---
_id: '1383'
abstract:
- lang: eng
  text: In plants, vacuolar H+-ATPase (V-ATPase) activity acidifies both the trans-Golgi
    network/early endosome (TGN/EE) and the vacuole. This dual V-ATPase function has
    impeded our understanding of how the pH homeostasis within the plant TGN/EE controls
    exo- and endocytosis. Here, we show that the weak V-ATPase mutant deetiolated3
    (det3) displayed a pH increase in the TGN/EE, but not in the vacuole, strongly
    impairing secretion and recycling of the brassinosteroid receptor and the cellulose
    synthase complexes to the plasma membrane, in contrast to mutants lacking tonoplast-localized
    V-ATPase activity only. The brassinosteroid insensitivity and the cellulose deficiency
    defects in det3 were tightly correlated with reduced Golgi and TGN/EE motility.
    Thus, our results provide strong evidence that acidification of the TGN/EE, but
    not of the vacuole, is indispensable for functional secretion and recycling in
    plants.
article_number: '15094'
article_processing_charge: No
article_type: original
author:
- first_name: Luo
  full_name: Yu, Luo
  last_name: Yu
- first_name: Stefan
  full_name: Scholl, Stefan
  last_name: Scholl
- first_name: Anett
  full_name: Doering, Anett
  last_name: Doering
- first_name: Zhang
  full_name: Yi, Zhang
  last_name: Yi
- first_name: Niloufer
  full_name: Irani, Niloufer
  last_name: Irani
- first_name: Simone
  full_name: Di Rubbo, Simone
  last_name: Di Rubbo
- first_name: Lutz
  full_name: Neumetzler, Lutz
  last_name: Neumetzler
- first_name: Praveen
  full_name: Krishnamoorthy, Praveen
  last_name: Krishnamoorthy
- first_name: Isabelle
  full_name: Van Houtte, Isabelle
  last_name: Van Houtte
- first_name: Evelien
  full_name: Mylle, Evelien
  last_name: Mylle
- first_name: Volker
  full_name: Bischoff, Volker
  last_name: Bischoff
- first_name: Samantha
  full_name: Vernhettes, Samantha
  last_name: Vernhettes
- first_name: Johan
  full_name: Winne, Johan
  last_name: Winne
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: York
  full_name: Stierhof, York
  last_name: Stierhof
- first_name: Karin
  full_name: Schumacher, Karin
  last_name: Schumacher
- first_name: Staffan
  full_name: Persson, Staffan
  last_name: Persson
- first_name: Eugenia
  full_name: Russinova, Eugenia
  last_name: Russinova
citation:
  ama: Yu L, Scholl S, Doering A, et al. V-ATPase activity in the TGN/EE is required
    for exocytosis and recycling in Arabidopsis. <i>Nature Plants</i>. 2015;1(7).
    doi:<a href="https://doi.org/10.1038/nplants.2015.94">10.1038/nplants.2015.94</a>
  apa: Yu, L., Scholl, S., Doering, A., Yi, Z., Irani, N., Di Rubbo, S., … Russinova,
    E. (2015). V-ATPase activity in the TGN/EE is required for exocytosis and recycling
    in Arabidopsis. <i>Nature Plants</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nplants.2015.94">https://doi.org/10.1038/nplants.2015.94</a>
  chicago: Yu, Luo, Stefan Scholl, Anett Doering, Zhang Yi, Niloufer Irani, Simone
    Di Rubbo, Lutz Neumetzler, et al. “V-ATPase Activity in the TGN/EE Is Required
    for Exocytosis and Recycling in Arabidopsis.” <i>Nature Plants</i>. Nature Publishing
    Group, 2015. <a href="https://doi.org/10.1038/nplants.2015.94">https://doi.org/10.1038/nplants.2015.94</a>.
  ieee: L. Yu <i>et al.</i>, “V-ATPase activity in the TGN/EE is required for exocytosis
    and recycling in Arabidopsis,” <i>Nature Plants</i>, vol. 1, no. 7. Nature Publishing
    Group, 2015.
  ista: Yu L, Scholl S, Doering A, Yi Z, Irani N, Di Rubbo S, Neumetzler L, Krishnamoorthy
    P, Van Houtte I, Mylle E, Bischoff V, Vernhettes S, Winne J, Friml J, Stierhof
    Y, Schumacher K, Persson S, Russinova E. 2015. V-ATPase activity in the TGN/EE
    is required for exocytosis and recycling in Arabidopsis. Nature Plants. 1(7),
    15094.
  mla: Yu, Luo, et al. “V-ATPase Activity in the TGN/EE Is Required for Exocytosis
    and Recycling in Arabidopsis.” <i>Nature Plants</i>, vol. 1, no. 7, 15094, Nature
    Publishing Group, 2015, doi:<a href="https://doi.org/10.1038/nplants.2015.94">10.1038/nplants.2015.94</a>.
