmid: - '31745287' intvolume: ' 29' isi: 1 language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1038/s41422-019-0254-4 month: '12' oa: 1 oa_version: Published Version page: 965-966 pmid: 1 publication: Cell Research publication_identifier: eissn: - 1748-7838 issn: - 1001-0602 publication_status: published publisher: Springer Nature quality_controlled: '1' scopus_import: '1' status: public title: 'Defying gravity: a plant''s quest for moisture' type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 29 year: '2019' ... --- _id: '7182' abstract: - lang: eng text: During infection pathogens secrete small molecules, termed effectors, to manipulate and control the interaction with their specific hosts. Both the pathogen and the plant are under high selective pressure to rapidly adapt and co-evolve in what is usually referred to as molecular arms race. Components of the host’s immune system form a network that processes information about molecules with a foreign origin and damage-associated signals, integrating them with developmental and abiotic cues to adapt the plant’s responses. Both in the case of nucleotide-binding leucine-rich repeat receptors and leucine-rich repeat receptor kinases interaction networks have been extensively characterized. However, little is known on whether pathogenic effectors form complexes to overcome plant immunity and promote disease. Ustilago maydis, a biotrophic fungal pathogen that infects maize plants, produces effectors that target hubs in the immune network of the host cell. Here we assess the capability of U. maydis effector candidates to interact with each other, which may play a crucial role during the infection process. Using a systematic yeast-two-hybrid approach and based on a preliminary pooled screen, we selected 63 putative effectors for one-on-one matings with a library of nearly 300 effector candidates. We found that 126 of these effector candidates interacted either with themselves or other predicted effectors. Although the functional relevance of the observed interactions remains elusive, we propose that the observed abundance in complex formation between effectors adds an additional level of complexity to effector research and should be taken into consideration when studying effector evolution and function. Based on this fundamental finding, we suggest various scenarios which could evolutionarily drive the formation and stabilization of an effector interactome. article_number: '1437' article_processing_charge: No article_type: original author: - first_name: André full_name: Alcântara, André last_name: Alcântara - first_name: Jason full_name: Bosch, Jason last_name: Bosch - first_name: Fahimeh full_name: Nazari, Fahimeh last_name: Nazari - first_name: Gesa full_name: Hoffmann, Gesa last_name: Hoffmann - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: Simon full_name: Uhse, Simon last_name: Uhse - first_name: Martin A. full_name: Darino, Martin A. last_name: Darino - first_name: Toluwase full_name: Olukayode, Toluwase last_name: Olukayode - first_name: Daniel full_name: Reumann, Daniel last_name: Reumann - first_name: Laura full_name: Baggaley, Laura last_name: Baggaley - first_name: Armin full_name: Djamei, Armin last_name: Djamei citation: ama: Alcântara A, Bosch J, Nazari F, et al. Systematic Y2H screening reveals extensive effector-complex formation. Frontiers in Plant Science. 2019;10(11). doi:10.3389/fpls.2019.01437 apa: Alcântara, A., Bosch, J., Nazari, F., Hoffmann, G., Gallei, M. C., Uhse, S., … Djamei, A. (2019). Systematic Y2H screening reveals extensive effector-complex formation. Frontiers in Plant Science. Frontiers. https://doi.org/10.3389/fpls.2019.01437 chicago: Alcântara, André, Jason Bosch, Fahimeh Nazari, Gesa Hoffmann, Michelle C Gallei, Simon Uhse, Martin A. Darino, et al. “Systematic Y2H Screening Reveals Extensive Effector-Complex Formation.” Frontiers in Plant Science. Frontiers, 2019. https://doi.org/10.3389/fpls.2019.01437. ieee: A. Alcântara et al., “Systematic Y2H screening reveals extensive effector-complex formation,” Frontiers in Plant Science, vol. 10, no. 11. Frontiers, 2019. ista: Alcântara A, Bosch J, Nazari F, Hoffmann G, Gallei MC, Uhse S, Darino MA, Olukayode T, Reumann D, Baggaley L, Djamei A. 2019. Systematic Y2H screening reveals extensive effector-complex formation. Frontiers in Plant Science. 10(11), 1437. mla: Alcântara, André, et al. “Systematic Y2H Screening Reveals Extensive Effector-Complex Formation.” Frontiers in Plant Science, vol. 10, no. 11, 1437, Frontiers, 2019, doi:10.3389/fpls.2019.01437. short: A. Alcântara, J. Bosch, F. Nazari, G. Hoffmann, M.C. Gallei, S. Uhse, M.A. Darino, T. Olukayode, D. Reumann, L. Baggaley, A. Djamei, Frontiers in Plant Science 10 (2019). date_created: 2019-12-15T23:00:43Z date_published: 2019-11-14T00:00:00Z date_updated: 2023-09-06T14:33:46Z day: '14' ddc: - '580' department: - _id: JiFr doi: 10.3389/fpls.2019.01437 external_id: isi: - '000499821700001' pmid: - '31803201' file: - access_level: open_access checksum: 995aa838aec2064d93550de82b40bbd1 content_type: application/pdf creator: dernst date_created: 2019-12-16T07:58:43Z date_updated: 2020-07-14T12:47:52Z file_id: '7185' file_name: 2019_FrontiersPlant_Alcantara.pdf file_size: 1532505 relation: main_file file_date_updated: 2020-07-14T12:47:52Z has_accepted_license: '1' intvolume: ' 10' isi: 1 issue: '11' language: - iso: eng month: '11' oa: 1 oa_version: Published Version pmid: 1 publication: Frontiers in Plant Science publication_identifier: eissn: - 1664462X publication_status: published publisher: Frontiers quality_controlled: '1' scopus_import: '1' status: public title: Systematic Y2H screening reveals extensive effector-complex formation tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 10 year: '2019' ... --- _id: '6377' abstract: - lang: eng text: Clathrin-mediated endocytosis (CME) is a highly conserved and essential cellular process in eukaryotic cells, but its dynamic and vital nature makes it challenging to study using classical genetics tools. In contrast, although small molecules can acutely and reversibly perturb CME, the few chemical CME inhibitors that have been applied to plants are either ineffective or show undesirable side effects. Here, we identify the previously described endosidin9 (ES9) as an inhibitor of clathrin heavy chain (CHC) function in both Arabidopsis and human cells through affinity-based target isolation, in vitro binding studies and X-ray crystallography. Moreover, we present a chemically improved ES9 analog, ES9-17, which lacks the undesirable side effects of ES9 while retaining the ability to target CHC. ES9 and ES9-17 have expanded the chemical toolbox used to probe CHC function, and present chemical scaffolds for further design of more specific and potent CHC inhibitors across different systems. article_processing_charge: No article_type: original author: - first_name: Wim full_name: Dejonghe, Wim last_name: Dejonghe - first_name: Isha full_name: Sharma, Isha last_name: Sharma - first_name: Bram full_name: Denoo, Bram last_name: Denoo - first_name: Steven full_name: De Munck, Steven last_name: De Munck - first_name: Qing full_name: Lu, Qing last_name: Lu - first_name: Kiril full_name: Mishev, Kiril last_name: Mishev - first_name: Haydar full_name: Bulut, Haydar last_name: Bulut - first_name: Evelien full_name: Mylle, Evelien last_name: Mylle - first_name: Riet full_name: De Rycke, Riet last_name: De Rycke - first_name: Mina K full_name: Vasileva, Mina K id: 3407EB18-F248-11E8-B48F-1D18A9856A87 last_name: Vasileva - first_name: Daniel V. full_name: Savatin, Daniel V. last_name: Savatin - first_name: Wim full_name: Nerinckx, Wim last_name: Nerinckx - first_name: An full_name: Staes, An last_name: Staes - first_name: Andrzej full_name: Drozdzecki, Andrzej last_name: Drozdzecki - first_name: Dominique full_name: Audenaert, Dominique last_name: Audenaert - first_name: Klaas full_name: Yperman, Klaas last_name: Yperman - first_name: Annemieke full_name: Madder, Annemieke last_name: Madder - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Daniël full_name: Van Damme, Daniël last_name: Van Damme - first_name: Kris full_name: Gevaert, Kris last_name: Gevaert - first_name: Volker full_name: Haucke, Volker last_name: Haucke - first_name: Savvas N. full_name: Savvides, Savvas N. last_name: Savvides - first_name: Johan full_name: Winne, Johan last_name: Winne - first_name: Eugenia full_name: Russinova, Eugenia last_name: Russinova citation: ama: Dejonghe W, Sharma I, Denoo B, et al. Disruption of endocytosis through chemical inhibition of clathrin heavy chain function. Nature Chemical Biology. 2019;15(6):641–649. doi:10.1038/s41589-019-0262-1 apa: Dejonghe, W., Sharma, I., Denoo, B., De Munck, S., Lu, Q., Mishev, K., … Russinova, E. (2019). Disruption of endocytosis through chemical inhibition of clathrin heavy chain function. Nature Chemical Biology. Springer Nature. https://doi.org/10.1038/s41589-019-0262-1 chicago: Dejonghe, Wim, Isha Sharma, Bram Denoo, Steven De Munck, Qing Lu, Kiril Mishev, Haydar Bulut, et al. “Disruption of Endocytosis through Chemical Inhibition of Clathrin Heavy Chain Function.” Nature Chemical Biology. Springer Nature, 2019. https://doi.org/10.1038/s41589-019-0262-1. ieee: W. Dejonghe et al., “Disruption of endocytosis through chemical inhibition of clathrin heavy chain function,” Nature Chemical Biology, vol. 15, no. 6. Springer Nature, pp. 641–649, 2019. ista: Dejonghe W, Sharma I, Denoo B, De Munck S, Lu Q, Mishev K, Bulut H, Mylle E, De Rycke R, Vasileva MK, Savatin DV, Nerinckx W, Staes A, Drozdzecki A, Audenaert D, Yperman K, Madder A, Friml J, Van Damme D, Gevaert K, Haucke V, Savvides SN, Winne J, Russinova E. 2019. Disruption of endocytosis through chemical inhibition of clathrin heavy chain function. Nature Chemical Biology. 15(6), 641–649. mla: Dejonghe, Wim, et al. “Disruption of Endocytosis through Chemical Inhibition of Clathrin Heavy Chain Function.” Nature Chemical Biology, vol. 15, no. 6, Springer Nature, 2019, pp. 641–649, doi:10.1038/s41589-019-0262-1. short: W. Dejonghe, I. Sharma, B. Denoo, S. De Munck, Q. Lu, K. Mishev, H. Bulut, E. Mylle, R. De Rycke, M.K. Vasileva, D.V. Savatin, W. Nerinckx, A. Staes, A. Drozdzecki, D. Audenaert, K. Yperman, A. Madder, J. Friml, D. Van Damme, K. Gevaert, V. Haucke, S.N. Savvides, J. Winne, E. Russinova, Nature Chemical Biology 15 (2019) 641–649. date_created: 2019-05-05T21:59:11Z date_published: 2019-06-01T00:00:00Z date_updated: 2023-09-07T12:54:35Z day: '01' department: - _id: JiFr doi: 10.1038/s41589-019-0262-1 external_id: isi: - '000468195600018' intvolume: ' 15' isi: 1 issue: '6' language: - iso: eng month: '06' oa_version: None page: 641–649 publication: Nature Chemical Biology publication_identifier: eissn: - '15524469' issn: - '15524450' publication_status: published publisher: Springer Nature quality_controlled: '1' related_material: record: - id: '7172' relation: dissertation_contains status: public scopus_import: '1' status: public title: Disruption of endocytosis through chemical inhibition of clathrin heavy chain function type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 15 year: '2019' ... --- _id: '7172' abstract: - lang: eng text: "The development and growth of Arabidopsis thaliana is regulated by a combination of genetic programing and also by the environmental influences. An important role in these processes play the phytohormones and among them, auxin is crucial as it controls many important functions. It is transported through the whole plant body by creating local and temporal concentration maxima and minima, which have an impact on the cell status, tissue and organ identity. Auxin has the property to undergo a directional and finely regulated cell-to-cell transport, which is enabled by the transport proteins, localized on the plasma membrane. An important role in this process have the PIN auxin efflux proteins, which have an asymmetric/polar subcellular localization and determine the directionality of the auxin transport. During the last years, there were significant advances in understanding how the trafficking molecular machineries function, including studies on molecular interactions, function, subcellular localization and intracellular distribution. However, there is still a lack of detailed characterization on the steps of endocytosis, exocytosis, endocytic recycling and degradation. Due to this fact, I focused on the identification of novel trafficking factors and better characterization of the intracellular trafficking pathways. My PhD thesis consists of an introductory chapter, three experimental chapters, a chapter containing general discussion, conclusions and perspectives and also an appendix chapter with published collaborative papers.\r\nThe first chapter is separated in two different parts: I start by a general introduction to auxin biology and then I introduce the trafficking pathways in the model plant Arabidopsis thaliana. Then, I explain also the phosphorylation-signals for polar targeting and also the roles of the phytohormone strigolactone.\r\nThe second chapter includes the characterization of bar1/sacsin mutant, which was identified in a forward genetic screen for novel trafficking components in Arabidopsis thaliana, where by the implementation of an EMS-treated pPIN1::PIN1-GFP marker line and by using the established inhibitor of ARF-GEFs, Brefeldin A (BFA) as a tool to study trafficking processes, we identified a novel factor, which is mediating the adaptation of the plant cell to ARF-GEF inhibition. The mutation is in a previously uncharacterized gene, encoding a very big protein that we, based on its homologies, called SACSIN with domains suggesting roles as a molecular chaperon or as a component of the ubiquitin-proteasome system. Our physiology and imaging studies revealed that SACSIN is a crucial plant cell component of the adaptation to the ARF-GEF inhibition.\r\nThe third chapter includes six subchapters, where I focus on the role of the phytohormone strigolactone, which interferes with auxin feedback on PIN internalization. Strigolactone moderates the polar auxin transport by increasing the internalization of the PIN auxin efflux carriers, which reduces the canalization related growth responses. In addition, I also studied the role of phosphorylation in the strigolactone regulation of auxin feedback on PIN internalization. In this chapter I also present my results on the MAX2-dependence of strigolactone-mediated root growth inhibition and I also share my results on the auxin metabolomics profiling after application of GR24.\r\nIn the fourth chapter I studied the effect of two small molecules ES-9 and ES9-17, which were identified from a collection of small molecules with the property to impair the clathrin-mediated endocytosis.\r\nIn the fifth chapter, I discuss all my observations and experimental findings and suggest alternative hypothesis to interpret my results.\r\nIn the appendix there are three collaborative published projects. In the first, I participated in the characterization of the role of ES9 as a small molecule, which is inhibitor of clathrin- mediated endocytosis in different model organisms. In the second paper, I contributed to the characterization of another small molecule ES9-17, which is a non-protonophoric analog of ES9 and also impairs the clathrin-mediated endocytosis not only in plant cells, but also in mammalian HeLa cells. Last but not least, I also attach another paper, where I tried to establish the grafting method as a technique in our lab to study canalization related processes." acknowledged_ssus: - _id: LifeSc - _id: Bio alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Mina K full_name: Vasileva, Mina K id: 3407EB18-F248-11E8-B48F-1D18A9856A87 last_name: Vasileva citation: ama: Vasileva MK. Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana. 2019. doi:10.15479/AT:ISTA:7172 apa: Vasileva, M. K. (2019). Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:7172 chicago: Vasileva, Mina K. “Molecular Mechanisms of Endomembrane Trafficking in Arabidopsis Thaliana.” Institute of Science and Technology Austria, 2019. https://doi.org/10.15479/AT:ISTA:7172. ieee: M. K. Vasileva, “Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana,” Institute of Science and Technology Austria, 2019. ista: Vasileva MK. 2019. Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana. Institute of Science and Technology Austria. mla: Vasileva, Mina K. Molecular Mechanisms of Endomembrane Trafficking in Arabidopsis Thaliana. Institute of Science and Technology Austria, 2019, doi:10.15479/AT:ISTA:7172. short: M.K. Vasileva, Molecular Mechanisms of Endomembrane Trafficking in Arabidopsis Thaliana, Institute of Science and Technology Austria, 2019. date_created: 2019-12-11T21:24:39Z date_published: 2019-12-12T00:00:00Z date_updated: 2023-09-19T10:39:33Z day: '12' ddc: - '570' degree_awarded: PhD department: - _id: JiFr doi: 10.15479/AT:ISTA:7172 file: - access_level: closed checksum: ef981c1a3b1d9da0edcbedcff4970d37 content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: mvasilev date_created: 2019-12-12T09:32:36Z date_updated: 2020-07-14T12:47:51Z file_id: '7175' file_name: Thesis_Mina_final_upload_7.docx file_size: 20454014 relation: source_file - access_level: open_access checksum: 3882c4585e46c9cfb486e4225cad54ab content_type: application/pdf creator: mvasilev date_created: 2019-12-12T09:33:10Z date_updated: 2020-07-14T12:47:51Z file_id: '7176' file_name: Thesis_Mina_final_upload_7.pdf file_size: 11565025 relation: main_file file_date_updated: 2020-07-14T12:47:51Z has_accepted_license: '1' language: - iso: eng month: '12' oa: 1 oa_version: Published Version page: '192' publication_identifier: eissn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '1346' relation: part_of_dissertation status: public - id: '6377' relation: part_of_dissertation status: public - id: '449' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2019' ... --- _id: '6999' abstract: - lang: eng text: Plasmodesmata (PD) are plant-specific membrane-lined channels that create cytoplasmic and membrane continuities between adjacent cells, thereby facilitating cell–cell communication and virus movement. Plant cells have evolved diverse mechanisms to regulate PD plasticity in response to numerous environmental stimuli. In particular, during defense against plant pathogens, the defense hormone, salicylic acid (SA), plays a crucial role in the regulation of PD permeability in a callose-dependent manner. Here, we uncover a mechanism by which plants restrict the spreading of virus and PD cargoes using SA signaling by increasing lipid order and closure of PD. We showed that exogenous SA application triggered the compartmentalization of lipid raft nanodomains through a modulation of the lipid raft-regulatory protein, Remorin (REM). Genetic studies, superresolution imaging, and transmission electron microscopy observation together demonstrated that Arabidopsis REM1.2 and REM1.3 are crucial for plasma membrane nanodomain assembly to control PD aperture and functionality. In addition, we also found that a 14-3-3 epsilon protein modulates REM clustering and membrane nanodomain compartmentalization through its direct interaction with REM proteins. This study unveils a molecular mechanism by which the key plant defense hormone, SA, triggers membrane lipid nanodomain reorganization, thereby regulating PD closure to impede virus spreading. article_processing_charge: No article_type: original author: - first_name: D full_name: Huang, D last_name: Huang - first_name: Y full_name: Sun, Y last_name: Sun - first_name: Z full_name: Ma, Z last_name: Ma - first_name: M full_name: Ke, M last_name: Ke - first_name: Y full_name: Cui, Y last_name: Cui - first_name: Z full_name: Chen, Z last_name: Chen - first_name: C full_name: Chen, C last_name: Chen - first_name: C full_name: Ji, C last_name: Ji - first_name: TM full_name: Tran, TM last_name: Tran - first_name: L full_name: Yang, L last_name: Yang - first_name: SM full_name: Lam, SM last_name: Lam - first_name: Y full_name: Han, Y last_name: Han - first_name: G full_name: Shu, G last_name: Shu - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Y full_name: Miao, Y last_name: Miao - first_name: L full_name: Jiang, L last_name: Jiang - first_name: X full_name: Chen, X last_name: Chen citation: ama: Huang D, Sun Y, Ma Z, et al. Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization. Proceedings of the National Academy of Sciences of the United States of America. 2019;116(42):21274-21284. doi:10.1073/pnas.1911892116 apa: Huang, D., Sun, Y., Ma, Z., Ke, M., Cui, Y., Chen, Z., … Chen, X. (2019). Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization. Proceedings of the National Academy of Sciences of the United States of America. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1911892116 chicago: Huang, D, Y Sun, Z Ma, M Ke, Y Cui, Z Chen, C Chen, et al. “Salicylic Acid-Mediated Plasmodesmal Closure via Remorin-Dependent Lipid Organization.” Proceedings of the National Academy of Sciences of the United States of America. Proceedings of the National Academy of Sciences, 2019. https://doi.org/10.1073/pnas.1911892116. ieee: D. Huang et al., “Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization,” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 42. Proceedings of the National Academy of Sciences, pp. 21274–21284, 2019. ista: Huang D, Sun Y, Ma Z, Ke M, Cui Y, Chen Z, Chen C, Ji C, Tran T, Yang L, Lam S, Han Y, Shu G, Friml J, Miao Y, Jiang L, Chen X. 2019. Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization. Proceedings of the National Academy of Sciences of the United States of America. 116(42), 21274–21284. mla: Huang, D., et al. “Salicylic Acid-Mediated Plasmodesmal Closure via Remorin-Dependent Lipid Organization.” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 42, Proceedings of the National Academy of Sciences, 2019, pp. 21274–84, doi:10.1073/pnas.1911892116. short: D. Huang, Y. Sun, Z. Ma, M. Ke, Y. Cui, Z. Chen, C. Chen, C. Ji, T. Tran, L. Yang, S. Lam, Y. Han, G. Shu, J. Friml, Y. Miao, L. Jiang, X. Chen, Proceedings of the National Academy of Sciences of the United States of America 116 (2019) 21274–21284. date_created: 2019-11-12T11:42:05Z date_published: 2019-10-15T00:00:00Z date_updated: 2023-10-17T12:32:37Z day: '15' ddc: - '580' department: - _id: JiFr doi: 10.1073/pnas.1911892116 external_id: isi: - '000490183000068' pmid: - '31575745' file: - access_level: open_access checksum: 258c666bc6253eab81961f61169eefae content_type: application/pdf creator: dernst date_created: 2019-11-13T08:22:28Z date_updated: 2020-07-14T12:47:46Z file_id: '7012' file_name: 2019_PNAS_Huang.pdf file_size: 3287466 relation: main_file file_date_updated: 2020-07-14T12:47:46Z has_accepted_license: '1' intvolume: ' 116' isi: 1 issue: '42' language: - iso: eng month: '10' oa: 1 oa_version: Published Version page: 21274-21284 pmid: 1 publication: Proceedings of the National Academy of Sciences of the United States of America publication_identifier: eissn: - 1091-6490 issn: - 0027-8424 publication_status: published publisher: Proceedings of the National Academy of Sciences quality_controlled: '1' related_material: link: - relation: erratum url: https://doi.org/10.1073/pnas.2004738117 scopus_import: '1' status: public title: Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 116 year: '2019' ... --- _id: '6269' abstract: - lang: eng text: 'Clathrin-Mediated Endocytosis (CME) is an aspect of cellular trafficking that is constantly regulated for mediating developmental and physiological responses. The main aim of my thesis is to decipher the basic mechanisms of CME and post-endocytic trafficking in the whole multicellular organ systems of Arabidopsis. The first chapter of my thesis describes the search for new components involved in CME. Tandem affinity purification was conducted using CLC and its interacting partners were identified. Amongst the identified proteins were the Auxilin-likes1 and 2 (Axl1/2), putative uncoating factors, for which we made a full functional analysis. Over-expression of Axl1/2 causes extreme modifications in the dynamics of the machinery proteins and inhibition of endocytosis altogether. However the loss of function of the axl1/2 did not present any cellular or physiological phenotype, meaning Auxilin-likes do not form the major uncoating machinery. The second chapter of my thesis describes the establishment/utilisation of techniques to capture the dynamicity and the complexity of CME and post-endocytic trafficking. We have studied the development of endocytic pits at the PM – specifically, the mode of membrane remodeling during pit development and the role of actin in it, given plant cells possess high turgor pressure. Utilizing the improved z-resolution of TIRF and VAEM techniques, we captured the time-lapse of the endocytic events at the plasma membrane; and using particle detection software, we quantitatively analysed all the endocytic trajectories in an unbiased way to obtain the endocytic rate of the system. This together with the direct analysis of cargo internalisation from the PM provided an estimate on the endocytic potential of the cell. We also developed a methodology for ultrastructural analysis of different populations of Clathrin-Coated Structures (CCSs) in both PM and endomembranes in unroofed protoplasts. Structural analysis, together with the intensity profile of CCSs at the PM show that the mode of CCP development at the PM follows ‘Constant curvature model’; meaning that clathrin polymerisation energy is a major contributing factor of membrane remodeling. In addition, other analyses clearly show that actin is not required for membrane remodeling during invagination or any other step of CCP development, despite the prevalent high turgor pressure. However, actin is essential in orchestrating the post-endocytic trafficking of CCVs facilitating the EE formation. We also observed that the uncoating process post-endocytosis is not immediate; an alternative mechanism of uncoating – Sequential multi-step process – functions in the cell. Finally we also looked at one of the important physiological stimuli modulating the process – hormone, auxin. auxin has been known to influence CME before. We have made a detailed study on the concentration-time based effect of auxin on the machinery proteins, CCP development, and the specificity of cargoes endocytosed. To this end, we saw no general effect of auxin on CME at earlier time points. However, very low concentration of IAA, such as 50nM, accelerates endocytosis of specifically PIN2 through CME. Such a tight regulatory control with high specificity to PIN2 could be essential in modulating its polarity. ' acknowledged_ssus: - _id: Bio - _id: EM-Fac alternative_title: - ISTA Thesis article_processing_charge: No author: - first_name: Madhumitha full_name: Narasimhan, Madhumitha id: 44BF24D0-F248-11E8-B48F-1D18A9856A87 last_name: Narasimhan orcid: 0000-0002-8600-0671 citation: ama: Narasimhan M. Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants . 2019. doi:10.15479/at:ista:th1075 apa: Narasimhan, M. (2019). Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants . Institute of Science and Technology Austria. https://doi.org/10.15479/at:ista:th1075 chicago: Narasimhan, Madhumitha. “Clathrin-Mediated Endocytosis, Post-Endocytic Trafficking and Their Regulatory Controls in Plants .” Institute of Science and Technology Austria, 2019. https://doi.org/10.15479/at:ista:th1075. ieee: M. Narasimhan, “Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants ,” Institute of Science and Technology Austria, 2019. ista: Narasimhan M. 2019. Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants . Institute of Science and Technology Austria. mla: Narasimhan, Madhumitha. Clathrin-Mediated Endocytosis, Post-Endocytic Trafficking and Their Regulatory Controls in Plants . Institute of Science and Technology Austria, 2019, doi:10.15479/at:ista:th1075. short: M. Narasimhan, Clathrin-Mediated Endocytosis, Post-Endocytic Trafficking and Their Regulatory Controls in Plants , Institute of Science and Technology Austria, 2019. date_created: 2019-04-09T14:37:06Z date_published: 2019-02-04T00:00:00Z date_updated: 2023-09-08T11:43:03Z day: '04' ddc: - '575' degree_awarded: PhD department: - _id: JiFr doi: 10.15479/at:ista:th1075 file: - access_level: open_access checksum: c958f27dd752712886e7e2638b847a3c content_type: video/x-msvideo creator: dernst date_created: 2019-04-09T14:35:18Z date_updated: 2021-02-11T23:30:15Z embargo: 2020-02-11 file_id: '6270' file_name: Supplementary_movie_1.avi file_size: 5402078 relation: main_file - access_level: open_access checksum: 8786fdc29c62987c0aad3c866a4d3691 content_type: video/x-msvideo creator: dernst date_created: 2019-04-09T14:35:18Z date_updated: 2021-02-11T23:30:15Z embargo: 2020-02-11 file_id: '6271' file_name: 3.7_supplementary_movie_10.avi file_size: 5927736 relation: main_file - access_level: open_access checksum: 25f784c5159d6f4d966b2f9b371ebaf6 content_type: video/x-msvideo creator: dernst date_created: 2019-04-09T14:35:18Z date_updated: 2021-02-11T23:30:15Z embargo: 2020-02-11 file_id: '6272' file_name: 3.7_supplementary_movie_9.avi file_size: 9570210 relation: main_file - 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access_level: open_access checksum: 4fcdaa3a6c645514a3b3205f0f69dc76 content_type: application/pdf creator: dernst date_created: 2019-04-09T14:35:33Z date_updated: 2021-02-11T11:17:15Z embargo: 2020-02-11 file_id: '6285' file_name: 2019_Thesis_Narasimhan.pdf file_size: 10553937 relation: main_file - access_level: closed checksum: 268f0b6bad21d5f0d671e5d4b88104a7 content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document creator: dernst date_created: 2019-04-09T14:35:36Z date_updated: 2020-07-14T12:47:26Z embargo_to: open_access file_id: '6286' file_name: 2019_Thesis_Narasimhan_source.docx file_size: 135291990 relation: source_file file_date_updated: 2021-02-11T23:30:15Z has_accepted_license: '1' language: - iso: eng month: '02' oa: 1 oa_version: Published Version page: '138' publication_identifier: issn: - 2663-337X publication_status: published publisher: Institute of Science and Technology Austria related_material: record: - id: '412' relation: part_of_dissertation status: public status: public supervisor: - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 title: 'Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants ' tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: dissertation user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2019' ... --- _id: '6351' abstract: - lang: eng text: "A process of restorative patterning in plant roots correctly replaces eliminated cells to heal local injuries despite the absence of cell migration, which underpins wound healing in animals. \r\n\r\nPatterning in plants relies on oriented cell divisions and acquisition of specific cell identities. Plants regularly endure wounds caused by abiotic or biotic environmental stimuli and have developed extraordinary abilities to restore their tissues after injuries. Here, we provide insight into a mechanism of restorative patterning that repairs tissues after wounding. Laser-assisted elimination of different cells in Arabidopsis root combined with live-imaging tracking during vertical growth allowed analysis of the regeneration processes in vivo. Specifically, the cells adjacent to the inner side of the injury re-activated their stem cell transcriptional programs. They accelerated their progression through cell cycle, coordinately changed the cell division orientation, and ultimately acquired de novo the correct cell fates to replace missing cells. These observations highlight existence of unknown intercellular positional signaling and demonstrate the capability of specified cells to re-acquire stem cell programs as a crucial part of the plant-specific mechanism of wound healing." acknowledged_ssus: - _id: Bio article_processing_charge: No author: - first_name: Petra full_name: Marhavá, Petra id: 44E59624-F248-11E8-B48F-1D18A9856A87 last_name: Marhavá - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 - first_name: Saiko full_name: Yoshida, Saiko id: 2E46069C-F248-11E8-B48F-1D18A9856A87 last_name: Yoshida - first_name: Peter full_name: Marhavy, Peter id: 3F45B078-F248-11E8-B48F-1D18A9856A87 last_name: Marhavy orcid: 0000-0001-5227-5741 - first_name: Eva full_name: Benková, Eva id: 38F4F166-F248-11E8-B48F-1D18A9856A87 last_name: Benková orcid: 0000-0002-8510-9739 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Marhavá P, Hörmayer L, Yoshida S, Marhavý P, Benková E, Friml J. Re-activation of stem cell pathways for pattern restoration in plant wound healing. Cell. 2019;177(4):957-969.e13. doi:10.1016/j.cell.2019.04.015 apa: Marhavá, P., Hörmayer, L., Yoshida, S., Marhavý, P., Benková, E., & Friml, J. (2019). Re-activation of stem cell pathways for pattern restoration in plant wound healing. Cell. Elsevier. https://doi.org/10.1016/j.cell.2019.04.015 chicago: Marhavá, Petra, Lukas Hörmayer, Saiko Yoshida, Peter Marhavý, Eva Benková, and Jiří Friml. “Re-Activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing.” Cell. Elsevier, 2019. https://doi.org/10.1016/j.cell.2019.04.015. ieee: P. Marhavá, L. Hörmayer, S. Yoshida, P. Marhavý, E. Benková, and J. Friml, “Re-activation of stem cell pathways for pattern restoration in plant wound healing,” Cell, vol. 177, no. 4. Elsevier, p. 957–969.e13, 2019. ista: Marhavá P, Hörmayer L, Yoshida S, Marhavý P, Benková E, Friml J. 2019. Re-activation of stem cell pathways for pattern restoration in plant wound healing. Cell. 177(4), 957–969.e13. mla: Marhavá, Petra, et al. “Re-Activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing.” Cell, vol. 177, no. 4, Elsevier, 2019, p. 957–969.e13, doi:10.1016/j.cell.2019.04.015. short: P. Marhavá, L. Hörmayer, S. Yoshida, P. Marhavý, E. Benková, J. Friml, Cell 177 (2019) 957–969.e13. date_created: 2019-04-28T21:59:14Z date_published: 2019-05-02T00:00:00Z date_updated: 2024-03-27T23:30:10Z day: '02' ddc: - '570' department: - _id: JiFr - _id: EvBe doi: 10.1016/j.cell.2019.04.015 ec_funded: 1 external_id: isi: - '000466843000015' pmid: - '31051107' file: - access_level: open_access checksum: 4ceba04a96a74f5092ec3ce2c579a0c7 content_type: application/pdf creator: dernst date_created: 2019-05-13T06:12:45Z date_updated: 2020-07-14T12:47:28Z file_id: '6411' file_name: 2019_Cell_Marhava.pdf file_size: 10272032 relation: main_file file_date_updated: 2020-07-14T12:47:28Z has_accepted_license: '1' intvolume: ' 177' isi: 1 issue: '4' language: - iso: eng month: '05' oa: 1 oa_version: Published Version page: 957-969.e13 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Cell publication_identifier: eissn: - '10974172' issn: - '00928674' publication_status: published publisher: Elsevier quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/specialized-plant-cells-regain-stem-cell-features-to-heal-wounds/ record: - id: '9992' relation: dissertation_contains status: public scopus_import: '1' status: public title: Re-activation of stem cell pathways for pattern restoration in plant wound healing tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 177 year: '2019' ... --- _id: '6943' abstract: - lang: eng text: Plants as sessile organisms are constantly under attack by herbivores, rough environmental situations, or mechanical pressure. These challenges often lead to the induction of wounds or destruction of already specified and developed tissues. Additionally, wounding makes plants vulnerable to invasion by pathogens, which is why wound signalling often triggers specific defence responses. To stay competitive or, eventually, survive under these circumstances, plants need to regenerate efficiently, which in rigid, tissue migration-incompatible plant tissues requires post-embryonic patterning and organogenesis. Now, several studies used laser-assisted single cell ablation in the Arabidopsis root tip as a minimal wounding proxy. Here, we discuss their findings and put them into context of a broader spectrum of wound signalling, pathogen responses and tissue as well as organ regeneration. article_processing_charge: No article_type: original author: - first_name: Lukas full_name: Hörmayer, Lukas id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87 last_name: Hörmayer orcid: 0000-0001-8295-2926 - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Hörmayer L, Friml J. Targeted cell ablation-based insights into wound healing and restorative patterning. Current Opinion in Plant Biology. 2019;52:124-130. doi:10.1016/j.pbi.2019.08.006 apa: Hörmayer, L., & Friml, J. (2019). Targeted cell ablation-based insights into wound healing and restorative patterning. Current Opinion in Plant Biology. Elsevier. https://doi.org/10.1016/j.pbi.2019.08.006 chicago: Hörmayer, Lukas, and Jiří Friml. “Targeted Cell Ablation-Based Insights into Wound Healing and Restorative Patterning.” Current Opinion in Plant Biology. Elsevier, 2019. https://doi.org/10.1016/j.pbi.2019.08.006. ieee: L. Hörmayer and J. Friml, “Targeted cell ablation-based insights into wound healing and restorative patterning,” Current Opinion in Plant Biology, vol. 52. Elsevier, pp. 124–130, 2019. ista: Hörmayer L, Friml J. 2019. Targeted cell ablation-based insights into wound healing and restorative patterning. Current Opinion in Plant Biology. 52, 124–130. mla: Hörmayer, Lukas, and Jiří Friml. “Targeted Cell Ablation-Based Insights into Wound Healing and Restorative Patterning.” Current Opinion in Plant Biology, vol. 52, Elsevier, 2019, pp. 124–30, doi:10.1016/j.pbi.2019.08.006. short: L. Hörmayer, J. Friml, Current Opinion in Plant Biology 52 (2019) 124–130. date_created: 2019-10-14T07:00:24Z date_published: 2019-12-01T00:00:00Z date_updated: 2024-03-27T23:30:11Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1016/j.pbi.2019.08.006 ec_funded: 1 external_id: isi: - '000502890600017' pmid: - '31585333' file: - access_level: open_access checksum: d6fd68a6e965f1efe3f0bf2d2070a616 content_type: application/pdf creator: dernst date_created: 2019-10-14T14:48:21Z date_updated: 2020-07-14T12:47:45Z file_id: '6946' file_name: 2019_CurrentOpinionPlant_Hoermayer.pdf file_size: 1659288 relation: main_file file_date_updated: 2020-07-14T12:47:45Z has_accepted_license: '1' intvolume: ' 52' isi: 1 language: - iso: eng month: '12' oa: 1 oa_version: Published Version page: 124-130 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Current Opinion in Plant Biology publication_identifier: issn: - 1369-5266 publication_status: published publisher: Elsevier quality_controlled: '1' related_material: record: - id: '9992' relation: dissertation_contains status: public scopus_import: '1' status: public title: Targeted cell ablation-based insights into wound healing and restorative patterning tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 52 year: '2019' ... --- _id: '6260' abstract: - lang: eng text: Polar auxin transport plays a pivotal role in plant growth and development. PIN auxin efflux carriers regulate directional auxin movement by establishing local auxin maxima, minima, and gradients that drive multiple developmental processes and responses to environmental signals. Auxin has been proposed to modulate its own transport by regulating subcellular PIN trafficking via processes such as clathrin-mediated PIN endocytosis and constitutive recycling. Here, we further investigated the mechanisms by which auxin affects PIN trafficking by screening auxin analogs and identified pinstatic acid (PISA) as a positive modulator of polar auxin transport in Arabidopsis thaliana. PISA had an auxin-like effect on hypocotyl elongation and adventitious root formation via positive regulation of auxin transport. PISA did not activate SCFTIR1/AFB signaling and yet induced PIN accumulation at the cell surface by inhibiting PIN internalization from the plasma membrane. This work demonstrates PISA to be a promising chemical tool to dissect the regulatory mechanisms behind subcellular PIN trafficking and auxin transport. acknowledgement: "We thank Dr. H. Fukaki (University of Kobe), Dr. R. Offringa (Leiden University), Dr. Jianwei Pan (Zhejiang Normal University), and Dr. M. Estelle (University of California at San Diego) for providing mutants and transgenic line seeds.\r\nThis work was supported by the Ministry of Education, Culture, Sports, Science, and Technology (Grant-in-Aid for Scientific Research no. JP25114518 to K.H.), the Biotechnology and Biological Sciences Research Council (award no. BB/L009366/1 to R.N. and S.K.), and the European Union’s Horizon2020 program (European Research Council grant agreement no. 742985 to J.F.)." article_processing_charge: No article_type: original author: - first_name: A full_name: Oochi, A last_name: Oochi - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: K full_name: Fukui, K last_name: Fukui - first_name: Y full_name: Nakao, Y last_name: Nakao - first_name: Michelle C full_name: Gallei, Michelle C id: 35A03822-F248-11E8-B48F-1D18A9856A87 last_name: Gallei orcid: 0000-0003-1286-7368 - first_name: M full_name: Quareshy, M last_name: Quareshy - first_name: K full_name: Takahashi, K last_name: Takahashi - first_name: T full_name: Kinoshita, T last_name: Kinoshita - first_name: SR full_name: Harborough, SR last_name: Harborough - first_name: S full_name: Kepinski, S last_name: Kepinski - first_name: H full_name: Kasahara, H last_name: Kasahara - first_name: RM full_name: Napier, RM last_name: Napier - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: KI full_name: Hayashi, KI last_name: Hayashi citation: ama: Oochi A, Hajny J, Fukui K, et al. Pinstatic acid promotes auxin transport by inhibiting PIN internalization. Plant Physiology. 2019;180(2):1152-1165. doi:10.1104/pp.19.00201 apa: Oochi, A., Hajny, J., Fukui, K., Nakao, Y., Gallei, M. C., Quareshy, M., … Hayashi, K. (2019). Pinstatic acid promotes auxin transport by inhibiting PIN internalization. Plant Physiology. ASPB. https://doi.org/10.1104/pp.19.00201 chicago: Oochi, A, Jakub Hajny, K Fukui, Y Nakao, Michelle C Gallei, M Quareshy, K Takahashi, et al. “Pinstatic Acid Promotes Auxin Transport by Inhibiting PIN Internalization.” Plant Physiology. ASPB, 2019. https://doi.org/10.1104/pp.19.00201. ieee: A. Oochi et al., “Pinstatic acid promotes auxin transport by inhibiting PIN internalization,” Plant Physiology, vol. 180, no. 2. ASPB, pp. 1152–1165, 2019. ista: Oochi A, Hajny J, Fukui K, Nakao Y, Gallei MC, Quareshy M, Takahashi K, Kinoshita T, Harborough S, Kepinski S, Kasahara H, Napier R, Friml J, Hayashi K. 2019. Pinstatic acid promotes auxin transport by inhibiting PIN internalization. Plant Physiology. 