  short: L. Yu, S. Scholl, A. Doering, Z. Yi, N. Irani, S. Di Rubbo, L. Neumetzler,
    P. Krishnamoorthy, I. Van Houtte, E. Mylle, V. Bischoff, S. Vernhettes, J. Winne,
    J. Friml, Y. Stierhof, K. Schumacher, S. Persson, E. Russinova, Nature Plants
    1 (2015).
date_created: 2018-12-11T11:51:42Z
date_published: 2015-07-06T00:00:00Z
date_updated: 2025-09-29T11:04:05Z
day: '06'
department:
- _id: JiFr
doi: 10.1038/nplants.2015.94
external_id:
  isi:
  - '000364407200001'
  pmid:
  - '27250258'
intvolume: '         1'
isi: 1
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905525/
month: '07'
oa: 1
oa_version: Submitted Version
pmid: 1
publication: Nature Plants
publication_status: published
publisher: Nature Publishing Group
publist_id: '5827'
quality_controlled: '1'
scopus_import: '1'
status: public
title: V-ATPase activity in the TGN/EE is required for exocytosis and recycling in
  Arabidopsis
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 1
year: '2015'
...
---
_id: '1509'
abstract:
- lang: eng
  text: The Auxin Binding Protein1 (ABP1) has been identified based on its ability
    to bind auxin with high affinity and studied for a long time as a prime candidate
    for the extracellular auxin receptor responsible for mediating in particular the
    fast non-transcriptional auxin responses. However, the contradiction between the
    embryo-lethal phenotypes of the originally described Arabidopsis T-DNA insertional
    knock-out alleles (abp1-1 and abp1-1s) and the wild type-like phenotypes of other
    recently described loss-of-function alleles (abp1-c1 and abp1-TD1) questions the
    biological importance of ABP1 and relevance of the previous genetic studies. Here
    we show that there is no hidden copy of the ABP1 gene in the Arabidopsis genome
    but the embryo-lethal phenotypes of abp1-1 and abp1-1s alleles are very similar
    to the knock-out phenotypes of the neighboring gene, BELAYA SMERT (BSM). Furthermore,
    the allelic complementation test between bsm and abp1 alleles shows that the embryo-lethality
    in the abp1-1 and abp1-1s alleles is caused by the off-target disruption of the
    BSM locus by the T-DNA insertions. This clarifies the controversy of different
    phenotypes among published abp1 knock-out alleles and asks for reflections on
    the developmental role of ABP1.
acknowledgement: "This work was supported by ERC Independent Research grant (ERC-2011-StG-20101109-PSDP
  to JF). JM internship was supported by the grant “Action Austria – Slovakia”.\r\nData
  associated with the article are available under the terms of the Creative Commons
  Zero \"No rights reserved\" data waiver (CC0 1.0 Public domain dedication). \r\n\r\nData
  availability: \r\nF1000Research: Dataset 1. Dataset 1, 10.5256/f1000research.7143.d104552\r\n\r\nF1000Research:
  Dataset 2. Dataset 2, 10.5256/f1000research.7143.d104553\r\n\r\nF1000Research: Dataset
  3. Dataset 3, 10.5256/f1000research.7143.d104554"
article_processing_charge: No
author:
- first_name: Jaroslav
  full_name: Michalko, Jaroslav
  id: 483727CA-F248-11E8-B48F-1D18A9856A87
  last_name: Michalko
- first_name: Marta
  full_name: Dravecka, Marta
  id: 4342E402-F248-11E8-B48F-1D18A9856A87
  last_name: Dravecka
  orcid: 0000-0002-2519-8004
- first_name: Tobias
  full_name: Bollenbach, Tobias
  id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
  last_name: Bollenbach
  orcid: 0000-0003-4398-476X
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Michalko J, Lukacisinova M, Bollenbach MT, Friml J. Embryo-lethal phenotypes
    in early abp1 mutants are due to disruption of the neighboring BSM gene. <i>F1000
    Research </i>. 2015;4. doi:<a href="https://doi.org/10.12688/f1000research.7143.1">10.12688/f1000research.7143.1</a>
  apa: Michalko, J., Lukacisinova, M., Bollenbach, M. T., &#38; Friml, J. (2015).
    Embryo-lethal phenotypes in early abp1 mutants are due to disruption of the neighboring
    BSM gene. <i>F1000 Research </i>. F1000 Research. <a href="https://doi.org/10.12688/f1000research.7143.1">https://doi.org/10.12688/f1000research.7143.1</a>
  chicago: Michalko, Jaroslav, Marta Lukacisinova, Mark Tobias Bollenbach, and Jiří
    Friml. “Embryo-Lethal Phenotypes in Early Abp1 Mutants Are Due to Disruption of
    the Neighboring BSM Gene.” <i>F1000 Research </i>. F1000 Research, 2015. <a href="https://doi.org/10.12688/f1000research.7143.1">https://doi.org/10.12688/f1000research.7143.1</a>.
  ieee: J. Michalko, M. Lukacisinova, M. T. Bollenbach, and J. Friml, “Embryo-lethal
    phenotypes in early abp1 mutants are due to disruption of the neighboring BSM
    gene,” <i>F1000 Research </i>, vol. 4. F1000 Research, 2015.
  ista: Michalko J, Lukacisinova M, Bollenbach MT, Friml J. 2015. Embryo-lethal phenotypes
    in early abp1 mutants are due to disruption of the neighboring BSM gene. F1000
    Research . 4.
  mla: Michalko, Jaroslav, et al. “Embryo-Lethal Phenotypes in Early Abp1 Mutants
    Are Due to Disruption of the Neighboring BSM Gene.” <i>F1000 Research </i>, vol.
    4, F1000 Research, 2015, doi:<a href="https://doi.org/10.12688/f1000research.7143.1">10.12688/f1000research.7143.1</a>.
  short: J. Michalko, M. Lukacisinova, M.T. Bollenbach, J. Friml, F1000 Research  4
    (2015).
corr_author: '1'
date_created: 2018-12-11T11:52:26Z
date_published: 2015-10-01T00:00:00Z
date_updated: 2025-04-15T07:48:03Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
- _id: ToBo
doi: 10.12688/f1000research.7143.1
ec_funded: 1
file:
- access_level: open_access
  checksum: 8beae5cbe988e1060265ae7de2ee8306
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:16:12Z
  date_updated: 2020-07-14T12:44:59Z
  file_id: '5198'
  file_name: IST-2016-497-v1+1_10.12688_f1000research.7143.1_20151102.pdf
  file_size: 4414248
  relation: main_file
file_date_updated: 2020-07-14T12:44:59Z
has_accepted_license: '1'
intvolume: '         4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '10'
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: 'F1000 Research '
publication_status: published
publisher: F1000 Research
publist_id: '5668'
pubrep_id: '497'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Embryo-lethal phenotypes in early abp1 mutants are due to disruption of the
  neighboring BSM gene
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: 4
year: '2015'
...
---
_id: '1532'
abstract:
- lang: eng
  text: Ammonium is the major nitrogen source in some plant ecosystems but is toxic
    at high concentrations, especially when available as the exclusive nitrogen source.
    Ammonium stress rapidly leads to various metabolic and hormonal imbalances that
    ultimately inhibit root and shoot growth in many plant species, including Arabidopsis
    thaliana (L.) Heynh. To identify molecular and genetic factors involved in seedling
    survival with prolonged exclusive NH4+ nutrition, a transcriptomic analysis with
    microarrays was used. Substantial transcriptional differences were most pronounced
    in (NH4)2SO4-grown seedlings, compared with plants grown on KNO3 or NH4NO3. Consistent
    with previous physiological analyses, major differences in the expression modules
    of photosynthesis-related genes, an altered mitochondrial metabolism, differential
    expression of the primary NH4+ assimilation, alteration of transporter gene expression
    and crucial changes in cell wall biosynthesis were found. A major difference in
    plant hormone responses, particularly of auxin but not cytokinin, was striking.
    The activity of the DR5::GUS reporter revealed a dramatically decreased auxin
    response in (NH4)2SO4-grown primary roots. The impaired root growth on (NH4)2SO4
    was partially rescued by exogenous auxin or in specific mutants in the auxin pathway.
    The data suggest that NH4+-induced nutritional and metabolic imbalances can be
    partially overcome by elevated auxin levels.
article_processing_charge: No
article_type: original
author:
- first_name: Huaiyu
  full_name: Yang, Huaiyu
  last_name: Yang
- first_name: Jenny
  full_name: Von Der Fecht Bartenbach, Jenny
  last_name: Von Der Fecht Bartenbach
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jan
  full_name: Lohmann, Jan
  last_name: Lohmann
- first_name: Benjamin
  full_name: Neuhäuser, Benjamin
  last_name: Neuhäuser
- first_name: Uwe
  full_name: Ludewig, Uwe
  last_name: Ludewig
citation:
  ama: Yang H, Von Der Fecht Bartenbach J, Friml J, Lohmann J, Neuhäuser B, Ludewig
    U. Auxin-modulated root growth inhibition in Arabidopsis thaliana seedlings with
    ammonium as the sole nitrogen source. <i>Functional Plant Biology</i>. 2015;42(3):239-251.