180(2), 1152–1165. mla: Oochi, A., et al. “Pinstatic Acid Promotes Auxin Transport by Inhibiting PIN Internalization.” Plant Physiology, vol. 180, no. 2, ASPB, 2019, pp. 1152–65, doi:10.1104/pp.19.00201. short: A. Oochi, J. Hajny, K. Fukui, Y. Nakao, M.C. Gallei, M. Quareshy, K. Takahashi, T. Kinoshita, S. Harborough, S. Kepinski, H. Kasahara, R. Napier, J. Friml, K. Hayashi, Plant Physiology 180 (2019) 1152–1165. date_created: 2019-04-09T08:38:20Z date_published: 2019-06-01T00:00:00Z date_updated: 2024-03-27T23:30:37Z day: '01' department: - _id: JiFr doi: 10.1104/pp.19.00201 ec_funded: 1 external_id: isi: - '000470086100045' pmid: - '30936248' intvolume: ' 180' isi: 1 issue: '2' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1104/pp.19.00201 month: '06' oa: 1 oa_version: Published Version page: 1152-1165 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Plant Physiology publication_identifier: eissn: - 1532-2548 issn: - 0032-0889 publication_status: published publisher: ASPB quality_controlled: '1' related_material: record: - id: '11626' relation: dissertation_contains status: public - id: '8822' relation: dissertation_contains status: public scopus_import: '1' status: public title: Pinstatic acid promotes auxin transport by inhibiting PIN internalization type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 180 year: '2019' ... --- _id: '6627' abstract: - lang: eng text: Cortical microtubule arrays in elongating epidermal cells in both the root and stem of plants have the propensity of dynamic reorientations that are correlated with the activation or inhibition of growth. Factors regulating plant growth, among them the hormone auxin, have been recognized as regulators of microtubule array orientations. Some previous work in the field has aimed at elucidating the causal relationship between cell growth, the signaling of auxin or other growth-regulating factors, and microtubule array reorientations, with various conclusions. Here, we revisit this problem of causality with a comprehensive set of experiments in Arabidopsis thaliana, using the now available pharmacological and genetic tools. We use isolated, auxin-depleted hypocotyls, an experimental system allowing for full control of both growth and auxin signaling. We demonstrate that reorientation of microtubules is not directly triggered by an auxin signal during growth activation. Instead, reorientation is triggered by the activation of the growth process itself and is auxin-independent in its nature. We discuss these findings in the context of previous relevant work, including that on the mechanical regulation of microtubule array orientation. article_number: '3337' article_processing_charge: Yes article_type: original author: - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Adamowski M, Li L, Friml J. Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling. International Journal of Molecular Sciences. 2019;20(13). doi:10.3390/ijms20133337 apa: Adamowski, M., Li, L., & Friml, J. (2019). Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling. International Journal of Molecular Sciences. MDPI. https://doi.org/10.3390/ijms20133337 chicago: Adamowski, Maciek, Lanxin Li, and Jiří Friml. “Reorientation of Cortical Microtubule Arrays in the Hypocotyl of Arabidopsis Thaliana Is Induced by the Cell Growth Process and Independent of Auxin Signaling.” International Journal of Molecular Sciences. MDPI, 2019. https://doi.org/10.3390/ijms20133337. ieee: M. Adamowski, L. Li, and J. Friml, “Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling,” International Journal of Molecular Sciences, vol. 20, no. 13. MDPI, 2019. ista: Adamowski M, Li L, Friml J. 2019. Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling. International Journal of Molecular Sciences. 20(13), 3337. mla: Adamowski, Maciek, et al. “Reorientation of Cortical Microtubule Arrays in the Hypocotyl of Arabidopsis Thaliana Is Induced by the Cell Growth Process and Independent of Auxin Signaling.” International Journal of Molecular Sciences, vol. 20, no. 13, 3337, MDPI, 2019, doi:10.3390/ijms20133337. short: M. Adamowski, L. Li, J. Friml, International Journal of Molecular Sciences 20 (2019). date_created: 2019-07-11T12:00:32Z date_published: 2019-07-07T00:00:00Z date_updated: 2024-03-27T23:30:43Z day: '07' ddc: - '580' department: - _id: JiFr doi: 10.3390/ijms20133337 ec_funded: 1 external_id: isi: - '000477041100221' pmid: - '31284661' file: - access_level: open_access checksum: dd9d1cbb933a72ceb666c9667890ac51 content_type: application/pdf creator: dernst date_created: 2019-07-17T06:17:15Z date_updated: 2020-07-14T12:47:34Z file_id: '6645' file_name: 2019_JournalMolecularScience_Adamowski.pdf file_size: 3330291 relation: main_file file_date_updated: 2020-07-14T12:47:34Z has_accepted_license: '1' intvolume: ' 20' isi: 1 issue: '13' language: - iso: eng month: '07' oa: 1 oa_version: Published Version pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program - _id: B67AFEDC-15C9-11EA-A837-991A96BB2854 name: IST Austria Open Access Fund publication: International Journal of Molecular Sciences publication_identifier: eissn: - 1422-0067 publication_status: published publisher: MDPI quality_controlled: '1' related_material: record: - id: '10083' relation: dissertation_contains status: public scopus_import: '1' status: public title: Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8 volume: 20 year: '2019' ... --- _id: '408' abstract: - lang: eng text: Adventitious roots (AR) are de novo formed roots that emerge from any part of the plant or from callus in tissue culture, except root tissue. The plant tissue origin and the method by which they are induced determine the physiological properties of emerged ARs. Hence, a standard method encompassing all types of AR does not exist. Here we describe a method for the induction and analysis of AR that emerge from the etiolated hypocotyl of dicot plants. The hypocotyl is formed during embryogenesis and shows a determined developmental pattern which usually does not involve AR formation. However, the hypocotyl shows propensity to form de novo roots under specific circumstances such as removal of the root system, high humidity or flooding, or during de-etiolation. The hypocotyl AR emerge from a pericycle-like cell layer surrounding the vascular tissue of the central cylinder, which is reminiscent to the developmental program of lateral roots. Here we propose an easy protocol for in vitro hypocotyl AR induction from etiolated Arabidopsis seedlings. alternative_title: - MIMB article_processing_charge: No author: - first_name: Hoang full_name: Trinh, Hoang last_name: Trinh - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Danny full_name: Geelen, Danny last_name: Geelen citation: ama: 'Trinh H, Verstraeten I, Geelen D. In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls. In: Root Development . Vol 1761. Springer Nature; 2018:95-102. doi:10.1007/978-1-4939-7747-5_7' apa: Trinh, H., Verstraeten, I., & Geelen, D. (2018). In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls. In Root Development (Vol. 1761, pp. 95–102). Springer Nature. https://doi.org/10.1007/978-1-4939-7747-5_7 chicago: Trinh, Hoang, Inge Verstraeten, and Danny Geelen. “In Vitro Assay for Induction of Adventitious Rooting on Intact Arabidopsis Hypocotyls.” In Root Development , 1761:95–102. Springer Nature, 2018. https://doi.org/10.1007/978-1-4939-7747-5_7. ieee: H. Trinh, I. Verstraeten, and D. Geelen, “In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls,” in Root Development , vol. 1761, Springer Nature, 2018, pp. 95–102. ista: 'Trinh H, Verstraeten I, Geelen D. 2018.In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls. In: Root Development . MIMB, vol. 1761, 95–102.' mla: Trinh, Hoang, et al. “In Vitro Assay for Induction of Adventitious Rooting on Intact Arabidopsis Hypocotyls.” Root Development , vol. 1761, Springer Nature, 2018, pp. 95–102, doi:10.1007/978-1-4939-7747-5_7. short: H. Trinh, I. Verstraeten, D. Geelen, in:, Root Development , Springer Nature, 2018, pp. 95–102. date_created: 2018-12-11T11:46:18Z date_published: 2018-03-01T00:00:00Z date_updated: 2021-01-12T07:54:21Z day: '01' department: - _id: JiFr doi: 10.1007/978-1-4939-7747-5_7 external_id: pmid: - '29525951' intvolume: ' 1761' language: - iso: eng month: '03' oa_version: None page: 95 - 102 pmid: 1 publication: 'Root Development ' publication_identifier: issn: - 1064-3745 publication_status: published publisher: Springer Nature publist_id: '7421' quality_controlled: '1' scopus_import: '1' status: public title: In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls type: book_chapter user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 1761 year: '2018' ... --- _id: '411' abstract: - lang: eng text: Immunolocalization is a valuable tool for cell biology research that allows to rapidly determine the localization and expression levels of endogenous proteins. In plants, whole-mount in situ immunolocalization remains a challenging method, especially in tissues protected by waxy layers and complex cell wall carbohydrates. Here, we present a robust method for whole-mount in situ immunolocalization in primary root meristems and lateral root primordia in Arabidopsis thaliana. For good epitope preservation, fixation is done in an alkaline paraformaldehyde/glutaraldehyde mixture. This fixative is suitable for detecting a wide range of proteins, including integral transmembrane proteins and proteins peripherally attached to the plasma membrane. From initiation until emergence from the primary root, lateral root primordia are surrounded by several layers of differentiated tissues with a complex cell wall composition that interferes with the efficient penetration of all buffers. Therefore, immunolocalization in early lateral root primordia requires a modified method, including a strong solvent treatment for removal of hydrophobic barriers and a specific cocktail of cell wall-degrading enzymes. The presented method allows for easy, reliable, and high-quality in situ detection of the subcellular localization of endogenous proteins in primary and lateral root meristems without the need of time-consuming crosses or making translational fusions to fluorescent proteins. alternative_title: - Methods in Molecular Biology author: - first_name: Michael full_name: Karampelias, Michael last_name: Karampelias - first_name: Ricardo full_name: Tejos, Ricardo last_name: Tejos - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Steffen full_name: Vanneste, Steffen last_name: Vanneste citation: ama: 'Karampelias M, Tejos R, Friml J, Vanneste S. Optimized whole mount in situ immunolocalization for Arabidopsis thaliana  root meristems and lateral root primordia. In: Ristova D, Barbez E, eds. Root Development. Methods and Protocols. Vol 1761. MIMB. Springer; 2018:131-143. doi:10.1007/978-1-4939-7747-5_10' apa: Karampelias, M., Tejos, R., Friml, J., & Vanneste, S. (2018). Optimized whole mount in situ immunolocalization for Arabidopsis thaliana  root meristems and lateral root primordia. In D. Ristova & E. Barbez (Eds.), Root Development. Methods and Protocols (Vol. 1761, pp. 131–143). Springer. https://doi.org/10.1007/978-1-4939-7747-5_10 chicago: Karampelias, Michael, Ricardo Tejos, Jiří Friml, and Steffen Vanneste. “Optimized Whole Mount in Situ Immunolocalization for Arabidopsis Thaliana  Root Meristems and Lateral Root Primordia.” In Root Development. Methods and Protocols, edited by Daniela Ristova and Elke Barbez, 1761:131–43. MIMB. Springer, 2018. https://doi.org/10.1007/978-1-4939-7747-5_10. ieee: M. Karampelias, R. Tejos, J. Friml, and S. Vanneste, “Optimized whole mount in situ immunolocalization for Arabidopsis thaliana  root meristems and lateral root primordia,” in Root Development. Methods and Protocols, vol. 1761, D. Ristova and E. Barbez, Eds. Springer, 2018, pp. 131–143. ista: 'Karampelias M, Tejos R, Friml J, Vanneste S. 2018.Optimized whole mount in situ immunolocalization for Arabidopsis thaliana  root meristems and lateral root primordia. In: Root Development. Methods and Protocols. Methods in Molecular Biology, vol. 1761, 131–143.' mla: Karampelias, Michael, et al. “Optimized Whole Mount in Situ Immunolocalization for Arabidopsis Thaliana  Root Meristems and Lateral Root Primordia.” Root Development. Methods and Protocols, edited by Daniela Ristova and Elke Barbez, vol. 1761, Springer, 2018, pp. 131–43, doi:10.1007/978-1-4939-7747-5_10. short: M. Karampelias, R. Tejos, J. Friml, S. Vanneste, in:, D. Ristova, E. Barbez (Eds.), Root Development. Methods and Protocols, Springer, 2018, pp. 131–143. date_created: 2018-12-11T11:46:20Z date_published: 2018-03-11T00:00:00Z date_updated: 2021-01-12T07:54:34Z day: '11' department: - _id: JiFr doi: 10.1007/978-1-4939-7747-5_10 editor: - first_name: Daniela full_name: Ristova, Daniela last_name: Ristova - first_name: Elke full_name: Barbez, Elke last_name: Barbez intvolume: ' 1761' language: - iso: eng month: '03' oa_version: None page: 131 - 143 publication: Root Development. Methods and Protocols publication_status: published publisher: Springer publist_id: '7418' quality_controlled: '1' scopus_import: 1 series_title: MIMB status: public title: Optimized whole mount in situ immunolocalization for Arabidopsis thaliana root meristems and lateral root primordia type: book_chapter user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87 volume: 1761 year: '2018' ... --- _id: '203' abstract: - lang: eng text: Asymmetric auxin distribution is instrumental for the differential growth that causes organ bending on tropic stimuli and curvatures during plant development. Local differences in auxin concentrations are achieved mainly by polarized cellular distribution of PIN auxin transporters, but whether other mechanisms involving auxin homeostasis are also relevant for the formation of auxin gradients is not clear. Here we show that auxin methylation is required for asymmetric auxin distribution across the hypocotyl, particularly during its response to gravity. We found that loss-of-function mutants in Arabidopsis IAA CARBOXYL METHYLTRANSFERASE1 (IAMT1) prematurely unfold the apical hook, and that their hypocotyls are impaired in gravitropic reorientation. This defect is linked to an auxin-dependent increase in PIN gene expression, leading to an increased polar auxin transport and lack of asymmetric distribution of PIN3 in the iamt1 mutant. Gravitropic reorientation in the iamt1 mutant could be restored with either endodermis-specific expression of IAMT1 or partial inhibition of polar auxin transport, which also results in normal PIN gene expression levels. We propose that IAA methylation is necessary in gravity-sensing cells to restrict polar auxin transport within the range of auxin levels that allow for differential responses. article_processing_charge: No author: - first_name: Mohamad full_name: Abbas, Mohamad id: 47E8FC1C-F248-11E8-B48F-1D18A9856A87 last_name: Abbas - first_name: García J full_name: Hernández, García J last_name: Hernández - first_name: Stephan full_name: Pollmann, Stephan last_name: Pollmann - first_name: Sophia L full_name: Samodelov, Sophia L last_name: Samodelov - first_name: Martina full_name: Kolb, Martina last_name: Kolb - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Ulrich Z full_name: Hammes, Ulrich Z last_name: Hammes - first_name: Matias D full_name: Zurbriggen, Matias D last_name: Zurbriggen - first_name: Miguel full_name: Blázquez, Miguel last_name: Blázquez - first_name: David full_name: Alabadí, David last_name: Alabadí citation: ama: Abbas M, Hernández GJ, Pollmann S, et al. Auxin methylation is required for differential growth in Arabidopsis. PNAS. 2018;115(26):6864-6869. doi:10.1073/pnas.1806565115 apa: Abbas, M., Hernández, G. J., Pollmann, S., Samodelov, S. L., Kolb, M., Friml, J., … Alabadí, D. (2018). Auxin methylation is required for differential growth in Arabidopsis. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1806565115 chicago: Abbas, Mohamad, García J Hernández, Stephan Pollmann, Sophia L Samodelov, Martina Kolb, Jiří Friml, Ulrich Z Hammes, Matias D Zurbriggen, Miguel Blázquez, and David Alabadí. “Auxin Methylation Is Required for Differential Growth in Arabidopsis.” PNAS. National Academy of Sciences, 2018. https://doi.org/10.1073/pnas.1806565115. ieee: M. Abbas et al., “Auxin methylation is required for differential growth in Arabidopsis,” PNAS, vol. 115, no. 26. National Academy of Sciences, pp. 6864–6869, 2018. ista: Abbas M, Hernández GJ, Pollmann S, Samodelov SL, Kolb M, Friml J, Hammes UZ, Zurbriggen MD, Blázquez M, Alabadí D. 2018. Auxin methylation is required for differential growth in Arabidopsis. PNAS. 115(26), 6864–6869. mla: Abbas, Mohamad, et al. “Auxin Methylation Is Required for Differential Growth in Arabidopsis.” PNAS, vol. 115, no. 26, National Academy of Sciences, 2018, pp. 6864–69, doi:10.1073/pnas.1806565115. short: M. Abbas, G.J. Hernández, S. Pollmann, S.L. Samodelov, M. Kolb, J. Friml, U.Z. Hammes, M.D. Zurbriggen, M. Blázquez, D. Alabadí, PNAS 115 (2018) 6864–6869. date_created: 2018-12-11T11:45:11Z date_published: 2018-06-26T00:00:00Z date_updated: 2023-09-08T13:24:40Z day: '26' department: - _id: JiFr doi: 10.1073/pnas.1806565115 ec_funded: 1 external_id: isi: - '000436245000096' intvolume: ' 115' isi: 1 issue: '26' language: - iso: eng main_file_link: - open_access: '1' url: http://eprints.nottingham.ac.uk/52388/ month: '06' oa: 1 oa_version: None page: 6864-6869 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: PNAS publication_status: published publisher: National Academy of Sciences publist_id: '7710' quality_controlled: '1' scopus_import: '1' status: public title: Auxin methylation is required for differential growth in Arabidopsis type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 115 year: '2018' ... --- _id: '5830' abstract: - lang: eng text: CLE peptides have been implicated in various developmental processes of plants and mediate their responses to environmental stimuli. However, the biological relevance of most CLE genes remains to be functionally characterized. Here, we report that CLE9, which is expressed in stomata, acts as an essential regulator in the induction of stomatal closure. Exogenous application of CLE9 peptides or overexpression of CLE9 effectively led to stomatal closure and enhanced drought tolerance, whereas CLE9 loss-of-function mutants were sensitivity to drought stress. CLE9-induced stomatal closure was impaired in abscisic acid (ABA)-deficient mutants, indicating that ABA is required for CLE9-medaited guard cell signalling. We further deciphered that two guard cell ABA-signalling components, OST1 and SLAC1, were responsible for CLE9-induced stomatal closure. MPK3 and MPK6 were activated by the CLE9 peptide, and CLE9 peptides failed to close stomata in mpk3 and mpk6 mutants. In addition, CLE9 peptides stimulated the induction of hydrogen peroxide (H2O2) and nitric oxide (NO) synthesis associated with stomatal closure, which was abolished in the NADPH oxidase-deficient mutants or nitric reductase mutants, respectively. Collectively, our results reveal a novel ABA-dependent function of CLE9 in the regulation of stomatal apertures, thereby suggesting a potential role of CLE9 in the stress acclimatization of plants. article_processing_charge: No author: - first_name: Luosha full_name: Zhang, Luosha last_name: Zhang - first_name: Xiong full_name: Shi, Xiong last_name: Shi - first_name: Yutao full_name: Zhang, Yutao last_name: Zhang - first_name: Jiajing full_name: Wang, Jiajing last_name: Wang - first_name: Jingwei full_name: Yang, Jingwei last_name: Yang - first_name: Takashi full_name: Ishida, Takashi last_name: Ishida - first_name: Wenqian full_name: Jiang, Wenqian last_name: Jiang - first_name: Xiangyu full_name: Han, Xiangyu last_name: Han - first_name: Jingke full_name: Kang, Jingke last_name: Kang - first_name: Xuening full_name: Wang, Xuening last_name: Wang - first_name: Lixia full_name: Pan, Lixia last_name: Pan - first_name: Shuo full_name: Lv, Shuo last_name: Lv - first_name: Bing full_name: Cao, Bing last_name: Cao - first_name: Yonghong full_name: Zhang, Yonghong last_name: Zhang - first_name: Jinbin full_name: Wu, Jinbin last_name: Wu - first_name: Huibin full_name: Han, Huibin id: 31435098-F248-11E8-B48F-1D18A9856A87 last_name: Han - first_name: Zhubing full_name: Hu, Zhubing last_name: Hu - first_name: Langjun full_name: Cui, Langjun last_name: Cui - first_name: Shinichiro full_name: Sawa, Shinichiro last_name: Sawa - first_name: Junmin full_name: He, Junmin last_name: He - first_name: Guodong full_name: Wang, Guodong last_name: Wang citation: ama: Zhang L, Shi X, Zhang Y, et al. CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana. Plant Cell and Environment. 