    doi:<a href="https://doi.org/10.1071/FP14171">10.1071/FP14171</a>
  apa: Yang, H., Von Der Fecht Bartenbach, J., Friml, J., Lohmann, J., Neuhäuser,
    B., &#38; Ludewig, U. (2015). Auxin-modulated root growth inhibition in Arabidopsis
    thaliana seedlings with ammonium as the sole nitrogen source. <i>Functional Plant
    Biology</i>. CSIRO. <a href="https://doi.org/10.1071/FP14171">https://doi.org/10.1071/FP14171</a>
  chicago: Yang, Huaiyu, Jenny Von Der Fecht Bartenbach, Jiří Friml, Jan Lohmann,
    Benjamin Neuhäuser, and Uwe Ludewig. “Auxin-Modulated Root Growth Inhibition in
    Arabidopsis Thaliana Seedlings with Ammonium as the Sole Nitrogen Source.” <i>Functional
    Plant Biology</i>. CSIRO, 2015. <a href="https://doi.org/10.1071/FP14171">https://doi.org/10.1071/FP14171</a>.
  ieee: H. Yang, J. Von Der Fecht Bartenbach, J. Friml, J. Lohmann, B. Neuhäuser,
    and U. Ludewig, “Auxin-modulated root growth inhibition in Arabidopsis thaliana
    seedlings with ammonium as the sole nitrogen source,” <i>Functional Plant Biology</i>,
    vol. 42, no. 3. CSIRO, pp. 239–251, 2015.
  ista: Yang H, Von Der Fecht Bartenbach J, Friml J, Lohmann J, Neuhäuser B, Ludewig
    U. 2015. Auxin-modulated root growth inhibition in Arabidopsis thaliana seedlings
    with ammonium as the sole nitrogen source. Functional Plant Biology. 42(3), 239–251.
  mla: Yang, Huaiyu, et al. “Auxin-Modulated Root Growth Inhibition in Arabidopsis
    Thaliana Seedlings with Ammonium as the Sole Nitrogen Source.” <i>Functional Plant
    Biology</i>, vol. 42, no. 3, CSIRO, 2015, pp. 239–51, doi:<a href="https://doi.org/10.1071/FP14171">10.1071/FP14171</a>.
  short: H. Yang, J. Von Der Fecht Bartenbach, J. Friml, J. Lohmann, B. Neuhäuser,
    U. Ludewig, Functional Plant Biology 42 (2015) 239–251.
date_created: 2018-12-11T11:52:34Z
date_published: 2015-03-01T00:00:00Z
date_updated: 2025-09-23T07:59:44Z
day: '01'
department:
- _id: JiFr
doi: 10.1071/FP14171
external_id:
  isi:
  - '000349635900003'
  pmid:
  - '32480670'
intvolume: '        42'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa_version: None
page: 239 - 251
pmid: 1
publication: Functional Plant Biology
publication_identifier:
  issn:
  - 1445-4408
publication_status: published
publisher: CSIRO
publist_id: '5639'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Auxin-modulated root growth inhibition in Arabidopsis thaliana seedlings with
  ammonium as the sole nitrogen source
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 42
year: '2015'
...
---
_id: '1534'
abstract:
- lang: eng
  text: PIN proteins are auxin export carriers that direct intercellular auxin flow
    and in turn regulate many aspects of plant growth and development including responses
    to environmental changes. The Arabidopsis R2R3-MYB transcription factor FOUR LIPS
    (FLP) and its paralogue MYB88 regulate terminal divisions during stomatal development,
    as well as female reproductive development and stress responses. Here we show
    that FLP and MYB88 act redundantly but differentially in regulating the transcription
    of PIN3 and PIN7 in gravity-sensing cells of primary and lateral roots. On the
    one hand, FLP is involved in responses to gravity stimulation in primary roots,
    whereas on the other, FLP and MYB88 function complementarily in establishing the
    gravitropic set-point angles of lateral roots. Our results support a model in
    which FLP and MYB88 expression specifically determines the temporal-spatial patterns
    of PIN3 and PIN7 transcription that are closely associated with their preferential
    functions during root responses to gravity.
article_number: '8822'
article_processing_charge: No
author:
- first_name: Hongzhe
  full_name: Wang, Hongzhe
  last_name: Wang
- first_name: Kezhen
  full_name: Yang, Kezhen
  last_name: Yang
- first_name: Junjie
  full_name: Zou, Junjie
  last_name: Zou
- first_name: Lingling
  full_name: Zhu, Lingling
  last_name: Zhu
- first_name: Zidian
  full_name: Xie, Zidian
  last_name: Xie
- first_name: Miyoterao
  full_name: Morita, Miyoterao
  last_name: Morita
- first_name: Masao
  full_name: Tasaka, Masao
  last_name: Tasaka
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Erich
  full_name: Grotewold, Erich
  last_name: Grotewold
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Fred
  full_name: Sack, Fred
  last_name: Sack
- first_name: Jie
  full_name: Le, Jie
  last_name: Le
citation:
  ama: Wang H, Yang K, Zou J, et al. Transcriptional regulation of PIN genes by FOUR
    LIPS and MYB88 during Arabidopsis root gravitropism. <i>Nature Communications</i>.
    2015;6. doi:<a href="https://doi.org/10.1038/ncomms9822">10.1038/ncomms9822</a>
  apa: Wang, H., Yang, K., Zou, J., Zhu, L., Xie, Z., Morita, M., … Le, J. (2015).
    Transcriptional regulation of PIN genes by FOUR LIPS and MYB88 during Arabidopsis
    root gravitropism. <i>Nature Communications</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/ncomms9822">https://doi.org/10.1038/ncomms9822</a>
  chicago: Wang, Hongzhe, Kezhen Yang, Junjie Zou, Lingling Zhu, Zidian Xie, Miyoterao
    Morita, Masao Tasaka, et al. “Transcriptional Regulation of PIN Genes by FOUR
    LIPS and MYB88 during Arabidopsis Root Gravitropism.” <i>Nature Communications</i>.
    Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/ncomms9822">https://doi.org/10.1038/ncomms9822</a>.
  ieee: H. Wang <i>et al.</i>, “Transcriptional regulation of PIN genes by FOUR LIPS
    and MYB88 during Arabidopsis root gravitropism,” <i>Nature Communications</i>,
    vol. 6. Nature Publishing Group, 2015.
  ista: Wang H, Yang K, Zou J, Zhu L, Xie Z, Morita M, Tasaka M, Friml J, Grotewold
    E, Beeckman T, Vanneste S, Sack F, Le J. 2015. Transcriptional regulation of PIN
    genes by FOUR LIPS and MYB88 during Arabidopsis root gravitropism. Nature Communications.
    6, 8822.
  mla: Wang, Hongzhe, et al. “Transcriptional Regulation of PIN Genes by FOUR LIPS
    and MYB88 during Arabidopsis Root Gravitropism.” <i>Nature Communications</i>,
    vol. 6, 8822, Nature Publishing Group, 2015, doi:<a href="https://doi.org/10.1038/ncomms9822">10.1038/ncomms9822</a>.
  short: H. Wang, K. Yang, J. Zou, L. Zhu, Z. Xie, M. Morita, M. Tasaka, J. Friml,
    E. Grotewold, T. Beeckman, S. Vanneste, F. Sack, J. Le, Nature Communications
    6 (2015).
date_created: 2018-12-11T11:52:34Z
date_published: 2015-11-18T00:00:00Z
date_updated: 2025-09-23T14:55:59Z
day: '18'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1038/ncomms9822
ec_funded: 1
external_id:
  isi:
  - '000366295500008'
file:
- access_level: open_access
  checksum: 3c06735fc7cd7e482ca830cbd26001bf
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:07Z
  date_updated: 2020-07-14T12:45:01Z
  file_id: '5259'
  file_name: IST-2016-485-v1+1_ncomms9822.pdf
  file_size: 1852268
  relation: main_file
file_date_updated: 2020-07-14T12:45:01Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '11'
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: Nature Communications
publication_status: published
publisher: Nature Publishing Group
publist_id: '5637'
pubrep_id: '485'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Transcriptional regulation of PIN genes by FOUR LIPS and MYB88 during Arabidopsis
  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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 6
year: '2015'
...
---
_id: '1536'
abstract:
- lang: eng
  text: Strigolactones, first discovered as germination stimulants for parasitic weeds
    [1], are carotenoid-derived phytohormones that play major roles in inhibiting
    lateral bud outgrowth and promoting plant-mycorrhizal symbiosis [2-4]. Furthermore,
    strigolactones are involved in the regulation of lateral and adventitious root
    development, root cell division [5, 6], secondary growth [7], and leaf senescence
    [8]. Recently, we discovered the strigolactone transporter Petunia axillaris PLEIOTROPIC
    DRUG RESISTANCE 1 (PaPDR1), which is required for efficient mycorrhizal colonization
    and inhibition of lateral bud outgrowth [9]. However, how strigolactones are transported
    through the plant remained unknown. Here we show that PaPDR1 exhibits a cell-type-specific
    asymmetric localization in different root tissues. In root tips, PaPDR1 is co-expressed
    with the strigolactone biosynthetic gene DAD1 (CCD8), and it is localized at the
    apical membrane of root hypodermal cells, presumably mediating the shootward transport
    of strigolactone. Above the root tip, in the hypodermal passage cells that form
    gates for the entry of mycorrhizal fungi, PaPDR1 is present in the outer-lateral
    membrane, compatible with its postulated function as strigolactone exporter from
    root to soil. Transport studies are in line with our localization studies since
    (1) a papdr1 mutant displays impaired transport of strigolactones out of the root
    tip to the shoot as well as into the rhizosphere and (2) DAD1 expression and PIN1/PIN2
    levels change in plants deregulated for PDR1 expression, suggestive of variations
    in endogenous strigolactone contents. In conclusion, our results indicate that
    the polar localizations of PaPDR1 mediate directional shootward strigolactone
    transport as well as localized exudation into the soil.