2018. doi:10.1111/pce.13475 apa: Zhang, L., Shi, X., Zhang, Y., Wang, J., Yang, J., Ishida, T., … Wang, G. (2018). CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana. Plant Cell and Environment. Wiley. https://doi.org/10.1111/pce.13475 chicago: Zhang, Luosha, Xiong Shi, Yutao Zhang, Jiajing Wang, Jingwei Yang, Takashi Ishida, Wenqian Jiang, et al. “CLE9 Peptide-Induced Stomatal Closure Is Mediated by Abscisic Acid, Hydrogen Peroxide, and Nitric Oxide in Arabidopsis Thaliana.” Plant Cell and Environment. Wiley, 2018. https://doi.org/10.1111/pce.13475. ieee: L. Zhang et al., “CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana,” Plant Cell and Environment. Wiley, 2018. ista: Zhang L, Shi X, Zhang Y, Wang J, Yang J, Ishida T, Jiang W, Han X, Kang J, Wang X, Pan L, Lv S, Cao B, Zhang Y, Wu J, Han H, Hu Z, Cui L, Sawa S, He J, Wang G. 2018. CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana. Plant Cell and Environment. mla: Zhang, Luosha, et al. “CLE9 Peptide-Induced Stomatal Closure Is Mediated by Abscisic Acid, Hydrogen Peroxide, and Nitric Oxide in Arabidopsis Thaliana.” Plant Cell and Environment, Wiley, 2018, doi:10.1111/pce.13475. short: L. Zhang, X. Shi, Y. Zhang, J. Wang, J. Yang, T. Ishida, W. Jiang, X. Han, J. Kang, X. Wang, L. Pan, S. Lv, B. Cao, Y. Zhang, J. Wu, H. Han, Z. Hu, L. Cui, S. Sawa, J. He, G. Wang, Plant Cell and Environment (2018). date_created: 2019-01-13T22:59:11Z date_published: 2018-10-31T00:00:00Z date_updated: 2023-09-11T12:43:31Z day: '31' department: - _id: JiFr doi: 10.1111/pce.13475 external_id: isi: - '000459014800021' pmid: - '30378140' isi: 1 language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pubmed/30378140 month: '10' oa: 1 oa_version: Published Version pmid: 1 publication: Plant Cell and Environment publication_identifier: issn: - '01407791' publication_status: epub_ahead publisher: Wiley quality_controlled: '1' scopus_import: '1' status: public title: CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 year: '2018' ... --- _id: '428' abstract: - lang: eng text: The plant hormone gibberellic acid (GA) is a crucial regulator of growth and development. The main paradigm of GA signaling puts forward transcriptional regulation via the degradation of DELLA transcriptional repressors. GA has also been shown to regulate tropic responses by modulation of the plasma membrane incidence of PIN auxin transporters by an unclear mechanism. Here we uncovered the cellular and molecular mechanisms by which GA redirects protein trafficking and thus regulates cell surface functionality. Photoconvertible reporters revealed that GA balances the protein traffic between the vacuole degradation route and recycling back to the cell surface. Low GA levels promote vacuolar delivery and degradation of multiple cargos, including PIN proteins, whereas high GA levels promote their recycling to the plasma membrane. This GA effect requires components of the retromer complex, such as Sorting Nexin 1 (SNX1) and its interacting, microtubule (MT)-associated protein, the Cytoplasmic Linker-Associated Protein (CLASP1). Accordingly, GA regulates the subcellular distribution of SNX1 and CLASP1, and the intact MT cytoskeleton is essential for the GA effect on trafficking. This GA cellular action occurs through DELLA proteins that regulate the MT and retromer presumably via their interaction partners Prefoldins (PFDs). Our study identified a branching of the GA signaling pathway at the level of DELLA proteins, which, in parallel to regulating transcription, also target by a nontranscriptional mechanism the retromer complex acting at the intersection of the degradation and recycling trafficking routes. By this mechanism, GA can redirect receptors and transporters to the cell surface, thus coregulating multiple processes, including PIN-dependent auxin fluxes during tropic responses. acknowledgement: "We gratefully acknowledge M. Blázquez (Instituto de Biología Molecular y Celular de Plantas), M. Fendrych, C. Cuesta Moliner (Institute of Science and Technology Austria), M. Vanstraelen, M. Nowack (Center for Plant Systems Biology, Ghent), C. Luschnig (Universitat fur Bodenkultur Wien, Vienna), S. Simon (Central European Institute of Technology, Brno), C. Sommerville (Carnegie Institution for Science), and Y. Gu (Penn State University) for making available the materials used in this study;\r\n...funding from the European Research Council (ERC) under the European Union’s Seventh Framework Programme (FP7/2007-2013)/ERC Grant Agreement 282300.\r\nCC BY NC ND" article_processing_charge: No author: - first_name: Yuliya full_name: Salanenka, Yuliya id: 46DAAE7E-F248-11E8-B48F-1D18A9856A87 last_name: Salanenka - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Christian full_name: Löfke, Christian last_name: Löfke - first_name: Kaori full_name: Tabata, Kaori id: 7DAAEDA4-02D0-11E9-B11A-A5A4D7DFFFD0 last_name: Tabata - first_name: Satoshi full_name: Naramoto, Satoshi last_name: Naramoto - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Salanenka Y, Verstraeten I, Löfke C, et al. Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane. PNAS. 2018;115(14):3716-3721. doi:10.1073/pnas.1721760115 apa: Salanenka, Y., Verstraeten, I., Löfke, C., Tabata, K., Naramoto, S., Glanc, M., & Friml, J. (2018). Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1721760115 chicago: Salanenka, Yuliya, Inge Verstraeten, Christian Löfke, Kaori Tabata, Satoshi Naramoto, Matous Glanc, and Jiří Friml. “Gibberellin DELLA Signaling Targets the Retromer Complex to Redirect Protein Trafficking to the Plasma Membrane.” PNAS. National Academy of Sciences, 2018. https://doi.org/10.1073/pnas.1721760115. ieee: Y. Salanenka et al., “Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane,” PNAS, vol. 115, no. 14. National Academy of Sciences, pp. 3716–3721, 2018. ista: Salanenka Y, Verstraeten I, Löfke C, Tabata K, Naramoto S, Glanc M, Friml J. 2018. Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane. PNAS. 115(14), 3716–3721. mla: Salanenka, Yuliya, et al. “Gibberellin DELLA Signaling Targets the Retromer Complex to Redirect Protein Trafficking to the Plasma Membrane.” PNAS, vol. 115, no. 14, National Academy of Sciences, 2018, pp. 3716–21, doi:10.1073/pnas.1721760115. short: Y. Salanenka, I. Verstraeten, C. Löfke, K. Tabata, S. Naramoto, M. Glanc, J. Friml, PNAS 115 (2018) 3716–3721. date_created: 2018-12-11T11:46:25Z date_published: 2018-04-03T00:00:00Z date_updated: 2023-09-11T14:06:34Z day: '03' ddc: - '580' department: - _id: JiFr doi: 10.1073/pnas.1721760115 ec_funded: 1 external_id: isi: - '000429012500073' file: - access_level: open_access checksum: 1fcf7223fb8f99559cfa80bd6f24ce44 content_type: application/pdf creator: dernst date_created: 2018-12-17T12:30:14Z date_updated: 2020-07-14T12:46:26Z file_id: '5700' file_name: 2018_PNAS_Salanenka.pdf file_size: 1924101 relation: main_file file_date_updated: 2020-07-14T12:46:26Z has_accepted_license: '1' intvolume: ' 115' isi: 1 issue: '14' language: - iso: eng month: '04' oa: 1 oa_version: Published Version page: ' 3716 - 3721' project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: PNAS publication_status: published publisher: National Academy of Sciences publist_id: '7395' quality_controlled: '1' scopus_import: '1' status: public title: Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 115 year: '2018' ... --- _id: '280' abstract: - lang: eng text: Flowers have a species-specific functional life span that determines the time window in which pollination, fertilization and seed set can occur. The stigma tissue plays a key role in flower receptivity by intercepting pollen and initiating pollen tube growth toward the ovary. In this article, we show that a developmentally controlled cell death programme terminates the functional life span of stigma cells in Arabidopsis. We identified the leaf senescence regulator ORESARA1 (also known as ANAC092) and the previously uncharacterized KIRA1 (also known as ANAC074) as partially redundant transcription factors that modulate stigma longevity by controlling the expression of programmed cell death-associated genes. KIRA1 expression is sufficient to induce cell death and terminate floral receptivity, whereas lack of both KIRA1 and ORESARA1 substantially increases stigma life span. Surprisingly, the extension of stigma longevity is accompanied by only a moderate extension of flower receptivity, suggesting that additional processes participate in the control of the flower's receptive life span. acknowledgement: We gratefully acknowledge funding from the Chinese Scholarship Council (CSC; project number 201206910025 to Z.G.), the Fonds Wetenschappelijk Onderzoek (FWO; project number G005112N to A.D.; fellowship number 12I7417N to Z.L.), the Belgian Federal Science Policy Office (BELSPO; to Y.S.), the Agency for Innovation by Science and Technology of Belgium (IWT; fellowship number 121110 to M.V.D.), the Hercules foundation (grant AUGE-09-029 to K.D.), and the ERC StG PROCELLDEATH (project number 639234 to M.K.N.). article_processing_charge: No author: - first_name: Zhen full_name: Gao, Zhen last_name: Gao - first_name: Anna full_name: Daneva, Anna last_name: Daneva - first_name: Yuliya full_name: Salanenka, Yuliya id: 46DAAE7E-F248-11E8-B48F-1D18A9856A87 last_name: Salanenka - first_name: Matthias full_name: Van Durme, Matthias last_name: Van Durme - first_name: Marlies full_name: Huysmans, Marlies last_name: Huysmans - first_name: Zongcheng full_name: Lin, Zongcheng last_name: Lin - first_name: Freya full_name: De Winter, Freya last_name: De Winter - first_name: Steffen full_name: Vanneste, Steffen last_name: Vanneste - first_name: Mansour full_name: Karimi, Mansour last_name: Karimi - first_name: Jan full_name: Van De Velde, Jan last_name: Van De Velde - first_name: Klaas full_name: Vandepoele, Klaas last_name: Vandepoele - first_name: Davy full_name: Van De Walle, Davy last_name: Van De Walle - first_name: Koen full_name: Dewettinck, Koen last_name: Dewettinck - first_name: Bart full_name: Lambrecht, Bart last_name: Lambrecht - first_name: Moritz full_name: Nowack, Moritz last_name: Nowack citation: ama: Gao Z, Daneva A, Salanenka Y, et al. KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in the stigma of Arabidopsis. Nature Plants. 2018;4(6):365-375. doi:10.1038/s41477-018-0160-7 apa: Gao, Z., Daneva, A., Salanenka, Y., Van Durme, M., Huysmans, M., Lin, Z., … Nowack, M. (2018). KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in the stigma of Arabidopsis. Nature Plants. Nature Publishing Group. https://doi.org/10.1038/s41477-018-0160-7 chicago: Gao, Zhen, Anna Daneva, Yuliya Salanenka, Matthias Van Durme, Marlies Huysmans, Zongcheng Lin, Freya De Winter, et al. “KIRA1 and ORESARA1 Terminate Flower Receptivity by Promoting Cell Death in the Stigma of Arabidopsis.” Nature Plants. Nature Publishing Group, 2018. https://doi.org/10.1038/s41477-018-0160-7. ieee: Z. Gao et al., “KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in the stigma of Arabidopsis,” Nature Plants, vol. 4, no. 6. Nature Publishing Group, pp. 365–375, 2018. ista: Gao Z, Daneva A, Salanenka Y, Van Durme M, Huysmans M, Lin Z, De Winter F, Vanneste S, Karimi M, Van De Velde J, Vandepoele K, Van De Walle D, Dewettinck K, Lambrecht B, Nowack M. 2018. KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in the stigma of Arabidopsis. Nature Plants. 4(6), 365–375. mla: Gao, Zhen, et al. “KIRA1 and ORESARA1 Terminate Flower Receptivity by Promoting Cell Death in the Stigma of Arabidopsis.” Nature Plants, vol. 4, no. 6, Nature Publishing Group, 2018, pp. 365–75, doi:10.1038/s41477-018-0160-7. short: Z. Gao, A. Daneva, Y. Salanenka, M. Van Durme, M. Huysmans, Z. Lin, F. De Winter, S. Vanneste, M. Karimi, J. Van De Velde, K. Vandepoele, D. Van De Walle, K. Dewettinck, B. Lambrecht, M. Nowack, Nature Plants 4 (2018) 365–375. date_created: 2018-12-11T11:45:35Z date_published: 2018-05-28T00:00:00Z date_updated: 2023-09-13T08:24:17Z day: '28' department: - _id: JiFr doi: 10.1038/s41477-018-0160-7 external_id: isi: - '000435571000017' intvolume: ' 4' isi: 1 issue: '6' language: - iso: eng month: '05' oa_version: None page: 365 - 375 publication: Nature Plants publication_status: published publisher: Nature Publishing Group publist_id: '7619' quality_controlled: '1' scopus_import: '1' status: public title: KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in the stigma of Arabidopsis type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 4 year: '2018' ... --- _id: '158' abstract: - lang: eng text: 'The angiosperm seed is composed of three genetically distinct tissues: the diploid embryo that originates from the fertilized egg cell, the triploid endosperm that is produced from the fertilized central cell, and the maternal sporophytic integuments that develop into the seed coat1. At the onset of embryo development in Arabidopsis thaliana, the zygote divides asymmetrically, producing a small apical embryonic cell and a larger basal cell that connects the embryo to the maternal tissue2. The coordinated and synchronous development of the embryo and the surrounding integuments, and the alignment of their growth axes, suggest communication between maternal tissues and the embryo. In contrast to animals, however, where a network of maternal factors that direct embryo patterning have been identified3,4, only a few maternal mutations have been described to affect embryo development in plants5–7. Early embryo patterning in Arabidopsis requires accumulation of the phytohormone auxin in the apical cell by directed transport from the suspensor8–10. However, the origin of this auxin has remained obscure. Here we investigate the source of auxin for early embryogenesis and provide evidence that the mother plant coordinates seed development by supplying auxin to the early embryo from the integuments of the ovule. We show that auxin response increases in ovules after fertilization, due to upregulated auxin biosynthesis in the integuments, and this maternally produced auxin is required for correct embryo development.' acknowledgement: This work was further supported by the Czech Science Foundation GACR (GA13-40637S) to J.F.; article_processing_charge: No author: - first_name: Hélène full_name: Robert, Hélène last_name: Robert - first_name: Chulmin full_name: Park, Chulmin last_name: Park - first_name: Carla full_name: Gutièrrez, Carla last_name: Gutièrrez - first_name: Barbara full_name: Wójcikowska, Barbara last_name: Wójcikowska - first_name: Aleš full_name: Pěnčík, Aleš last_name: Pěnčík - first_name: Ondřej full_name: Novák, Ondřej last_name: Novák - first_name: Junyi full_name: Chen, Junyi last_name: Chen - first_name: Wim full_name: Grunewald, Wim last_name: Grunewald - first_name: Thomas full_name: Dresselhaus, Thomas last_name: Dresselhaus - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Thomas full_name: Laux, Thomas last_name: Laux citation: ama: Robert H, Park C, Gutièrrez C, et al. Maternal auxin supply contributes to early embryo patterning in Arabidopsis. Nature Plants. 2018;4(8):548-553. doi:10.1038/s41477-018-0204-z apa: Robert, H., Park, C., Gutièrrez, C., Wójcikowska, B., Pěnčík, A., Novák, O., … Laux, T. (2018). Maternal auxin supply contributes to early embryo patterning in Arabidopsis. Nature Plants. Nature Publishing Group. https://doi.org/10.1038/s41477-018-0204-z chicago: Robert, Hélène, Chulmin Park, Carla Gutièrrez, Barbara Wójcikowska, Aleš Pěnčík, Ondřej Novák, Junyi Chen, et al. “Maternal Auxin Supply Contributes to Early Embryo Patterning in Arabidopsis.” Nature Plants. Nature Publishing Group, 2018. https://doi.org/10.1038/s41477-018-0204-z. ieee: H. Robert et al., “Maternal auxin supply contributes to early embryo patterning in Arabidopsis,” Nature Plants, vol. 4, no. 8. Nature Publishing Group, pp. 548–553, 2018. ista: Robert H, Park C, Gutièrrez C, Wójcikowska B, Pěnčík A, Novák O, Chen J, Grunewald W, Dresselhaus T, Friml J, Laux T. 2018. Maternal auxin supply contributes to early embryo patterning in Arabidopsis. Nature Plants. 4(8), 548–553. mla: Robert, Hélène, et al. “Maternal Auxin Supply Contributes to Early Embryo Patterning in Arabidopsis.” Nature Plants, vol. 4, no. 8, Nature Publishing Group, 2018, pp. 548–53, doi:10.1038/s41477-018-0204-z. short: H. Robert, C. Park, C. Gutièrrez, B. Wójcikowska, A. Pěnčík, O. Novák, J. Chen, W. Grunewald, T. Dresselhaus, J. Friml, T. Laux, Nature Plants 4 (2018) 548–553. date_created: 2018-12-11T11:44:56Z date_published: 2018-07-16T00:00:00Z date_updated: 2023-09-13T08:53:28Z day: '16' department: - _id: JiFr doi: 10.1038/s41477-018-0204-z ec_funded: 1 external_id: isi: - '000443861300011' pmid: - '30013211' intvolume: ' 4' isi: 1 issue: '8' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pubmed/30013211 month: '07' oa: 1 oa_version: Submitted Version page: 548 - 553 pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: Nature Plants publication_status: published publisher: Nature Publishing Group publist_id: '7763' quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/plant-mothers-talk-to-their-embryos-via-the-hormone-auxin/ scopus_import: '1' status: public title: Maternal auxin supply contributes to early embryo patterning in Arabidopsis type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 4 year: '2018' ... --- _id: '462' abstract: - lang: eng text: 'AtNHX5 and AtNHX6 are endosomal Na+,K+/H+ antiporters that are critical for growth and development in Arabidopsis, but the mechanism behind their action remains unknown. Here, we report that AtNHX5 and AtNHX6, functioning as H+ leak, control auxin homeostasis and auxin-mediated development. We found that nhx5 nhx6 exhibited growth variations of auxin-related defects. We further showed that nhx5 nhx6 was affected in auxin homeostasis. Genetic analysis showed that AtNHX5 and AtNHX6 were required for the function of the ER-localized auxin transporter PIN5. Although AtNHX5 and AtNHX6 were co-localized with PIN5 at ER, they did not interact directly. Instead, the conserved acidic residues in AtNHX5 and AtNHX6, which are essential for exchange activity, were required for PIN5 function. AtNHX5 and AtNHX6 regulated the pH in ER. Overall, AtNHX5 and AtNHX6 may regulate auxin transport across the ER via the pH gradient created by their transport activity. H+-leak pathway provides a fine-tuning mechanism that controls cellular auxin fluxes. ' acknowledgement: 'This work was supported by the National Natural Science Foundation of China (31571464, 31371438 and 31070222 to Q.S.Q.), the National Basic Research Program of China (973 project, 2013CB429904 to Q.S.Q.), the Research Fund for the Doctoral Program of Higher Education of China (20130211110001 to Q.S.Q.), the Ministry of Education, Youth and Sports of the Czech Republic (the National Program for Sustainability I, LO1204), and The Czech Science Foundation GAČR (GA13–40637S) to JF. We thank Dr. Tom J. Guilfoyle for DR5::GUS line and Dr. Jia Li for pBIB‐RFP vector and DR5::GFP line. We thank Liping Guan and Yang Zhao for their help with the confocal microscope assay. ' article_processing_charge: No article_type: original author: - first_name: Ligang full_name: Fan, Ligang last_name: Fan - first_name: Lei full_name: Zhao, Lei last_name: Zhao - first_name: Wei full_name: Hu, Wei last_name: Hu - first_name: Weina full_name: Li, Weina last_name: Li - first_name: Ondřej full_name: Novák, Ondřej last_name: Novák - first_name: Miroslav full_name: Strnad, Miroslav last_name: Strnad - first_name: Sibu full_name: Simon, Sibu id: 4542EF9A-F248-11E8-B48F-1D18A9856A87 last_name: Simon orcid: 0000-0002-1998-6741 - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Jinbo full_name: Shen, Jinbo last_name: Shen - first_name: Liwen full_name: Jiang, Liwen last_name: Jiang - first_name: Quan full_name: Qiu, Quan last_name: Qiu citation: ama: Fan L, Zhao L, Hu W, et al. NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development. Plant, Cell and Environment. 2018;41:850-864. doi:10.1111/pce.13153 apa: Fan, L., Zhao, L., Hu, W., Li, W., Novák, O., Strnad, M., … Qiu, Q. (2018). NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development. Plant, Cell and Environment. Wiley-Blackwell. https://doi.org/10.1111/pce.13153 chicago: Fan, Ligang, Lei Zhao, Wei Hu, Weina Li, Ondřej Novák, Miroslav Strnad, Sibu Simon, et al. “NHX Antiporters Regulate the PH of Endoplasmic Reticulum and Auxin-Mediated Development.” Plant, Cell and Environment. Wiley-Blackwell, 2018. https://doi.org/10.1111/pce.13153. ieee: L. Fan et al., “NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development,” Plant, Cell and Environment, vol. 41. Wiley-Blackwell, pp. 850–864, 2018. ista: Fan L, Zhao L, Hu W, Li W, Novák O, Strnad M, Simon S, Friml J, Shen J, Jiang L, Qiu Q. 2018. NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development. Plant, Cell and Environment. 