acknowledgement: "This work was funded by a grant of the Swiss National Foundation
  to E.M.\r\nWe thank Dr. José María Mateos (University of Zurich) for providing us
  with the vibratome, Prof. Dolf Weijers (Wageningen University, the Netherlands)
  for shipping us his set of ligation-independent cloning vectors, Prof. Bruno Humbel
  (University of Lausanne) for suggestions on GFP-PDR1 detection, and Dr. Undine Krügel
  (University of Zurich) and Prof. Michal Jasinski (Polish Academy of Science) for
  hints on protein quantification."
article_processing_charge: No
author:
- first_name: Joëlle
  full_name: Sasse, Joëlle
  last_name: Sasse
- first_name: Sibu
  full_name: Simon, Sibu
  id: 4542EF9A-F248-11E8-B48F-1D18A9856A87
  last_name: Simon
  orcid: 0000-0002-1998-6741
- first_name: Christian
  full_name: Gübeli, Christian
  last_name: Gübeli
- first_name: Guowei
  full_name: Liu, Guowei
  last_name: Liu
- first_name: Xi
  full_name: Cheng, Xi
  last_name: Cheng
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Harro
  full_name: Bouwmeester, Harro
  last_name: Bouwmeester
- first_name: Enrico
  full_name: Martinoia, Enrico
  last_name: Martinoia
- first_name: Lorenzo
  full_name: Borghi, Lorenzo
  last_name: Borghi
citation:
  ama: Sasse J, Simon S, Gübeli C, et al. Asymmetric localizations of the ABC transporter
    PaPDR1 trace paths of directional strigolactone transport. <i>Current Biology</i>.
    2015;25(5):647-655. doi:<a href="https://doi.org/10.1016/j.cub.2015.01.015">10.1016/j.cub.2015.01.015</a>
  apa: Sasse, J., Simon, S., Gübeli, C., Liu, G., Cheng, X., Friml, J., … Borghi,
    L. (2015). Asymmetric localizations of the ABC transporter PaPDR1 trace paths
    of directional strigolactone transport. <i>Current Biology</i>. Cell Press. <a
    href="https://doi.org/10.1016/j.cub.2015.01.015">https://doi.org/10.1016/j.cub.2015.01.015</a>
  chicago: Sasse, Joëlle, Sibu Simon, Christian Gübeli, Guowei Liu, Xi Cheng, Jiří
    Friml, Harro Bouwmeester, Enrico Martinoia, and Lorenzo Borghi. “Asymmetric Localizations
    of the ABC Transporter PaPDR1 Trace Paths of Directional Strigolactone Transport.”
    <i>Current Biology</i>. Cell Press, 2015. <a href="https://doi.org/10.1016/j.cub.2015.01.015">https://doi.org/10.1016/j.cub.2015.01.015</a>.
  ieee: J. Sasse <i>et al.</i>, “Asymmetric localizations of the ABC transporter PaPDR1
    trace paths of directional strigolactone transport,” <i>Current Biology</i>, vol.
    25, no. 5. Cell Press, pp. 647–655, 2015.
  ista: Sasse J, Simon S, Gübeli C, Liu G, Cheng X, Friml J, Bouwmeester H, Martinoia
    E, Borghi L. 2015. Asymmetric localizations of the ABC transporter PaPDR1 trace
    paths of directional strigolactone transport. Current Biology. 25(5), 647–655.
  mla: Sasse, Joëlle, et al. “Asymmetric Localizations of the ABC Transporter PaPDR1
    Trace Paths of Directional Strigolactone Transport.” <i>Current Biology</i>, vol.
    25, no. 5, Cell Press, 2015, pp. 647–55, doi:<a href="https://doi.org/10.1016/j.cub.2015.01.015">10.1016/j.cub.2015.01.015</a>.
  short: J. Sasse, S. Simon, C. Gübeli, G. Liu, X. Cheng, J. Friml, H. Bouwmeester,
    E. Martinoia, L. Borghi, Current Biology 25 (2015) 647–655.
date_created: 2018-12-11T11:52:35Z
date_published: 2015-02-12T00:00:00Z
date_updated: 2025-09-23T07:57:02Z
day: '12'
department:
- _id: JiFr
doi: 10.1016/j.cub.2015.01.015
external_id:
  isi:
  - '000350708800029'
intvolume: '        25'
isi: 1
issue: '5'
language:
- iso: eng
month: '02'
oa_version: None
page: 647 - 655
publication: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '5635'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Asymmetric localizations of the ABC transporter PaPDR1 trace paths of directional
  strigolactone transport
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 25
year: '2015'
...
---
_id: '1543'
abstract:
- lang: eng
  text: A plethora of diverse programmed cell death (PCD) processes has been described
    in living organisms. In animals and plants, different forms of PCD play crucial
    roles in development, immunity, and responses to the environment. While the molecular
    control of some animal PCD forms such as apoptosis is known in great detail, we
    still know comparatively little about the regulation of the diverse types of plant
    PCD. In part, this deficiency in molecular understanding is caused by the lack
    of reliable reporters to detect PCD processes. Here, we addressed this issue by
    using a combination of bioinformatics approaches to identify commonly regulated
    genes during diverse plant PCD processes in Arabidopsis (Arabidopsis thaliana).
    Our results indicate that the transcriptional signatures of developmentally controlled
    cell death are largely distinct from the ones associated with environmentally
    induced cell death. Moreover, different cases of developmental PCD share a set
    of cell death-associated genes. Most of these genes are evolutionary conserved
    within the green plant lineage, arguing for an evolutionary conserved core machinery
    of developmental PCD. Based on this information, we established an array of specific
    promoter-reporter lines for developmental PCD in Arabidopsis. These PCD indicators
    represent a powerful resource that can be used in addition to established morphological
    and biochemical methods to detect and analyze PCD processes in vivo and in planta.
article_processing_charge: No
author:
- first_name: Yadira
  full_name: Olvera Carrillo, Yadira
  last_name: Olvera Carrillo
- first_name: Michiel
  full_name: Van Bel, Michiel
  last_name: Van Bel
- first_name: Tom
  full_name: Van Hautegem, Tom
  last_name: Van Hautegem
- first_name: Matyas
  full_name: Fendrych, Matyas
  id: 43905548-F248-11E8-B48F-1D18A9856A87
  last_name: Fendrych
  orcid: 0000-0002-9767-8699
- first_name: Marlies
  full_name: Huysmans, Marlies
  last_name: Huysmans
- first_name: Mária
  full_name: Šimášková, Mária
  last_name: Šimášková
- first_name: Matthias
  full_name: Van Durme, Matthias
  last_name: Van Durme
- first_name: Pierre
  full_name: Buscaill, Pierre
  last_name: Buscaill
- first_name: Susana
  full_name: Rivas, Susana
  last_name: Rivas
- first_name: Núria
  full_name: Coll, Núria
  last_name: Coll
- first_name: Frederik
  full_name: Coppens, Frederik
  last_name: Coppens
- first_name: Steven
  full_name: Maere, Steven
  last_name: Maere
- first_name: Moritz
  full_name: Nowack, Moritz
  last_name: Nowack
citation:
  ama: Olvera Carrillo Y, Van Bel M, Van Hautegem T, et al. A conserved core of programmed
    cell death indicator genes discriminates developmentally and environmentally induced
    programmed cell death in plants. <i>Plant Physiology</i>. 2015;169(4):2684-2699.
    doi:<a href="https://doi.org/10.1104/pp.15.00769">10.1104/pp.15.00769</a>
  apa: Olvera Carrillo, Y., Van Bel, M., Van Hautegem, T., Fendrych, M., Huysmans,
    M., Šimášková, M., … Nowack, M. (2015). A conserved core of programmed cell death
    indicator genes discriminates developmentally and environmentally induced programmed
    cell death in plants. <i>Plant Physiology</i>. American Society of Plant Biologists.