41, 850–864. mla: Fan, Ligang, et al. “NHX Antiporters Regulate the PH of Endoplasmic Reticulum and Auxin-Mediated Development.” Plant, Cell and Environment, vol. 41, Wiley-Blackwell, 2018, pp. 850–64, doi:10.1111/pce.13153. short: L. Fan, L. Zhao, W. Hu, W. Li, O. Novák, M. Strnad, S. Simon, J. Friml, J. Shen, L. Jiang, Q. Qiu, Plant, Cell and Environment 41 (2018) 850–864. date_created: 2018-12-11T11:46:36Z date_published: 2018-05-01T00:00:00Z date_updated: 2023-09-13T09:03:18Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1111/pce.13153 external_id: isi: - '000426870500012' pmid: - '29360148' file: - access_level: open_access checksum: 6a20f843565f962cb20281cdf5e40914 content_type: application/pdf creator: dernst date_created: 2019-11-18T16:22:22Z date_updated: 2020-07-14T12:46:32Z file_id: '7042' file_name: 2018_PlantCellEnv_Fan.pdf file_size: 1937976 relation: main_file file_date_updated: 2020-07-14T12:46:32Z has_accepted_license: '1' intvolume: ' 41' isi: 1 language: - iso: eng month: '05' oa: 1 oa_version: Submitted Version page: 850 - 864 pmid: 1 publication: Plant, Cell and Environment publication_status: published publisher: Wiley-Blackwell publist_id: '7359' quality_controlled: '1' scopus_import: '1' status: public title: NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development tmp: image: /images/cc_by_nc.png legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) short: CC BY-NC (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 41 year: '2018' ... --- _id: '192' abstract: - lang: eng text: The phytohormone auxin is the information carrier in a plethora of developmental and physiological processes in plants(1). It has been firmly established that canonical, nuclear auxin signalling acts through regulation of gene transcription(2). Here, we combined microfluidics, live imaging, genetic engineering and computational modelling to reanalyse the classical case of root growth inhibition(3) by auxin. We show that Arabidopsis roots react to addition and removal of auxin by extremely rapid adaptation of growth rate. This process requires intracellular auxin perception but not transcriptional reprogramming. The formation of the canonical TIR1/AFB-Aux/IAA co-receptor complex is required for the growth regulation, hinting to a novel, non-transcriptional branch of this signalling pathway. Our results challenge the current understanding of root growth regulation by auxin and suggest another, presumably non-transcriptional, signalling output of the canonical auxin pathway. article_processing_charge: No article_type: original author: - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Maria full_name: Akhmanova, Maria id: 3425EC26-F248-11E8-B48F-1D18A9856A87 last_name: Akhmanova orcid: 0000-0003-1522-3162 - first_name: Jack full_name: Merrin, Jack id: 4515C308-F248-11E8-B48F-1D18A9856A87 last_name: Merrin orcid: 0000-0001-5145-4609 - first_name: Matous full_name: Glanc, Matous last_name: Glanc - first_name: Shinya full_name: Hagihara, Shinya last_name: Hagihara - first_name: Koji full_name: Takahashi, Koji last_name: Takahashi - first_name: Naoyuki full_name: Uchida, Naoyuki last_name: Uchida - first_name: Keiko U full_name: Torii, Keiko U last_name: Torii - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Fendrych M, Akhmanova M, Merrin J, et al. Rapid and reversible root growth inhibition by TIR1 auxin signalling. Nature Plants. 2018;4(7):453-459. doi:10.1038/s41477-018-0190-1 apa: Fendrych, M., Akhmanova, M., Merrin, J., Glanc, M., Hagihara, S., Takahashi, K., … Friml, J. (2018). Rapid and reversible root growth inhibition by TIR1 auxin signalling. Nature Plants. Springer Nature. https://doi.org/10.1038/s41477-018-0190-1 chicago: Fendrych, Matyas, Maria Akhmanova, Jack Merrin, Matous Glanc, Shinya Hagihara, Koji Takahashi, Naoyuki Uchida, Keiko U Torii, and Jiří Friml. “Rapid and Reversible Root Growth Inhibition by TIR1 Auxin Signalling.” Nature Plants. Springer Nature, 2018. https://doi.org/10.1038/s41477-018-0190-1. ieee: M. Fendrych et al., “Rapid and reversible root growth inhibition by TIR1 auxin signalling,” Nature Plants, vol. 4, no. 7. Springer Nature, pp. 453–459, 2018. ista: Fendrych M, Akhmanova M, Merrin J, Glanc M, Hagihara S, Takahashi K, Uchida N, Torii KU, Friml J. 2018. Rapid and reversible root growth inhibition by TIR1 auxin signalling. Nature Plants. 4(7), 453–459. mla: Fendrych, Matyas, et al. “Rapid and Reversible Root Growth Inhibition by TIR1 Auxin Signalling.” Nature Plants, vol. 4, no. 7, Springer Nature, 2018, pp. 453–59, doi:10.1038/s41477-018-0190-1. short: M. Fendrych, M. Akhmanova, J. Merrin, M. Glanc, S. Hagihara, K. Takahashi, N. Uchida, K.U. Torii, J. Friml, Nature Plants 4 (2018) 453–459. date_created: 2018-12-11T11:45:07Z date_published: 2018-06-25T00:00:00Z date_updated: 2023-09-15T12:11:03Z day: '25' department: - _id: JiFr - _id: DaSi - _id: NanoFab doi: 10.1038/s41477-018-0190-1 external_id: isi: - '000443221200017' pmid: - '29942048' intvolume: ' 4' isi: 1 issue: '7' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pubmed/29942048 month: '06' oa: 1 oa_version: Submitted Version page: 453 - 459 pmid: 1 publication: Nature Plants publication_status: published publisher: Springer Nature publist_id: '7728' quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/new-mechanism-for-the-plant-hormone-auxin-discovered/ scopus_import: '1' status: public title: Rapid and reversible root growth inhibition by TIR1 auxin signalling type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 4 year: '2018' ... --- _id: '14' abstract: - lang: eng text: The intercellular transport of auxin is driven by PIN-formed (PIN) auxin efflux carriers. PINs are localized at the plasma membrane (PM) and on constitutively recycling endomembrane vesicles. Therefore, PINs can mediate auxin transport either by direct translocation across the PM or by pumping auxin into secretory vesicles (SVs), leading to its secretory release upon fusion with the PM. Which of these two mechanisms dominates is a matter of debate. Here, we addressed the issue with a mathematical modeling approach. We demonstrate that the efficiency of secretory transport depends on SV size, half-life of PINs on the PM, pH, exocytosis frequency and PIN density. 3D structured illumination microscopy (SIM) was used to determine PIN density on the PM. Combining this data with published values of the other parameters, we show that the transport activity of PINs in SVs would have to be at least 1000× greater than on the PM in order to produce a comparable macroscopic auxin transport. If both transport mechanisms operated simultaneously and PINs were equally active on SVs and PM, the contribution of secretion to the total auxin flux would be negligible. In conclusion, while secretory vesicle-mediated transport of auxin is an intriguing and theoretically possible model, it is unlikely to be a major mechanism of auxin transport inplanta. acknowledgement: 'European Research Council (ERC): 742985 to Jiri Friml; M.A. was supported by the Austrian Science Fund (FWF) (M2379-B28); AJ was supported by the Austria Science Fund (FWF): I03630 to Jiri Friml.' article_processing_charge: No article_type: original author: - first_name: Sander full_name: Hille, Sander last_name: Hille - first_name: Maria full_name: Akhmanova, Maria id: 3425EC26-F248-11E8-B48F-1D18A9856A87 last_name: Akhmanova orcid: 0000-0003-1522-3162 - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Alexander J full_name: Johnson, Alexander J id: 46A62C3A-F248-11E8-B48F-1D18A9856A87 last_name: Johnson orcid: 0000-0002-2739-8843 - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: 'Hille S, Akhmanova M, Glanc M, Johnson AJ, Friml J. Relative contribution of PIN-containing secretory vesicles and plasma membrane PINs to the directed auxin transport: Theoretical estimation. International Journal of Molecular Sciences. 2018;19(11). doi:10.3390/ijms19113566' apa: 'Hille, S., Akhmanova, M., Glanc, M., Johnson, A. J., & Friml, J. (2018). Relative contribution of PIN-containing secretory vesicles and plasma membrane PINs to the directed auxin transport: Theoretical estimation. International Journal of Molecular Sciences. MDPI. https://doi.org/10.3390/ijms19113566' chicago: 'Hille, Sander, Maria Akhmanova, Matous Glanc, Alexander J Johnson, and Jiří Friml. “Relative Contribution of PIN-Containing Secretory Vesicles and Plasma Membrane PINs to the Directed Auxin Transport: Theoretical Estimation.” International Journal of Molecular Sciences. MDPI, 2018. https://doi.org/10.3390/ijms19113566.' ieee: 'S. Hille, M. Akhmanova, M. Glanc, A. J. Johnson, and J. Friml, “Relative contribution of PIN-containing secretory vesicles and plasma membrane PINs to the directed auxin transport: Theoretical estimation,” International Journal of Molecular Sciences, vol. 19, no. 11. MDPI, 2018.' ista: 'Hille S, Akhmanova M, Glanc M, Johnson AJ, Friml J. 2018. Relative contribution of PIN-containing secretory vesicles and plasma membrane PINs to the directed auxin transport: Theoretical estimation. International Journal of Molecular Sciences. 19(11).' mla: 'Hille, Sander, et al. “Relative Contribution of PIN-Containing Secretory Vesicles and Plasma Membrane PINs to the Directed Auxin Transport: Theoretical Estimation.” International Journal of Molecular Sciences, vol. 19, no. 11, MDPI, 2018, doi:10.3390/ijms19113566.' short: S. Hille, M. Akhmanova, M. Glanc, A.J. Johnson, J. Friml, International Journal of Molecular Sciences 19 (2018). date_created: 2018-12-11T11:44:09Z date_published: 2018-11-12T00:00:00Z date_updated: 2023-09-18T08:09:32Z day: '12' ddc: - '580' department: - _id: DaSi - _id: JiFr doi: 10.3390/ijms19113566 ec_funded: 1 external_id: isi: - '000451528500282' file: - access_level: open_access checksum: e4b59c2599b0ca26ebf5b8434bcde94a content_type: application/pdf creator: dernst date_created: 2018-12-17T16:04:11Z date_updated: 2020-07-14T12:44:50Z file_id: '5719' file_name: 2018_IJMS_Hille.pdf file_size: 2200593 relation: main_file file_date_updated: 2020-07-14T12:44:50Z has_accepted_license: '1' intvolume: ' 19' isi: 1 issue: '11' language: - iso: eng month: '11' oa: 1 oa_version: Published Version project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants - _id: 26538374-B435-11E9-9278-68D0E5697425 call_identifier: FWF grant_number: I03630 name: Molecular mechanisms of endocytic cargo recognition in plants publication: International Journal of Molecular Sciences publication_identifier: eissn: - 1422-0067 publication_status: published publisher: MDPI publist_id: '8042' quality_controlled: '1' scopus_import: '1' status: public title: 'Relative contribution of PIN-containing secretory vesicles and plasma membrane PINs to the directed auxin transport: Theoretical estimation' tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 19 year: '2018' ... --- _id: '36' abstract: - lang: eng text: Wheat (Triticum ssp.) is one of the most important human food sources. However, this crop is very sensitive to temperature changes. Specifically, processes during wheat leaf, flower, and seed development and photosynthesis, which all contribute to the yield of this crop, are affected by high temperature. While this has to some extent been investigated on physiological, developmental, and molecular levels, very little is known about early signalling events associated with an increase in temperature. Phosphorylation-mediated signalling mechanisms, which are quick and dynamic, are associated with plant growth and development, also under abiotic stress conditions. Therefore, we probed the impact of a short-term and mild increase in temperature on the wheat leaf and spikelet phosphoproteome. In total, 3822 (containing 5178 phosphosites) and 5581 phosphopeptides (containing 7023 phosphosites) were identified in leaf and spikelet samples, respectively. Following statistical analysis, the resulting data set provides the scientific community with a first large-scale plant phosphoproteome under the control of higher ambient temperature. This community resource on the high temperature-mediated wheat phosphoproteome will be valuable for future studies. Our analyses also revealed a core set of common proteins between leaf and spikelet, suggesting some level of conserved regulatory mechanisms. Furthermore, we observed temperature-regulated interconversion of phosphoforms, which probably impacts protein activity. acknowledgement: TZ is supported by a grant from the Chinese Scholarship Council. article_processing_charge: No author: - first_name: Lam full_name: Vu, Lam last_name: Vu - first_name: Tingting full_name: Zhu, Tingting last_name: Zhu - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 - first_name: Brigitte full_name: Van De Cotte, Brigitte last_name: Van De Cotte - first_name: Kris full_name: Gevaert, Kris last_name: Gevaert - first_name: Ive full_name: De Smet, Ive last_name: De Smet citation: ama: Vu L, Zhu T, Verstraeten I, Van De Cotte B, Gevaert K, De Smet I. Temperature-induced changes in the wheat phosphoproteome reveal temperature-regulated interconversion of phosphoforms. Journal of Experimental Botany. 2018;69(19):4609-4624. doi:10.1093/jxb/ery204 apa: Vu, L., Zhu, T., Verstraeten, I., Van De Cotte, B., Gevaert, K., & De Smet, I. (2018). Temperature-induced changes in the wheat phosphoproteome reveal temperature-regulated interconversion of phosphoforms. Journal of Experimental Botany. Oxford University Press. https://doi.org/10.1093/jxb/ery204 chicago: Vu, Lam, Tingting Zhu, Inge Verstraeten, Brigitte Van De Cotte, Kris Gevaert, and Ive De Smet. “Temperature-Induced Changes in the Wheat Phosphoproteome Reveal Temperature-Regulated Interconversion of Phosphoforms.” Journal of Experimental Botany. Oxford University Press, 2018. https://doi.org/10.1093/jxb/ery204. ieee: L. Vu, T. Zhu, I. Verstraeten, B. Van De Cotte, K. Gevaert, and I. De Smet, “Temperature-induced changes in the wheat phosphoproteome reveal temperature-regulated interconversion of phosphoforms,” Journal of Experimental Botany, vol. 69, no. 19. Oxford University Press, pp. 4609–4624, 2018. ista: Vu L, Zhu T, Verstraeten I, Van De Cotte B, Gevaert K, De Smet I. 2018. Temperature-induced changes in the wheat phosphoproteome reveal temperature-regulated interconversion of phosphoforms. Journal of Experimental Botany. 69(19), 4609–4624. mla: Vu, Lam, et al. “Temperature-Induced Changes in the Wheat Phosphoproteome Reveal Temperature-Regulated Interconversion of Phosphoforms.” Journal of Experimental Botany, vol. 69, no. 19, Oxford University Press, 2018, pp. 4609–24, doi:10.1093/jxb/ery204. short: L. Vu, T. Zhu, I. Verstraeten, B. Van De Cotte, K. Gevaert, I. De Smet, Journal of Experimental Botany 69 (2018) 4609–4624. date_created: 2018-12-11T11:44:17Z date_published: 2018-08-31T00:00:00Z date_updated: 2023-09-19T10:00:46Z day: '31' ddc: - '581' department: - _id: JiFr doi: 10.1093/jxb/ery204 external_id: isi: - '000443568700010' file: - access_level: open_access checksum: 34cb0a1611588b75bd6f4913fb4e30f1 content_type: application/pdf creator: dernst date_created: 2018-12-18T09:47:51Z date_updated: 2020-07-14T12:46:13Z file_id: '5741' file_name: 2018_JournalExperimBotany_Vu.pdf file_size: 3359316 relation: main_file file_date_updated: 2020-07-14T12:46:13Z has_accepted_license: '1' intvolume: ' 69' isi: 1 issue: '19' language: - iso: eng month: '08' oa: 1 oa_version: Published Version page: 4609 - 4624 publication: Journal of Experimental Botany publication_status: published publisher: Oxford University Press publist_id: '8019' quality_controlled: '1' scopus_import: '1' status: public title: Temperature-induced changes in the wheat phosphoproteome reveal temperature-regulated interconversion of phosphoforms tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 69 year: '2018' ... --- _id: '148' abstract: - lang: eng text: 'Land plants evolved from charophytic algae, among which Charophyceae possess the most complex body plans. We present the genome of Chara braunii; comparison of the genome to those of land plants identified evolutionary novelties for plant terrestrialization and land plant heritage genes. C. braunii employs unique xylan synthases for cell wall biosynthesis, a phragmoplast (cell separation) mechanism similar to that of land plants, and many phytohormones. C. braunii plastids are controlled via land-plant-like retrograde signaling, and transcriptional regulation is more elaborate than in other algae. The morphological complexity of this organism may result from expanded gene families, with three cases of particular note: genes effecting tolerance to reactive oxygen species (ROS), LysM receptor-like kinases, and transcription factors (TFs). Transcriptomic analysis of sexual reproductive structures reveals intricate control by TFs, activity of the ROS gene network, and the ancestral use of plant-like storage and stress protection proteins in the zygote.' acknowledgement: In-Data-Review article_processing_charge: No author: - first_name: Tomoaki full_name: Nishiyama, Tomoaki last_name: Nishiyama - first_name: Hidetoshi full_name: Sakayama, Hidetoshi last_name: Sakayama - first_name: Jan full_name: De Vries, Jan last_name: De Vries - first_name: Henrik full_name: Buschmann, Henrik last_name: Buschmann - first_name: Denis full_name: Saint Marcoux, Denis last_name: Saint Marcoux - first_name: Kristian full_name: Ullrich, Kristian last_name: Ullrich - first_name: Fabian full_name: Haas, Fabian last_name: Haas - first_name: Lisa full_name: Vanderstraeten, Lisa last_name: Vanderstraeten - first_name: Dirk full_name: Becker, Dirk last_name: Becker - first_name: Daniel full_name: Lang, Daniel last_name: Lang - first_name: Stanislav full_name: Vosolsobě, Stanislav last_name: Vosolsobě - first_name: Stephane full_name: Rombauts, Stephane last_name: Rombauts - first_name: Per full_name: Wilhelmsson, Per last_name: Wilhelmsson - first_name: Philipp full_name: Janitza, Philipp last_name: Janitza - first_name: Ramona full_name: Kern, Ramona last_name: Kern - first_name: Alexander full_name: Heyl, Alexander last_name: Heyl - first_name: Florian full_name: Rümpler, Florian last_name: Rümpler - first_name: Luz full_name: Calderón Villalobos, Luz last_name: Calderón Villalobos - first_name: John full_name: Clay, John last_name: Clay - first_name: Roman full_name: Skokan, Roman last_name: Skokan - first_name: Atsushi full_name: Toyoda, Atsushi last_name: Toyoda - first_name: Yutaka full_name: Suzuki, Yutaka last_name: Suzuki - first_name: Hiroshi full_name: Kagoshima, Hiroshi last_name: Kagoshima - first_name: Elio full_name: Schijlen, Elio last_name: Schijlen - first_name: Navindra full_name: Tajeshwar, Navindra last_name: Tajeshwar - first_name: Bruno full_name: Catarino, Bruno last_name: Catarino - first_name: Alexander full_name: Hetherington, Alexander last_name: Hetherington - first_name: Assia full_name: Saltykova, Assia last_name: Saltykova - first_name: Clemence full_name: Bonnot, Clemence last_name: Bonnot - first_name: Holger full_name: Breuninger, Holger last_name: Breuninger - first_name: Aikaterini full_name: Symeonidi, Aikaterini last_name: Symeonidi - first_name: Guru full_name: Radhakrishnan, Guru last_name: Radhakrishnan - first_name: Filip full_name: Van Nieuwerburgh, Filip last_name: Van Nieuwerburgh - first_name: Dieter full_name: Deforce, Dieter last_name: Deforce - first_name: Caren full_name: Chang, Caren last_name: Chang - first_name: Kenneth full_name: Karol, Kenneth last_name: Karol - first_name: Rainer full_name: Hedrich, Rainer last_name: Hedrich - first_name: Peter full_name: Ulvskov, Peter last_name: Ulvskov - first_name: Gernot full_name: Glöckner, Gernot last_name: Glöckner - first_name: Charles full_name: Delwiche, Charles last_name: Delwiche - first_name: Jan full_name: Petrášek, Jan last_name: Petrášek - first_name: Yves full_name: Van De Peer, Yves last_name: Van De Peer - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Mary full_name: Beilby, Mary last_name: Beilby - first_name: Liam full_name: Dolan, Liam last_name: Dolan - first_name: Yuji full_name: Kohara, Yuji last_name: Kohara - first_name: Sumio full_name: Sugano, Sumio last_name: Sugano - first_name: Asao full_name: Fujiyama, Asao last_name: Fujiyama - first_name: Pierre Marc full_name: Delaux, Pierre Marc last_name: Delaux - first_name: Marcel full_name: Quint, Marcel last_name: Quint - first_name: Gunter full_name: Theissen, Gunter last_name: Theissen - first_name: Martin full_name: Hagemann, Martin last_name: Hagemann - first_name: Jesper full_name: Harholt, Jesper last_name: Harholt - first_name: Christophe full_name: Dunand, Christophe last_name: Dunand - first_name: Sabine full_name: Zachgo, Sabine last_name: Zachgo - first_name: Jane full_name: Langdale, Jane last_name: Langdale - first_name: Florian full_name: Maumus, Florian last_name: Maumus - first_name: Dominique full_name: Van Der Straeten, Dominique last_name: Van Der Straeten - first_name: Sven B full_name: Gould, Sven B last_name: Gould - first_name: Stefan full_name: Rensing, Stefan last_name: Rensing citation: ama: 'Nishiyama T, Sakayama H, De Vries J, et al. The Chara genome: Secondary complexity and implications for plant terrestrialization. Cell. 2018;174(2):448-464.e24. doi:10.1016/j.cell.2018.06.033' apa: 'Nishiyama, T., Sakayama, H., De Vries, J., Buschmann, H., Saint Marcoux, D., Ullrich, K., … Rensing, S. (2018). The Chara genome: Secondary complexity and implications for plant terrestrialization. Cell. Cell Press. https://doi.org/10.1016/j.cell.2018.06.033' chicago: 'Nishiyama, Tomoaki, Hidetoshi Sakayama, Jan De Vries, Henrik Buschmann, Denis Saint Marcoux, Kristian Ullrich, Fabian Haas, et al. “The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization.” Cell. Cell Press, 2018. https://doi.org/10.1016/j.cell.2018.06.033.' ieee: 'T. Nishiyama et al., “The Chara genome: Secondary complexity and implications for plant terrestrialization,” Cell, vol. 174, no. 2. Cell Press, p. 448–464.e24, 2018.' ista: 'Nishiyama T, Sakayama H, De Vries J, Buschmann H, Saint Marcoux D, Ullrich K, Haas F, Vanderstraeten L, Becker D, Lang D, Vosolsobě S, Rombauts S, Wilhelmsson P, Janitza P, Kern R, Heyl A, Rümpler F, Calderón Villalobos L, Clay J, Skokan R, Toyoda A, Suzuki Y, Kagoshima H, Schijlen E, Tajeshwar N, Catarino B, Hetherington A, Saltykova A, Bonnot C, Breuninger H, Symeonidi A, Radhakrishnan G, Van Nieuwerburgh F, Deforce D, Chang C, Karol K, Hedrich R, Ulvskov P, Glöckner G, Delwiche C, Petrášek J, Van De Peer Y, Friml J, Beilby M, Dolan L, Kohara Y, Sugano S, Fujiyama A, Delaux PM, Quint M, Theissen G, Hagemann M, Harholt J, Dunand C, Zachgo S, Langdale J, Maumus F, Van Der Straeten D, Gould SB, Rensing S. 2018. The Chara genome: Secondary complexity and implications for plant terrestrialization. Cell. 174(2), 448–464.e24.' mla: 'Nishiyama, Tomoaki, et al. “The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization.” Cell, vol. 174, no. 2, Cell Press, 2018, p. 448–464.e24, doi:10.1016/j.cell.2018.06.033.' short: T. Nishiyama, H. Sakayama, J. De Vries, H. Buschmann, D. Saint Marcoux, K. Ullrich, F. Haas, L. Vanderstraeten, D. Becker, D. Lang, S. Vosolsobě, S. Rombauts, P. Wilhelmsson, P. Janitza, R. Kern, A. Heyl, F. Rümpler, L. Calderón Villalobos, J. Clay, R. Skokan, A. Toyoda, Y. Suzuki, H. Kagoshima, E. Schijlen, N. Tajeshwar, B. Catarino, A. Hetherington, A. Saltykova, C. Bonnot, H. Breuninger, A. Symeonidi, G. Radhakrishnan, F. Van Nieuwerburgh, D. Deforce, C. Chang, K. Karol, R. Hedrich, P. Ulvskov, G. Glöckner, C. Delwiche, J. Petrášek, Y. Van De Peer, J. Friml, M. Beilby, L. Dolan, Y. Kohara, S. Sugano, A. Fujiyama, P.M. Delaux, M. Quint, G. Theissen, M. Hagemann, J. Harholt, C. Dunand, S. Zachgo, J. Langdale, F. Maumus, D. Van Der Straeten, S.B. Gould, S. Rensing, Cell 174 (2018) 448–464.e24. date_created: 2018-12-11T11:44:53Z date_published: 2018-07-12T00:00:00Z date_updated: 2023-09-19T10:02:47Z day: '12' department: - _id: JiFr doi: 10.1016/j.cell.2018.06.033 ec_funded: 1 external_id: isi: - '000438482800019' pmid: - '30007417' intvolume: ' 174' isi: 1 issue: '2' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pubmed/30007417 month: '07' oa: 1 oa_version: Published Version page: 448 - 464.e24 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Cell publication_status: published publisher: Cell Press publist_id: '7774' quality_controlled: '1' scopus_import: '1' status: public title: 'The Chara genome: Secondary complexity and implications for plant terrestrialization' type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 174 year: '2018' ... --- _id: '147' abstract: - lang: eng text: The trafficking of subcellular cargos in eukaryotic cells crucially depends on vesicle budding, a process mediated by ARF-GEFs (ADP-ribosylation factor guanine nucleotide exchange factors). In plants, ARF-GEFs play essential roles in endocytosis, vacuolar trafficking, recycling, secretion, and polar trafficking. Moreover, they are important for plant development, mainly through controlling the polar subcellular localization of PIN-FORMED (PIN) transporters of the plant hormone auxin. Here, using a chemical genetics screen in Arabidopsis thaliana, we identified Endosidin 4 (ES4), an inhibitor of eukaryotic ARF-GEFs. ES4 acts similarly to and synergistically with the established ARF-GEF inhibitor Brefeldin A and has broad effects on intracellular trafficking, including endocytosis, exocytosis, and vacuolar targeting. Additionally, Arabidopsis and yeast (Sacharomyces cerevisiae) mutants defective in ARF-GEF show altered sensitivity to ES4. ES4 interferes with the activation-based membrane association of the ARF1 GTPases, but not of their mutant variants that are activated independently of ARF-GEF activity. Biochemical approaches and docking simulations confirmed that ES4 specifically targets the SEC7 domain-containing ARF-GEFs. These observations collectively identify ES4 as a chemical tool enabling the study of ARF-GEF-mediated processes, including ARF-GEF-mediated plant development. acknowledgement: We thank Gerd Jürgens, Sandra Richter, and Sheng Yang He for providing antibodies; Maciek Adamowski, Fernando Aniento, Sebastian Bednarek, Nico Callewaert, Matyás Fendrych, Elena Feraru, and Mugurel I. Feraru for helpful suggestions; Siamsa Doyle for critical reading of the manuscript and helpful comments and suggestions; and Stephanie Smith and Martine De Cock for help in editing and language corrections. We acknowledge the core facility Cellular Imaging of CEITEC supported by the Czech-BioImaging large RI project (LM2015062 funded by MEYS CR) for their support with obtaining scientific data presented in this article. Plant Sciences Core Facility of CEITEC Masaryk University is gratefully acknowledged for obtaining part of the scientific data presented in this article. We acknowledge support from the Fondation pour la Recherche Médicale and from the Institut National du Cancer (J.C.). The research leading to these results was funded by the European Research Council under the European Union's 7th Framework Program (FP7/2007-2013)/ERC grant agreement numbers 282300 and 742985 and the Czech Science Foundation GAČR (GA18-26981S; J.F.); Ministry of Education, Youth, and Sports/MEYS of the Czech Republic under the Project CEITEC 2020 (LQ1601; T.N.); the China Science Council for a predoctoral fellowship (Q.L.); a joint research project within the framework of cooperation between the Research Foundation-Flanders and the Bulgarian Academy of Sciences (VS.025.13N; K.M. and E.R.); Vetenskapsrådet and Vinnova (Verket för Innovationssystem; S.R.), Knut och Alice Wallenbergs Stiftelse via “Shapesystem” Grant 2012.0050 (S.R.), Kempe stiftelserna (P.G.), Tryggers CTS410 (P.G.). article_processing_charge: No article_type: original author: - first_name: Urszula full_name: Kania, Urszula id: 4AE5C486-F248-11E8-B48F-1D18A9856A87 last_name: Kania - first_name: Tomasz full_name: Nodzyński, Tomasz last_name: Nodzyński - first_name: Qing full_name: Lu, Qing last_name: Lu - first_name: Glenn R full_name: Hicks, Glenn R last_name: Hicks - first_name: Wim full_name: Nerinckx, Wim last_name: Nerinckx - first_name: Kiril full_name: Mishev, Kiril last_name: Mishev - first_name: Francois full_name: Peurois, Francois last_name: Peurois - first_name: Jacqueline full_name: Cherfils, Jacqueline last_name: Cherfils - first_name: Rycke Riet Maria full_name: De, Rycke Riet Maria last_name: De - first_name: Peter full_name: Grones, Peter id: 399876EC-F248-11E8-B48F-1D18A9856A87 last_name: Grones - first_name: Stéphanie full_name: Robert, Stéphanie last_name: Robert - first_name: Eugenia full_name: Russinova, Eugenia last_name: Russinova - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Kania U, Nodzyński T, Lu Q, et al. The inhibitor Endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with sub cellular trafficking in eukaryotes. The Plant Cell. 2018;30(10):2553-2572. doi:10.1105/tpc.18.00127 apa: Kania, U., Nodzyński, T., Lu, Q., Hicks, G. R., Nerinckx, W., Mishev, K., … Friml, J. (2018). The inhibitor Endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with sub cellular trafficking in eukaryotes. The Plant Cell. Oxford University Press. https://doi.org/10.1105/tpc.18.00127 chicago: Kania, Urszula, Tomasz Nodzyński, Qing Lu, Glenn R Hicks, Wim Nerinckx, Kiril Mishev, Francois Peurois, et al. “The Inhibitor Endosidin 4 Targets SEC7 Domain-Type ARF GTPase Exchange Factors and Interferes with Sub Cellular Trafficking in Eukaryotes.” The Plant Cell. Oxford University Press, 2018. https://doi.org/10.1105/tpc.18.00127. ieee: U. Kania et al., “The inhibitor Endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with sub cellular trafficking in eukaryotes,” The Plant Cell, vol. 30, no. 10. Oxford University Press, pp. 2553–2572, 2018. ista: Kania U, Nodzyński T, Lu Q, Hicks GR, Nerinckx W, Mishev K, Peurois F, Cherfils J, De RRM, Grones P, Robert S, Russinova E, Friml J. 2018. The inhibitor Endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with sub cellular trafficking in eukaryotes. The Plant Cell. 30(10), 2553–2572. mla: Kania, Urszula, et al. “The Inhibitor Endosidin 4 Targets SEC7 Domain-Type ARF GTPase Exchange Factors and Interferes with Sub Cellular Trafficking in Eukaryotes.” The Plant Cell, vol. 30, no. 10, Oxford University Press, 2018, pp. 2553–72, doi:10.1105/tpc.18.00127. short: U. Kania, T. Nodzyński, Q. Lu, G.R. Hicks, W. Nerinckx, K. Mishev, F. Peurois, J. Cherfils, R.R.M. De, P. Grones, S. Robert, E. Russinova, J. Friml, The Plant Cell 30 (2018) 2553–2572. date_created: 2018-12-11T11:44:52Z date_published: 2018-11-12T00:00:00Z date_updated: 2023-09-19T10:09:12Z day: '12' department: - _id: JiFr doi: 10.1105/tpc.18.00127 ec_funded: 1 external_id: isi: - '000450000500023' pmid: - '30018156' intvolume: ' 30' isi: 1 issue: '10' language: - iso: eng main_file_link: - open_access: '1' url: https://doi.org/10.1105/tpc.18.00127 month: '11' oa: 1 oa_version: Published Version page: 2553 - 2572 pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: The Plant Cell publication_identifier: issn: - 1040-4651 publication_status: published publisher: Oxford University Press publist_id: '7776' quality_controlled: '1' scopus_import: '1' status: public title: The inhibitor Endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with sub cellular trafficking in eukaryotes type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 30 year: '2018' ... --- _id: '146' abstract: - lang: eng text: The root cap protects the stem cell niche of angiosperm roots from damage. In Arabidopsis, lateral root cap (LRC) cells covering the meristematic zone are regularly lost through programmed cell death, while the outermost layer of the root cap covering the tip is repeatedly sloughed. Efficient coordination with stem cells producing new layers is needed to maintain a constant size of the cap. We present a signalling pair, the peptide IDA-LIKE1 (IDL1) and its receptor HAESA-LIKE2 (HSL2), mediating such communication. Live imaging over several days characterized this process from initial fractures in LRC cell files to full separation of a layer. Enhanced expression of IDL1 in the separating root cap layers resulted in increased frequency of sloughing, balanced with generation of new layers in a HSL2-dependent manner. Transcriptome analyses linked IDL1-HSL2 signalling to the transcription factors BEARSKIN1/2 and genes associated with programmed cell death. Mutations in either IDL1 or HSL2 slowed down cell division, maturation and separation. Thus, IDL1-HSL2 signalling potentiates dynamic regulation of the homeostatic balance between stem cell division and sloughing activity. article_processing_charge: No article_type: original author: - first_name: Chun Lin full_name: Shi, Chun Lin last_name: Shi - first_name: Daniel full_name: Von Wangenheim, Daniel id: 49E91952-F248-11E8-B48F-1D18A9856A87 last_name: Von Wangenheim orcid: 0000-0002-6862-1247 - first_name: Ullrich full_name: Herrmann, Ullrich last_name: Herrmann - first_name: Mari full_name: Wildhagen, Mari last_name: Wildhagen - first_name: Ivan full_name: Kulik, Ivan id: F0AB3FCE-02D1-11E9-BD0E-99399A5D3DEB last_name: Kulik - first_name: Andreas full_name: Kopf, Andreas last_name: Kopf - first_name: Takashi full_name: Ishida, Takashi last_name: Ishida - first_name: Vilde full_name: Olsson, Vilde last_name: Olsson - first_name: Mari Kristine full_name: Anker, Mari Kristine last_name: Anker - first_name: Markus full_name: Albert, Markus last_name: Albert - first_name: Melinka A full_name: Butenko, Melinka A last_name: Butenko - first_name: Georg full_name: Felix, Georg last_name: Felix - first_name: Shinichiro full_name: Sawa, Shinichiro last_name: Sawa - first_name: Manfred full_name: Claassen, Manfred last_name: Claassen - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Reidunn B full_name: Aalen, Reidunn B last_name: Aalen citation: ama: Shi CL, von Wangenheim D, Herrmann U, et al. The dynamics of root cap sloughing in Arabidopsis is regulated by peptide signalling. Nature Plants. 2018;4(8):596-604. doi:10.1038/s41477-018-0212-z apa: Shi, C. L., von Wangenheim, D., Herrmann, U., Wildhagen, M., Kulik, I., Kopf, A., … Aalen, R. B. (2018). The dynamics of root cap sloughing in Arabidopsis is regulated by peptide signalling. Nature Plants. Nature Publishing Group. https://doi.org/10.1038/s41477-018-0212-z chicago: Shi, Chun Lin, Daniel von Wangenheim, Ullrich Herrmann, Mari Wildhagen, Ivan Kulik, Andreas Kopf, Takashi Ishida, et al. “The Dynamics of Root Cap Sloughing in Arabidopsis Is Regulated by Peptide Signalling.” Nature Plants. Nature Publishing Group, 2018. https://doi.org/10.1038/s41477-018-0212-z. ieee: C. L. Shi et al., “The dynamics of root cap sloughing in Arabidopsis is regulated by peptide signalling,” Nature Plants, vol. 4, no. 8. Nature Publishing Group, pp. 596–604, 2018. ista: Shi CL, von Wangenheim D, Herrmann U, Wildhagen M, Kulik I, Kopf A, Ishida T, Olsson V, Anker MK, Albert M, Butenko MA, Felix G, Sawa S, Claassen M, Friml J, Aalen RB. 2018. The dynamics of root cap sloughing in Arabidopsis is regulated by peptide signalling. Nature Plants. 4(8), 596–604. mla: Shi, Chun Lin, et al. “The Dynamics of Root Cap Sloughing in Arabidopsis Is Regulated by Peptide Signalling.” Nature Plants, vol. 4, no. 8, Nature Publishing Group, 2018, pp. 596–604, doi:10.1038/s41477-018-0212-z. short: C.L. Shi, D. von Wangenheim, U. Herrmann, M. Wildhagen, I. Kulik, A. Kopf, T. Ishida, V. Olsson, M.K. Anker, M. Albert, M.A. Butenko, G. Felix, S. Sawa, M. Claassen, J. Friml, R.B. Aalen, Nature Plants 4 (2018) 596–604. date_created: 2018-12-11T11:44:52Z date_published: 2018-07-30T00:00:00Z date_updated: 2023-09-19T10:08:45Z day: '30' ddc: - '580' department: - _id: JiFr doi: 10.1038/s41477-018-0212-z external_id: isi: - '000443861300016' pmid: - '30061750' file: - access_level: open_access checksum: da33101c76ee1b2dc5ab28fd2ccba9d0 content_type: application/pdf creator: dernst date_created: 2019-11-18T16:24:07Z date_updated: 2020-07-14T12:44:56Z file_id: '7043' file_name: 2018_NaturePlants_Shi.pdf file_size: 226829 relation: main_file file_date_updated: 2020-07-14T12:44:56Z has_accepted_license: '1' intvolume: ' 4' isi: 1 issue: '8' language: - iso: eng month: '07' oa: 1 oa_version: Submitted Version page: 596 - 604 pmid: 1 publication: Nature Plants publication_status: published publisher: Nature Publishing Group publist_id: '7777' quality_controlled: '1' related_material: link: - description: News on IST Homepage relation: press_release url: https://ist.ac.at/en/news/new-process-in-root-development-discovered/ scopus_import: '1' status: public title: The dynamics of root cap sloughing in Arabidopsis is regulated by peptide signalling type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 4 year: '2018' ... --- _id: '10881' abstract: - lang: eng text: Strigolactones (SLs) are a relatively recent addition to the list of plant hormones that control different aspects of plant development. SL signalling is perceived by an α/β hydrolase, DWARF 14 (D14). A close homolog of D14, KARRIKIN INSENSTIVE2 (KAI2), is involved in perception of an uncharacterized molecule called karrikin (KAR). Recent studies in Arabidopsis identified the SUPPRESSOR OF MAX2 1 (SMAX1) and SMAX1-LIKE 7 (SMXL7) to be potential SCF–MAX2 complex-mediated proteasome targets of KAI2 and D14, respectively. Genetic studies on SMXL7 and SMAX1 demonstrated distinct developmental roles for each, but very little is known about these repressors in terms of their sequence features. In this study, we performed an extensive comparative analysis of SMXLs and determined their phylogenetic and evolutionary history in the plant lineage. Our results show that SMXL family members can be sub-divided into four distinct phylogenetic clades/classes, with an ancient SMAX1. Further, we identified the clade-specific motifs that have evolved and that might act as determinants of SL-KAR signalling specificity. These specificities resulted from functional diversities among the clades. Our results suggest that a gradual co-evolution of SMXL members with their upstream receptors D14/KAI2 provided an increased specificity to both the SL perception and response in land plants. acknowledgement: "This project received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie Actions and it is co-financed by the South Moravian Region under grant agreement No. 665860 (SS). Access to computing and storage facilities owned by parties and projects contributing to the national grid infrastructure, MetaCentrum, provided under the program ‘Projects of Large Infrastructure for Research, Development, and Innovations’ (LM2010005) was greatly appreciated (RSV). The project was funded by The Ministry of Education, Youth and Sports/MES of the Czech Republic under the project CEITEC 2020 (LQ1601) (TN, TRM). JF was supported by the European Research Council (project ERC-2011-StG 20101109-PSDP) and the Czech Science Foundation GAČR (GA13-40637S). We thank Dr Kamel Chibani for active discussions on the evolutionary analysis and Nandan Mysore Vardarajan for his critical comments on the manuscript. This article reflects\r\nonly the authors’ views, and the EU is not responsible for any use that may be made of the information it contains. " article_processing_charge: No article_type: original author: - first_name: Taraka Ramji full_name: Moturu, Taraka Ramji last_name: Moturu - first_name: Sravankumar full_name: Thula, Sravankumar last_name: Thula - first_name: Ravi Kumar full_name: Singh, Ravi Kumar last_name: Singh - first_name: Tomasz full_name: Nodzyński, Tomasz last_name: Nodzyński - first_name: Radka Svobodová full_name: Vařeková, Radka Svobodová last_name: Vařeková - first_name: Jiří full_name: Friml, Jiří id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 - first_name: Sibu full_name: Simon, Sibu last_name: Simon citation: ama: Moturu TR, Thula S, Singh RK, et al. Molecular evolution and diversification of the SMXL gene family. Journal of Experimental Botany. 2018;69(9):2367-2378. doi:10.1093/jxb/ery097 apa: Moturu, T. R., Thula, S., Singh, R. K., Nodzyński, T., Vařeková, R. S., Friml, J., & Simon, S. (2018). Molecular evolution and diversification of the SMXL gene family. Journal of Experimental Botany. Oxford University Press. https://doi.org/10.1093/jxb/ery097 chicago: Moturu, Taraka Ramji, Sravankumar Thula, Ravi Kumar Singh, Tomasz Nodzyński, Radka Svobodová Vařeková, Jiří Friml, and Sibu Simon. “Molecular Evolution and Diversification of the SMXL Gene Family.” Journal of Experimental Botany. Oxford University Press, 2018. https://doi.org/10.1093/jxb/ery097. ieee: T. R. Moturu et al., “Molecular evolution and diversification of the SMXL gene family,” Journal of Experimental Botany, vol. 69, no. 9. Oxford University Press, pp. 2367–2378, 2018. ista: Moturu TR, Thula S, Singh RK, Nodzyński T, Vařeková RS, Friml J, Simon S. 2018. Molecular evolution and diversification of the SMXL gene family. Journal of Experimental Botany. 69(9), 2367–2378. mla: Moturu, Taraka Ramji, et al. “Molecular Evolution and Diversification of the SMXL Gene Family.” Journal of Experimental Botany, vol. 69, no. 9, Oxford University Press, 2018, pp. 2367–78, doi:10.1093/jxb/ery097. short: T.R. Moturu, S. Thula, R.K. Singh, T. Nodzyński, R.S. Vařeková, J. Friml, S. Simon, Journal of Experimental Botany 69 (2018) 2367–2378. date_created: 2022-03-18T12:43:22Z date_published: 2018-04-13T00:00:00Z date_updated: 2023-09-19T15:10:43Z day: '13' department: - _id: JiFr doi: 10.1093/jxb/ery097 ec_funded: 1 external_id: isi: - '000430727000016' pmid: - '29538714' intvolume: ' 69' isi: 1 issue: '9' keyword: - Plant Science - Physiology language: - iso: eng month: '04' oa_version: None page: 2367-2378 pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: Journal of Experimental Botany publication_identifier: eissn: - 1460-2431 issn: - 0022-0957 publication_status: published publisher: Oxford University Press quality_controlled: '1' scopus_import: '1' status: public title: Molecular evolution and diversification of the SMXL gene family type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 69 year: '2018' ... --- _id: '913' abstract: - lang: eng text: Coordinated cell polarization in developing tissues is a recurrent theme in multicellular organisms. In plants, a directional distribution of the plant hormone auxin is at the core of many developmental programs. A feedback regulation of auxin on the polarized localization of PIN auxin transporters in individual cells has been proposed as a self-organizing mechanism for coordinated tissue polarization, but the molecular mechanisms linking auxin signalling to PIN-dependent auxin transport remain unknown. We performed a microarray-based approach to find regulators of the auxin-induced PIN relocation in the Arabidopsis thaliana root. We identified a subset of a family of phosphatidylinositol transfer proteins (PITP), the PATELLINs (PATL). Here, we show that PATLs are expressed in partially overlapping cells types in different tissues going through mitosis or initiating differentiation programs. PATLs are plasma membrane-associated proteins accumulated in Arabidopsis embryos, primary roots, lateral root primordia, and developing stomata. Higher order patl mutants display reduced PIN1 repolarization in response to auxin, shorter root apical meristem, and drastic defects in embryo and seedling development. This suggests PATLs redundantly play a crucial role in polarity and patterning in Arabidopsis. article_number: jcs.204198 article_processing_charge: No author: - first_name: Ricardo full_name: Tejos, Ricardo last_name: Tejos - first_name: Cecilia full_name: Rodríguez Furlán, Cecilia last_name: Rodríguez Furlán - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Michael full_name: Sauer, Michael last_name: Sauer - first_name: Lorena full_name: Norambuena, Lorena last_name: Norambuena - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Tejos R, Rodríguez Furlán C, Adamowski M, Sauer M, Norambuena L, Friml J. PATELLINS are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis thaliana. Journal of Cell Science. 2018;131(2). doi:10.1242/jcs.204198 apa: Tejos, R., Rodríguez Furlán, C., Adamowski, M., Sauer, M., Norambuena, L., & Friml, J. (2018). PATELLINS are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis thaliana. Journal of Cell Science. Company of Biologists. https://doi.org/10.1242/jcs.204198 chicago: Tejos, Ricardo, Cecilia Rodríguez Furlán, Maciek Adamowski, Michael Sauer, Lorena Norambuena, and Jiří Friml. “PATELLINS Are Regulators of Auxin Mediated PIN1 Relocation and Plant Development in Arabidopsis Thaliana.” Journal of Cell Science. Company of Biologists, 2018. https://doi.org/10.1242/jcs.204198. ieee: R. Tejos, C. Rodríguez Furlán, M. Adamowski, M. Sauer, L. Norambuena, and J. Friml, “PATELLINS are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis thaliana,” Journal of Cell Science, vol. 131, no. 2. Company of Biologists, 2018. ista: Tejos R, Rodríguez Furlán C, Adamowski M, Sauer M, Norambuena L, Friml J. 2018. PATELLINS are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis thaliana. Journal of Cell Science. 131(2), jcs. 204198. mla: Tejos, Ricardo, et al. “PATELLINS Are Regulators of Auxin Mediated PIN1 Relocation and Plant Development in Arabidopsis Thaliana.” Journal of Cell Science, vol. 131, no. 2, jcs. 204198, Company of Biologists, 2018, doi:10.1242/jcs.204198. short: R. Tejos, C. Rodríguez Furlán, M. Adamowski, M. Sauer, L. Norambuena, J. Friml, Journal of Cell Science 131 (2018). date_created: 2018-12-11T11:49:10Z date_published: 2018-01-29T00:00:00Z date_updated: 2023-09-26T15:47:50Z day: '29' ddc: - '581' department: - _id: JiFr doi: 10.1242/jcs.204198 ec_funded: 1 external_id: isi: - '000424842400019' file: - access_level: open_access checksum: bf156c20a4f117b4b932370d54cbac8c content_type: application/pdf creator: dernst date_created: 2019-04-12T08:46:32Z date_updated: 2020-07-14T12:48:15Z file_id: '6299' file_name: 2017_adamowski_PATELLINS_are.pdf file_size: 14925985 relation: main_file file_date_updated: 2020-07-14T12:48:15Z has_accepted_license: '1' intvolume: ' 131' isi: 1 issue: '2' language: - iso: eng month: '01' oa: 1 oa_version: Published Version project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: Journal of Cell Science publication_identifier: issn: - '00219533' publication_status: published publisher: Company of Biologists publist_id: '6530' pubrep_id: '988' quality_controlled: '1' scopus_import: '1' status: public title: PATELLINS are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis thaliana type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 131 year: '2018' ... --- _id: '5673' abstract: - lang: eng text: Cell polarity, manifested by the localization of proteins to distinct polar plasma membrane domains, is a key prerequisite of multicellular life. In plants, PIN auxin transporters are prominent polarity markers crucial for a plethora of developmental processes. Cell polarity mechanisms in plants are distinct from other eukaryotes and still largely elusive. In particular, how the cell polarities are propagated and maintained following cell division remains unknown. Plant cytokinesis is orchestrated by the cell plate—a transient centrifugally growing endomembrane compartment ultimately forming the cross wall1. Trafficking of polar membrane proteins is typically redirected to the cell plate, and these will consequently have opposite polarity in at least one of the daughter cells2–5. Here, we provide mechanistic insights into post-cytokinetic re-establishment of cell polarity as manifested by the apical, polar localization of PIN2. We show that the apical domain is defined in a cell-intrinsic manner and that re-establishment of PIN2 localization to this domain requires de novo protein secretion and endocytosis, but not basal-to-apical transcytosis. Furthermore, we identify a PINOID-related kinase WAG1, which phosphorylates PIN2 in vitro6 and is transcriptionally upregulated specifically in dividing cells, as a crucial regulator of post-cytokinetic PIN2 polarity re-establishment. article_processing_charge: No author: - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Glanc M, Fendrych M, Friml J. Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division. Nature Plants. 2018;4(12):1082-1088. doi:10.1038/s41477-018-0318-3 apa: Glanc, M., Fendrych, M., & Friml, J. (2018). Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division. Nature Plants. Nature Research. https://doi.org/10.1038/s41477-018-0318-3 chicago: Glanc, Matous, Matyas Fendrych, and Jiří Friml. “Mechanistic Framework for Cell-Intrinsic Re-Establishment of PIN2 Polarity after Cell Division.” Nature Plants. Nature Research, 2018. https://doi.org/10.1038/s41477-018-0318-3. ieee: M. Glanc, M. Fendrych, and J. Friml, “Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division,” Nature Plants, vol. 4, no. 12. Nature Research, pp. 1082–1088, 2018. ista: Glanc M, Fendrych M, Friml J. 2018. Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division. Nature Plants. 4(12), 1082–1088. mla: Glanc, Matous, et al. “Mechanistic Framework for Cell-Intrinsic Re-Establishment of PIN2 Polarity after Cell Division.” Nature Plants, vol. 4, no. 12, Nature Research, 2018, pp. 1082–88, doi:10.1038/s41477-018-0318-3. short: M. Glanc, M. Fendrych, J. Friml, Nature Plants 4 (2018) 1082–1088. date_created: 2018-12-16T22:59:18Z date_published: 2018-12-03T00:00:00Z date_updated: 2023-10-17T12:19:28Z day: '03' department: - _id: JiFr doi: 10.1038/s41477-018-0318-3 ec_funded: 1 external_id: isi: - '000454576600017' pmid: - '30518833' intvolume: ' 4' isi: 1 issue: '12' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pubmed/30518833 month: '12' oa: 1 oa_version: Submitted Version page: 1082-1088 pmid: 1 project: - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Nature Plants publication_identifier: issn: - 2055-0278 publication_status: published publisher: Nature Research quality_controlled: '1' scopus_import: '1' status: public title: Mechanistic framework for cell-intrinsic re-establishment of PIN2 polarity after cell division type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 4 year: '2018' ... --- _id: '412' abstract: - lang: eng text: Clathrin-mediated endocytosis (CME) is a cellular trafficking process in which cargoes and lipids are internalized from the plasma membrane into vesicles coated with clathrin and adaptor proteins. CME is essential for many developmental and physiological processes in plants, but its underlying mechanism is not well characterised compared to that in yeast and animal systems. Here, we searched for new factors involved in CME in Arabidopsis thaliana by performing Tandem Affinity Purification of proteins that interact with clathrin light chain, a principal component of the clathrin coat. Among the confirmed interactors, we found two putative homologues of the clathrin-coat uncoating factor auxilin previously described in non-plant systems. Overexpression of AUXILIN-LIKE1 and AUXILIN-LIKE2 in A. thaliana caused an arrest of seedling growth and development. This was concomitant with inhibited endocytosis due to blocking of clathrin recruitment after the initial step of adaptor protein binding to the plasma membrane. By contrast, auxilin-like(1/2) loss-of-function lines did not present endocytosis-related developmental or cellular phenotypes under normal growth conditions. This work contributes to the on-going characterization of the endocytotic machinery in plants and provides a robust tool for conditionally and specifically interfering with CME in A. thaliana. acknowledgement: We thank James Matthew Watson, Monika Borowska, and Peggy Stolt-Bergner at ProTech Facility of the Vienna Biocenter Core Facilities for the CRISPR/CAS9 construct; Anna Müller for assistance with molecular cloning; Sebastian Bednarek, Liwen Jiang, and Daniël Van Damme for sharing published material; Matyáš Fendrych, Daniël Van Damme, and Lindy Abas for valuable discussions; and Martine De Cock for help with correcting the manuscript. This work was supported by the European Research Council under the European Union Seventh Framework Programme (FP7/2007-2013)/ERC Grant 282300 and by the Ministry of Education of the Czech Republic/MŠMT project NPUI-LO1417. article_processing_charge: No article_type: original author: - first_name: Maciek full_name: Adamowski, Maciek id: 45F536D2-F248-11E8-B48F-1D18A9856A87 last_name: Adamowski orcid: 0000-0001-6463-5257 - first_name: Madhumitha full_name: Narasimhan, Madhumitha id: 44BF24D0-F248-11E8-B48F-1D18A9856A87 last_name: Narasimhan orcid: 0000-0002-8600-0671 - first_name: Urszula full_name: Kania, Urszula id: 4AE5C486-F248-11E8-B48F-1D18A9856A87 last_name: Kania - first_name: Matous full_name: Glanc, Matous id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2 last_name: Glanc orcid: 0000-0003-0619-7783 - first_name: Geert full_name: De Jaeger, Geert last_name: De Jaeger - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Adamowski M, Narasimhan M, Kania U, Glanc M, De Jaeger G, Friml J. A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis. The Plant Cell. 2018;30(3):700-716. doi:10.1105/tpc.17.00785 apa: Adamowski, M., Narasimhan, M., Kania, U., Glanc, M., De Jaeger, G., & Friml, J. (2018). A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis. The Plant Cell. American Society of Plant Biologists. https://doi.org/10.1105/tpc.17.00785 chicago: Adamowski, Maciek, Madhumitha Narasimhan, Urszula Kania, Matous Glanc, Geert De Jaeger, and Jiří Friml. “A Functional Study of AUXILIN LIKE1 and 2 Two Putative Clathrin Uncoating Factors in Arabidopsis.” The Plant Cell. American Society of Plant Biologists, 2018. https://doi.org/10.1105/tpc.17.00785. ieee: M. Adamowski, M. Narasimhan, U. Kania, M. Glanc, G. De Jaeger, and J. Friml, “A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis,” The Plant Cell, vol. 30, no. 3. American Society of Plant Biologists, pp. 700–716, 2018. ista: Adamowski M, Narasimhan M, Kania U, Glanc M, De Jaeger G, Friml J. 2018. A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis. The Plant Cell. 30(3), 700–716. mla: Adamowski, Maciek, et al. “A Functional Study of AUXILIN LIKE1 and 2 Two Putative Clathrin Uncoating Factors in Arabidopsis.” The Plant Cell, vol. 30, no. 3, American Society of Plant Biologists, 2018, pp. 700–16, doi:10.1105/tpc.17.00785. short: M. Adamowski, M. Narasimhan, U. Kania, M. Glanc, G. De Jaeger, J. Friml, The Plant Cell 30 (2018) 700–716. date_created: 2018-12-11T11:46:20Z date_published: 2018-04-09T00:00:00Z date_updated: 2024-03-27T23:30:06Z day: '09' ddc: - '580' department: - _id: JiFr doi: 10.1105/tpc.17.00785 ec_funded: 1 external_id: isi: - '000429441400018' pmid: - '29511054' file: - access_level: open_access checksum: 4e165e653b67d3f0684697f21aace5a1 content_type: application/pdf creator: dernst date_created: 2022-05-23T09:12:38Z date_updated: 2022-05-23T09:12:38Z file_id: '11406' file_name: 2018_PlantCell_Adamowski.pdf file_size: 4407538 relation: main_file success: 1 file_date_updated: 2022-05-23T09:12:38Z has_accepted_license: '1' intvolume: ' 30' isi: 1 issue: '3' language: - iso: eng month: '04' oa: 1 oa_version: Published Version page: 700 - 716 pmid: 1 project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: The Plant Cell publication_identifier: eissn: - 1532-298X issn: - 1040-4651 publication_status: published publisher: American Society of Plant Biologists publist_id: '7417' quality_controlled: '1' related_material: record: - id: '6269' relation: dissertation_contains status: public scopus_import: '1' status: public title: A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 30 year: '2018' ... --- _id: '449' abstract: - lang: eng text: Auxin is unique among plant hormones due to its directional transport that is mediated by the polarly distributed PIN auxin transporters at the plasma membrane. The canalization hypothesis proposes that the auxin feedback on its polar flow is a crucial, plant-specific mechanism mediating multiple self-organizing developmental processes. Here, we used the auxin effect on the PIN polar localization in Arabidopsis thaliana roots as a proxy for the auxin feedback on the PIN polarity during canalization. We performed microarray experiments to find regulators of this process that act downstream of auxin. We identified genes that were transcriptionally regulated by auxin in an AXR3/IAA17- and ARF7/ARF19-dependent manner. Besides the known components of the PIN polarity, such as PID and PIP5K kinases, a number of potential new regulators were detected, among which the WRKY23 transcription factor, which was characterized in more detail. Gain- and loss-of-function mutants confirmed a role for WRKY23 in mediating the auxin effect on the PIN polarity. Accordingly, processes requiring auxin-mediated PIN polarity rearrangements, such as vascular tissue development during leaf venation, showed a higher WRKY23 expression and required the WRKY23 activity. Our results provide initial insights into the auxin transcriptional network acting upstream of PIN polarization and, potentially, canalization-mediated plant development. article_processing_charge: Yes author: - first_name: Tomas full_name: Prat, Tomas id: 3DA3BFEE-F248-11E8-B48F-1D18A9856A87 last_name: Prat - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Wim full_name: Grunewald, Wim last_name: Grunewald - first_name: Mina K full_name: Vasileva, Mina K id: 3407EB18-F248-11E8-B48F-1D18A9856A87 last_name: Vasileva - first_name: Gergely full_name: Molnar, Gergely id: 34F1AF46-F248-11E8-B48F-1D18A9856A87 last_name: Molnar - first_name: Ricardo full_name: Tejos, Ricardo last_name: Tejos - first_name: Markus full_name: Schmid, Markus last_name: Schmid - first_name: Michael full_name: Sauer, Michael last_name: Sauer - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Prat T, Hajny J, Grunewald W, et al. WRKY23 is a component of the transcriptional network mediating auxin feedback on PIN polarity. PLoS Genetics. 2018;14(1). doi:10.1371/journal.pgen.1007177 apa: Prat, T., Hajny, J., Grunewald, W., Vasileva, M. K., Molnar, G., Tejos, R., … Friml, J. (2018). WRKY23 is a component of the transcriptional network mediating auxin feedback on PIN polarity. PLoS Genetics. Public Library of Science. https://doi.org/10.1371/journal.pgen.1007177 chicago: Prat, Tomas, Jakub Hajny, Wim Grunewald, Mina K Vasileva, Gergely Molnar, Ricardo Tejos, Markus Schmid, Michael Sauer, and Jiří Friml. “WRKY23 Is a Component of the Transcriptional Network Mediating Auxin Feedback on PIN Polarity.” PLoS Genetics. Public Library of Science, 2018. https://doi.org/10.1371/journal.pgen.1007177. ieee: T. Prat et al., “WRKY23 is a component of the transcriptional network mediating auxin feedback on PIN polarity,” PLoS Genetics, vol. 14, no. 1. Public Library of Science, 2018. ista: Prat T, Hajny J, Grunewald W, Vasileva MK, Molnar G, Tejos R, Schmid M, Sauer M, Friml J. 2018. WRKY23 is a component of the transcriptional network mediating auxin feedback on PIN polarity. PLoS Genetics. 14(1). mla: Prat, Tomas, et al. “WRKY23 Is a Component of the Transcriptional Network Mediating Auxin Feedback on PIN Polarity.” PLoS Genetics, vol. 14, no. 1, Public Library of Science, 2018, doi:10.1371/journal.pgen.1007177. short: T. Prat, J. Hajny, W. Grunewald, M.K. Vasileva, G. Molnar, R. Tejos, M. Schmid, M. Sauer, J. Friml, PLoS Genetics 14 (2018). date_created: 2018-12-11T11:46:32Z date_published: 2018-01-29T00:00:00Z date_updated: 2024-03-27T23:30:37Z day: '29' ddc: - '581' department: - _id: JiFr doi: 10.1371/journal.pgen.1007177 ec_funded: 1 external_id: isi: - '000423718600034' file: - access_level: open_access checksum: 0276d66788ec076f4924164a39e6a712 content_type: application/pdf creator: system date_created: 2018-12-12T10:10:52Z date_updated: 2020-07-14T12:46:30Z file_id: '4843' file_name: IST-2018-967-v1+1_journal.pgen.1007177.pdf file_size: 24709062 relation: main_file file_date_updated: 2020-07-14T12:46:30Z has_accepted_license: '1' intvolume: ' 14' isi: 1 issue: '1' language: - iso: eng month: '01' oa: 1 oa_version: Published Version project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants publication: PLoS Genetics publication_status: published publisher: Public Library of Science publist_id: '7373' pubrep_id: '967' quality_controlled: '1' related_material: record: - id: '1127' relation: dissertation_contains status: public - id: '7172' relation: dissertation_contains status: public - id: '8822' relation: dissertation_contains status: public scopus_import: '1' status: public title: WRKY23 is a component of the transcriptional network mediating auxin feedback on PIN polarity tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 14 year: '2018' ... --- _id: '191' abstract: - lang: eng text: Intercellular distribution of the plant hormone auxin largely depends on the polar subcellular distribution of the plasma membrane PIN-FORMED (PIN) auxin transporters. PIN polarity switches in response to different developmental and environmental signals have been shown to redirect auxin fluxes mediating certain developmental responses. PIN phosphorylation at different sites and by different kinases is crucial for PIN function. Here we investigate the role of PIN phosphorylation during gravitropic response. Loss- and gain-of-function mutants in PINOID and related kinases but not in D6PK kinase as well as mutations mimicking constitutive dephosphorylated or phosphorylated status of two clusters of predicted phosphorylation sites partially disrupted PIN3 phosphorylation and caused defects in gravitropic bending in roots and hypocotyls. In particular, they impacted PIN3 polarity rearrangements in response to gravity and during feed-back regulation by auxin itself. Thus PIN phosphorylation, besides regulating transport activity and apical-basal targeting, is also important for the rapid polarity switches in response to environmental and endogenous signals. article_number: '10279' article_processing_charge: No author: - first_name: Peter full_name: Grones, Peter id: 399876EC-F248-11E8-B48F-1D18A9856A87 last_name: Grones - first_name: Melinda F full_name: Abas, Melinda F id: 3CFB3B1C-F248-11E8-B48F-1D18A9856A87 last_name: Abas - first_name: Jakub full_name: Hajny, Jakub id: 4800CC20-F248-11E8-B48F-1D18A9856A87 last_name: Hajny orcid: 0000-0003-2140-7195 - first_name: Angharad full_name: Jones, Angharad last_name: Jones - first_name: Sascha full_name: Waidmann, Sascha last_name: Waidmann - first_name: Jürgen full_name: Kleine Vehn, Jürgen last_name: Kleine Vehn - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Grones P, Abas MF, Hajny J, et al. PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism. Scientific Reports. 2018;8(1). doi:10.1038/s41598-018-28188-1 apa: Grones, P., Abas, M. F., Hajny, J., Jones, A., Waidmann, S., Kleine Vehn, J., & Friml, J. (2018). PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism. Scientific Reports. Springer. https://doi.org/10.1038/s41598-018-28188-1 chicago: Grones, Peter, Melinda F Abas, Jakub Hajny, Angharad Jones, Sascha Waidmann, Jürgen Kleine Vehn, and Jiří Friml. “PID/WAG-Mediated Phosphorylation of the Arabidopsis PIN3 Auxin Transporter Mediates Polarity Switches during Gravitropism.” Scientific Reports. Springer, 2018. https://doi.org/10.1038/s41598-018-28188-1. ieee: P. Grones et al., “PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism,” Scientific Reports, vol. 8, no. 1. Springer, 2018. ista: Grones P, Abas MF, Hajny J, Jones A, Waidmann S, Kleine Vehn J, Friml J. 2018. PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism. Scientific Reports. 8(1), 10279. mla: Grones, Peter, et al. “PID/WAG-Mediated Phosphorylation of the Arabidopsis PIN3 Auxin Transporter Mediates Polarity Switches during Gravitropism.” Scientific Reports, vol. 8, no. 1, 10279, Springer, 2018, doi:10.1038/s41598-018-28188-1. short: P. Grones, M.F. Abas, J. Hajny, A. Jones, S. Waidmann, J. Kleine Vehn, J. Friml, Scientific Reports 8 (2018). date_created: 2018-12-11T11:45:06Z date_published: 2018-07-06T00:00:00Z date_updated: 2024-03-27T23:30:37Z day: '06' ddc: - '581' department: - _id: JiFr - _id: EvBe doi: 10.1038/s41598-018-28188-1 ec_funded: 1 external_id: isi: - '000437673200053' file: - access_level: open_access checksum: 266b03f4fb8198e83141617aaa99dcab content_type: application/pdf creator: dernst date_created: 2018-12-17T15:38:56Z date_updated: 2020-07-14T12:45:20Z file_id: '5714' file_name: 2018_ScientificReports_Grones.pdf file_size: 2413876 relation: main_file file_date_updated: 2020-07-14T12:45:20Z has_accepted_license: '1' intvolume: ' 8' isi: 1 issue: '1' language: - iso: eng month: '07' oa: 1 oa_version: Published Version project: - _id: 25716A02-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '282300' name: Polarity and subcellular dynamics in plants - _id: 261099A6-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '742985' name: Tracing Evolution of Auxin Transport and Polarity in Plants publication: Scientific Reports publication_status: published publisher: Springer publist_id: '7729' quality_controlled: '1' related_material: record: - id: '8822' relation: dissertation_contains status: public scopus_import: '1' status: public title: PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1 volume: 8 year: '2018' ... --- _id: '442' abstract: - lang: eng text: The rapid auxin-triggered growth of the Arabidopsis hypocotyls involves the nuclear TIR1/AFB-Aux/IAA signaling and is accompanied by acidification of the apoplast and cell walls (Fendrych et al., 2016). Here, we describe in detail the method for analysis of the elongation and the TIR1/AFB-Aux/IAA-dependent auxin response in hypocotyl segments as well as the determination of relative values of the cell wall pH. acknowledgement: 'This protocol was adapted from Fendrych et al., 2016. This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie Grant Agreement No. 665385, and Austrian Science Fund (FWF) [M 2128-B21]. ' article_processing_charge: No article_type: original author: - first_name: Lanxin full_name: Li, Lanxin id: 367EF8FA-F248-11E8-B48F-1D18A9856A87 last_name: Li orcid: 0000-0002-5607-272X - first_name: Gabriel full_name: Krens, Gabriel id: 2B819732-F248-11E8-B48F-1D18A9856A87 last_name: Krens orcid: 0000-0003-4761-5996 - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Jirí full_name: Friml, Jirí id: 4159519E-F248-11E8-B48F-1D18A9856A87 last_name: Friml orcid: 0000-0002-8302-7596 citation: ama: Li L, Krens G, Fendrych M, Friml J. Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls. Bio-protocol. 2018;8(1). doi:10.21769/BioProtoc.2685 apa: Li, L., Krens, G., Fendrych, M., & Friml, J. (2018). Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls. Bio-Protocol. Bio-protocol. https://doi.org/10.21769/BioProtoc.2685 chicago: Li, Lanxin, Gabriel Krens, Matyas Fendrych, and Jiří Friml. “Real-Time Analysis of Auxin Response, Cell Wall PH and Elongation in Arabidopsis Thaliana Hypocotyls.” Bio-Protocol. Bio-protocol, 2018. https://doi.org/10.21769/BioProtoc.2685. ieee: L. Li, G. Krens, M. Fendrych, and J. Friml, “Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls,” Bio-protocol, vol. 8, no. 1. Bio-protocol, 2018. ista: Li L, Krens G, Fendrych M, Friml J. 2018. Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls. Bio-protocol. 8(1). mla: Li, Lanxin, et al. “Real-Time Analysis of Auxin Response, Cell Wall PH and Elongation in Arabidopsis Thaliana Hypocotyls.” Bio-Protocol, vol. 8, no. 1, Bio-protocol, 2018, doi:10.21769/BioProtoc.2685. short: L. Li, G. Krens, M. Fendrych, J. Friml, Bio-Protocol 8 (2018). date_created: 2018-12-11T11:46:30Z date_published: 2018-01-05T00:00:00Z date_updated: 2024-03-27T23:30:42Z day: '05' ddc: - '576' - '581' department: - _id: JiFr - _id: Bio doi: 10.21769/BioProtoc.2685 ec_funded: 1 file: - access_level: open_access checksum: 6644ba698206eda32b0abf09128e63e3 content_type: application/pdf creator: system date_created: 2018-12-12T10:17:43Z date_updated: 2020-07-14T12:46:29Z file_id: '5299' file_name: IST-2018-970-v1+1_2018_Lanxin_Real-time_analysis.pdf file_size: 11352389 relation: main_file file_date_updated: 2020-07-14T12:46:29Z has_accepted_license: '1' intvolume: ' 8' issue: '1' language: - iso: eng month: '01' oa: 1 oa_version: Published Version project: - _id: 2564DBCA-B435-11E9-9278-68D0E5697425 call_identifier: H2020 grant_number: '665385' name: International IST Doctoral Program publication: Bio-protocol publication_identifier: eissn: - 2331-8325 publication_status: published publisher: Bio-protocol publist_id: '7381' pubrep_id: '970' quality_controlled: '1' related_material: record: - id: '10083' relation: dissertation_contains status: public status: public title: Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 8 year: '2018' ... --- _id: '572' abstract: - lang: eng text: In this review, we summarize the different biosynthesis-related pathways that contribute to the regulation of endogenous auxin in plants. We demonstrate that all known genes involved in auxin biosynthesis also have a role in root formation, from the initiation of a root meristem during embryogenesis to the generation of a functional root system with a primary root, secondary lateral root branches and adventitious roots. Furthermore, the versatile adaptation of root development in response to environmental challenges is mediated by both local and distant control of auxin biosynthesis. In conclusion, auxin homeostasis mediated by spatial and temporal regulation of auxin biosynthesis plays a central role in determining root architecture. article_number: '2587' article_processing_charge: No author: - first_name: Damilola full_name: Olatunji, Damilola last_name: Olatunji - first_name: Danny full_name: Geelen, Danny last_name: Geelen - first_name: Inge full_name: Verstraeten, Inge id: 362BF7FE-F248-11E8-B48F-1D18A9856A87 last_name: Verstraeten orcid: 0000-0001-7241-2328 citation: ama: Olatunji D, Geelen D, Verstraeten I. Control of endogenous auxin levels in plant root development. International Journal of Molecular Sciences. 2017;18(12). doi:10.3390/ijms18122587 apa: Olatunji, D., Geelen, D., & Verstraeten, I. (2017). Control of endogenous auxin levels in plant root development. International Journal of Molecular Sciences. MDPI. https://doi.org/10.3390/ijms18122587 chicago: Olatunji, Damilola, Danny Geelen, and Inge Verstraeten. “Control of Endogenous Auxin Levels in Plant Root Development.” International Journal of Molecular Sciences. MDPI, 2017. https://doi.org/10.3390/ijms18122587. ieee: D. Olatunji, D. Geelen, and I. Verstraeten, “Control of endogenous auxin levels in plant root development,” International Journal of Molecular Sciences, vol. 18, no. 12. MDPI, 2017. ista: Olatunji D, Geelen D, Verstraeten I. 2017. Control of endogenous auxin levels in plant root development. International Journal of Molecular Sciences. 18(12), 2587. mla: Olatunji, Damilola, et al. “Control of Endogenous Auxin Levels in Plant Root Development.” International Journal of Molecular Sciences, vol. 18, no. 12, 2587, MDPI, 2017, doi:10.3390/ijms18122587. short: D. Olatunji, D. Geelen, I. Verstraeten, International Journal of Molecular Sciences 18 (2017). date_created: 2018-12-11T11:47:15Z date_published: 2017-12-01T00:00:00Z date_updated: 2021-01-12T08:03:16Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.3390/ijms18122587 file: - access_level: open_access checksum: 82d51f11e493f7eec02976d9a9a9805e content_type: application/pdf creator: system date_created: 2018-12-12T10:08:55Z date_updated: 2020-07-14T12:47:10Z file_id: '4718' file_name: IST-2017-917-v1+1_ijms-18-02587.pdf file_size: 920962 relation: main_file file_date_updated: 2020-07-14T12:47:10Z has_accepted_license: '1' intvolume: ' 18' issue: '12' language: - iso: eng month: '12' oa: 1 oa_version: Published Version publication: International Journal of Molecular Sciences publication_status: published publisher: MDPI publist_id: '7242' pubrep_id: '917' quality_controlled: '1' scopus_import: '1' status: public title: Control of endogenous auxin levels in plant root development tmp: image: /images/cc_by.png legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) short: CC BY (4.0) type: journal_article user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87 volume: 18 year: '2017' ... --- _id: '657' abstract: - lang: eng text: Plant organs are typically organized into three main tissue layers. The middle ground tissue layer comprises the majority of the plant body and serves a wide range of functions, including photosynthesis, selective nutrient uptake and storage, and gravity sensing. Ground tissue patterning and maintenance in Arabidopsis are controlled by a well-established gene network revolving around the key regulator SHORT-ROOT (SHR). In contrast, it is completely unknown how ground tissue identity is first specified from totipotent precursor cells in the embryo. The plant signaling molecule auxin, acting through AUXIN RESPONSE FACTOR (ARF) transcription factors, is critical for embryo patterning. The auxin effector ARF5/MONOPTEROS (MP) acts both cell-autonomously and noncell-autonomously to control embryonic vascular tissue formation and root initiation, respectively. Here we show that auxin response and ARF activity cell-autonomously control the asymmetric division of the first ground tissue cells. By identifying embryonic target genes, we show that MP transcriptionally initiates the ground tissue lineage and acts upstream of the regulatory network that controls ground tissue patterning and maintenance. Strikingly, whereas the SHR network depends on MP, this MP function is, at least in part, SHR independent. Our study therefore identifies auxin response as a regulator of ground tissue specification in the embryonic root, and reveals that ground tissue initiation and maintenance use different regulators and mechanisms. Moreover, our data provide a framework for the simultaneous formation of multiple cell types by the same transcriptional regulator. author: - first_name: Barbara full_name: Möller, Barbara last_name: Möller - first_name: Colette full_name: Ten Hove, Colette last_name: Ten Hove - first_name: Daoquan full_name: Xiang, Daoquan last_name: Xiang - first_name: Nerys full_name: Williams, Nerys last_name: Williams - first_name: Lorena full_name: López, Lorena last_name: López - first_name: Saiko full_name: Yoshida, Saiko id: 2E46069C-F248-11E8-B48F-1D18A9856A87 last_name: Yoshida - first_name: Margot full_name: Smit, Margot last_name: Smit - first_name: Raju full_name: Datla, Raju last_name: Datla - first_name: Dolf full_name: Weijers, Dolf last_name: Weijers citation: ama: Möller B, Ten Hove C, Xiang D, et al. Auxin response cell autonomously controls ground tissue initiation in the early arabidopsis embryo. PNAS. 2017;114(12):E2533-E2539. doi:10.1073/pnas.1616493114 apa: Möller, B., Ten Hove, C., Xiang, D., Williams, N., López, L., Yoshida, S., … Weijers, D. (2017). Auxin response cell autonomously controls ground tissue initiation in the early arabidopsis embryo. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1616493114 chicago: Möller, Barbara, Colette Ten Hove, Daoquan Xiang, Nerys Williams, Lorena López, Saiko Yoshida, Margot Smit, Raju Datla, and Dolf Weijers. “Auxin Response Cell Autonomously Controls Ground Tissue Initiation in the Early Arabidopsis Embryo.” PNAS. National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1616493114. ieee: B. Möller et al., “Auxin response cell autonomously controls ground tissue initiation in the early arabidopsis embryo,” PNAS, vol. 114, no. 12. National Academy of Sciences, pp. E2533–E2539, 2017. ista: Möller B, Ten Hove C, Xiang D, Williams N, López L, Yoshida S, Smit M, Datla R, Weijers D. 2017. Auxin response cell autonomously controls ground tissue initiation in the early arabidopsis embryo. PNAS. 114(12), E2533–E2539. mla: Möller, Barbara, et al. “Auxin Response Cell Autonomously Controls Ground Tissue Initiation in the Early Arabidopsis Embryo.” PNAS, vol. 114, no. 12, National Academy of Sciences, 2017, pp. E2533–39, doi:10.1073/pnas.1616493114. short: B. Möller, C. Ten Hove, D. Xiang, N. Williams, L. López, S. Yoshida, M. Smit, R. Datla, D. Weijers, PNAS 114 (2017) E2533–E2539. date_created: 2018-12-11T11:47:45Z date_published: 2017-03-21T00:00:00Z date_updated: 2021-01-12T08:08:02Z day: '21' department: - _id: JiFr doi: 10.1073/pnas.1616493114 external_id: pmid: - '28265057' intvolume: ' 114' issue: '12' language: - iso: eng main_file_link: - open_access: '1' url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373392/ month: '03' oa: 1 oa_version: Submitted Version page: E2533 - E2539 pmid: 1 publication: PNAS publication_identifier: issn: - '00278424' publication_status: published publisher: National Academy of Sciences publist_id: '7076' quality_controlled: '1' scopus_import: 1 status: public title: Auxin response cell autonomously controls ground tissue initiation in the early arabidopsis embryo type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 114 year: '2017' ... --- _id: '669' abstract: - lang: eng text: 'The exocyst, a eukaryotic tethering complex, coregulates targeted exocytosis as an effector of small GTPases in polarized cell growth. In land plants, several exocyst subunits are encoded by double or triple paralogs, culminating in tens of EXO70 paralogs. Out of 23 Arabidopsis thaliana EXO70 isoforms, we analyzed seven isoforms expressed in pollen. Genetic and microscopic analyses of single mutants in EXO70A2, EXO70C1, EXO70C2, EXO70F1, EXO70H3, EXO70H5, and EXO70H6 genes revealed that only a loss-of-function EXO70C2 allele resulted in a significant male-specific transmission defect (segregation 40%:51%:9%) due to aberrant pollen tube growth. Mutant pollen tubes grown in vitro exhibited an enhanced growth rate and a decreased thickness of the tip cell wall, causing tip bursts. However, exo70C2 pollen tubes could frequently recover and restart their speedy elongation, resulting in a repetitive stop-and-go growth dynamics. A pollenspecific depletion of the closest paralog, EXO70C1, using artificial microRNA in the exo70C2 mutant background, resulted in a complete pollen-specific transmission defect, suggesting redundant functions of EXO70C1 and EXO70C2. Both EXO70C1 and EXO70C2, GFP tagged and expressed under the control of their native promoters, localized in the cytoplasm of pollen grains, pollen tubes, and also root trichoblast cells. The expression of EXO70C2-GFP complemented the aberrant growth of exo70C2 pollen tubes. The absent EXO70C2 interactions with core exocyst subunits in the yeast two-hybrid assay, cytoplasmic localization, and genetic effect suggest an unconventional EXO70 function possibly as a regulator of exocytosis outside the exocyst complex. In conclusion, EXO70C2 is a novel factor contributing to the regulation of optimal tip growth of Arabidopsis pollen tubes. ' article_processing_charge: No article_type: original author: - first_name: Lukáš full_name: Synek, Lukáš last_name: Synek - first_name: Nemanja full_name: Vukašinović, Nemanja last_name: Vukašinović - first_name: Ivan full_name: Kulich, Ivan last_name: Kulich - first_name: Michal full_name: Hála, Michal last_name: Hála - first_name: Klára full_name: Aldorfová, Klára last_name: Aldorfová - first_name: Matyas full_name: Fendrych, Matyas id: 43905548-F248-11E8-B48F-1D18A9856A87 last_name: Fendrych orcid: 0000-0002-9767-8699 - first_name: Viktor full_name: Žárský, Viktor last_name: Žárský citation: ama: Synek L, Vukašinović N, Kulich I, et al. EXO70C2 is a key regulatory factor for optimal tip growth of pollen. Plant Physiology. 2017;174(1):223-240. doi:10.1104/pp.16.01282 apa: Synek, L., Vukašinović, N., Kulich, I., Hála, M., Aldorfová, K., Fendrych, M., & Žárský, V. (2017). EXO70C2 is a key regulatory factor for optimal tip growth of pollen. Plant Physiology. American Society of Plant Biologists. https://doi.org/10.1104/pp.16.01282 chicago: Synek, Lukáš, Nemanja Vukašinović, Ivan Kulich, Michal Hála, Klára Aldorfová, Matyas Fendrych, and Viktor Žárský. “EXO70C2 Is a Key Regulatory Factor for Optimal Tip Growth of Pollen.” Plant Physiology. American Society of Plant Biologists, 2017. https://doi.org/10.1104/pp.16.01282. ieee: L. Synek et al., “EXO70C2 is a key regulatory factor for optimal tip growth of pollen,” Plant Physiology, vol. 174, no. 1. American Society of Plant Biologists, pp. 223–240, 2017. ista: Synek L, Vukašinović N, Kulich I, Hála M, Aldorfová K, Fendrych M, Žárský V. 2017. EXO70C2 is a key regulatory factor for optimal tip growth of pollen. Plant Physiology. 174(1), 223–240. mla: Synek, Lukáš, et al. “EXO70C2 Is a Key Regulatory Factor for Optimal Tip Growth of Pollen.” Plant Physiology, vol. 174, no. 1, American Society of Plant Biologists, 2017, pp. 223–40, doi:10.1104/pp.16.01282. short: L. Synek, N. Vukašinović, I. Kulich, M. Hála, K. Aldorfová, M. Fendrych, V. Žárský, Plant Physiology 174 (2017) 223–240. date_created: 2018-12-11T11:47:49Z date_published: 2017-05-01T00:00:00Z date_updated: 2021-01-12T08:08:35Z day: '01' ddc: - '580' department: - _id: JiFr doi: 10.1104/pp.16.01282 external_id: pmid: - '28356503' file: - access_level: open_access checksum: 97155acc6aa5f0d0a78e0589a932fe02 content_type: application/pdf creator: dernst date_created: 2019-11-18T16:16:18Z date_updated: 2020-07-14T12:47:37Z file_id: '7041' file_name: 2017_PlantPhysio_Synek.pdf file_size: 2176903 relation: main_file file_date_updated: 2020-07-14T12:47:37Z has_accepted_license: '1' intvolume: ' 174' issue: '1' language: - iso: eng month: '05' oa: 1 oa_version: Submitted Version page: 223 - 240 pmid: 1 publication: Plant Physiology publication_identifier: issn: - '00320889' publication_status: published publisher: American Society of Plant Biologists publist_id: '7058' quality_controlled: '1' scopus_import: 1 status: public title: EXO70C2 is a key regulatory factor for optimal tip growth of pollen type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 174 year: '2017' ... --- _id: '722' abstract: - lang: eng text: Plants are sessile organisms rooted in one place. The soil resources that plants require are often distributed in a highly heterogeneous pattern. To aid foraging, plants have evolved roots whose growth and development are highly responsive to soil signals. As a result, 3D root architecture is shaped by myriad environmental signals to ensure resource capture is optimised and unfavourable environments are avoided. The first signals sensed by newly germinating seeds — gravity and light — direct root growth into the soil to aid seedling establishment. Heterogeneous soil resources, such as water, nitrogen and phosphate, also act as signals that shape 3D root growth to optimise uptake. Root architecture is also modified through biotic interactions that include soil fungi and neighbouring plants. This developmental plasticity results in a ‘custom-made’ 3D root system that is best adapted to forage for resources in each soil environment that a plant colonises. author: - first_name: Emily full_name: Morris, Emily last_name: Morris - first_name: Marcus full_name: Griffiths, Marcus last_name: Griffiths - first_name: Agata full_name: Golebiowska, Agata last_name: Golebiowska - first_name: Stefan full_name: Mairhofer, Stefan last_name: Mairhofer - first_name: Jasmine full_name: Burr Hersey, Jasmine last_name: Burr Hersey - first_name: Tatsuaki full_name: Goh, Tatsuaki last_name: Goh - first_name: Daniel full_name: Von Wangenheim, Daniel id: 49E91952-F248-11E8-B48F-1D18A9856A87 last_name: Von Wangenheim orcid: 0000-0002-6862-1247 - first_name: Brian full_name: Atkinson, Brian last_name: Atkinson - first_name: Craig full_name: Sturrock, Craig last_name: Sturrock - first_name: Jonathan full_name: Lynch, Jonathan last_name: Lynch - first_name: Kris full_name: Vissenberg, Kris last_name: Vissenberg - first_name: Karl full_name: Ritz, Karl last_name: Ritz - first_name: Darren full_name: Wells, Darren last_name: Wells - first_name: Sacha full_name: Mooney, Sacha last_name: Mooney - first_name: Malcolm full_name: Bennett, Malcolm last_name: Bennett citation: ama: Morris E, Griffiths M, Golebiowska A, et al. Shaping 3D root system architecture. Current Biology. 2017;27(17):R919-R930. doi:10.1016/j.cub.2017.06.043 apa: Morris, E., Griffiths, M., Golebiowska, A., Mairhofer, S., Burr Hersey, J., Goh, T., … Bennett, M. (2017). Shaping 3D root system architecture. Current Biology. Cell Press. https://doi.org/10.1016/j.cub.2017.06.043 chicago: Morris, Emily, Marcus Griffiths, Agata Golebiowska, Stefan Mairhofer, Jasmine Burr Hersey, Tatsuaki Goh, Daniel von Wangenheim, et al. “Shaping 3D Root System Architecture.” Current Biology. Cell Press, 2017. https://doi.org/10.1016/j.cub.2017.06.043. ieee: E. Morris et al., “Shaping 3D root system architecture,” Current Biology, vol. 27, no. 17. Cell Press, pp. R919–R930, 2017. ista: Morris E, Griffiths M, Golebiowska A, Mairhofer S, Burr Hersey J, Goh T, von Wangenheim D, Atkinson B, Sturrock C, Lynch J, Vissenberg K, Ritz K, Wells D, Mooney S, Bennett M. 2017. Shaping 3D root system architecture. Current Biology. 27(17), R919–R930. mla: Morris, Emily, et al. “Shaping 3D Root System Architecture.” Current Biology, vol. 27, no. 17, Cell Press, 2017, pp. R919–30, doi:10.1016/j.cub.2017.06.043. short: E. Morris, M. Griffiths, A. Golebiowska, S. Mairhofer, J. Burr Hersey, T. Goh, D. von Wangenheim, B. Atkinson, C. Sturrock, J. Lynch, K. Vissenberg, K. Ritz, D. Wells, S. Mooney, M. Bennett, Current Biology 27 (2017) R919–R930. date_created: 2018-12-11T11:48:08Z date_published: 2017-09-11T00:00:00Z date_updated: 2021-01-12T08:12:29Z day: '11' ddc: - '581' department: - _id: JiFr doi: 10.1016/j.cub.2017.06.043 ec_funded: 1 external_id: pmid: - '28898665' file: - access_level: open_access checksum: e45588b21097b408da6276a3e5eedb2e content_type: application/pdf creator: dernst date_created: 2019-04-17T07:46:40Z date_updated: 2020-07-14T12:47:54Z file_id: '6332' file_name: 2017_CurrentBiology_Morris.pdf file_size: 1576593 relation: main_file file_date_updated: 2020-07-14T12:47:54Z has_accepted_license: '1' intvolume: ' 27' issue: '17' language: - iso: eng month: '09' oa: 1 oa_version: Submitted Version page: R919 - R930 pmid: 1 project: - _id: 25681D80-B435-11E9-9278-68D0E5697425 call_identifier: FP7 grant_number: '291734' name: International IST Postdoc Fellowship Programme publication: Current Biology publication_identifier: issn: - '09609822' publication_status: published publisher: Cell Press publist_id: '6956' pubrep_id: '982' quality_controlled: '1' scopus_import: 1 status: public title: Shaping 3D root system architecture tmp: image: /images/cc_by_nc_nd.png legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) short: CC BY-NC-ND (4.0) type: journal_article user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87 volume: 27 year: '2017' ...