    <a href="https://doi.org/10.1104/pp.15.00769">https://doi.org/10.1104/pp.15.00769</a>
  chicago: Olvera Carrillo, Yadira, Michiel Van Bel, Tom Van Hautegem, Matyas Fendrych,
    Marlies Huysmans, Mária Šimášková, Matthias Van Durme, et al. “A Conserved Core
    of Programmed Cell Death Indicator Genes Discriminates Developmentally and Environmentally
    Induced Programmed Cell Death in Plants.” <i>Plant Physiology</i>. American Society
    of Plant Biologists, 2015. <a href="https://doi.org/10.1104/pp.15.00769">https://doi.org/10.1104/pp.15.00769</a>.
  ieee: Y. Olvera Carrillo <i>et al.</i>, “A conserved core of programmed cell death
    indicator genes discriminates developmentally and environmentally induced programmed
    cell death in plants,” <i>Plant Physiology</i>, vol. 169, no. 4. American Society
    of Plant Biologists, pp. 2684–2699, 2015.
  ista: Olvera Carrillo Y, Van Bel M, Van Hautegem T, Fendrych M, Huysmans M, Šimášková
    M, Van Durme M, Buscaill P, Rivas S, Coll N, Coppens F, Maere S, Nowack M. 2015.
    A conserved core of programmed cell death indicator genes discriminates developmentally
    and environmentally induced programmed cell death in plants. Plant Physiology.
    169(4), 2684–2699.
  mla: Olvera Carrillo, Yadira, et al. “A Conserved Core of Programmed Cell Death
    Indicator Genes Discriminates Developmentally and Environmentally Induced Programmed
    Cell Death in Plants.” <i>Plant Physiology</i>, vol. 169, no. 4, American Society
    of Plant Biologists, 2015, pp. 2684–99, doi:<a href="https://doi.org/10.1104/pp.15.00769">10.1104/pp.15.00769</a>.
  short: Y. Olvera Carrillo, M. Van Bel, T. Van Hautegem, M. Fendrych, M. Huysmans,
    M. Šimášková, M. Van Durme, P. Buscaill, S. Rivas, N. Coll, F. Coppens, S. Maere,
    M. Nowack, Plant Physiology 169 (2015) 2684–2699.
date_created: 2018-12-11T11:52:38Z
date_published: 2015-12-01T00:00:00Z
date_updated: 2025-09-22T14:28:43Z
day: '01'
department:
- _id: JiFr
doi: 10.1104/pp.15.00769
external_id:
  isi:
  - '000368472700025'
intvolume: '       169'
isi: 1
issue: '4'
language:
- iso: eng
month: '12'
oa_version: None
page: 2684 - 2699
publication: Plant Physiology
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '5628'
scopus_import: '1'
status: public
title: A conserved core of programmed cell death indicator genes discriminates developmentally
  and environmentally induced programmed cell death in plants
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 169
year: '2015'
...
---
_id: '1554'
abstract:
- lang: eng
  text: The visualization of hormonal signaling input and output is key to understanding
    how multicellular development is regulated. The plant signaling molecule auxin
    triggers many growth and developmental responses, but current tools lack the sensitivity
    or precision to visualize these. We developed a set of fluorescent reporters that
    allow sensitive and semiquantitative readout of auxin responses at cellular resolution
    in Arabidopsis thaliana. These generic tools are suitable for any transformable
    plant species.
article_processing_charge: No
author:
- first_name: Cheyang
  full_name: Liao, Cheyang
  last_name: Liao
- first_name: Wouter
  full_name: Smet, Wouter
  last_name: Smet
- first_name: Géraldine
  full_name: Brunoud, Géraldine
  last_name: Brunoud
- first_name: Saiko
  full_name: Yoshida, Saiko
  id: 2E46069C-F248-11E8-B48F-1D18A9856A87
  last_name: Yoshida
- first_name: Teva
  full_name: Vernoux, Teva
  last_name: Vernoux
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
citation:
  ama: Liao C, Smet W, Brunoud G, Yoshida S, Vernoux T, Weijers D. Reporters for sensitive
    and quantitative measurement of auxin response. <i>Nature Methods</i>. 2015;12(3):207-210.
    doi:<a href="https://doi.org/10.1038/nmeth.3279">10.1038/nmeth.3279</a>
  apa: Liao, C., Smet, W., Brunoud, G., Yoshida, S., Vernoux, T., &#38; Weijers, D.
    (2015). Reporters for sensitive and quantitative measurement of auxin response.
    <i>Nature Methods</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nmeth.3279">https://doi.org/10.1038/nmeth.3279</a>
  chicago: Liao, Cheyang, Wouter Smet, Géraldine Brunoud, Saiko Yoshida, Teva Vernoux,
    and Dolf Weijers. “Reporters for Sensitive and Quantitative Measurement of Auxin
    Response.” <i>Nature Methods</i>. Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/nmeth.3279">https://doi.org/10.1038/nmeth.3279</a>.
  ieee: C. Liao, W. Smet, G. Brunoud, S. Yoshida, T. Vernoux, and D. Weijers, “Reporters
    for sensitive and quantitative measurement of auxin response,” <i>Nature Methods</i>,
    vol. 12, no. 3. Nature Publishing Group, pp. 207–210, 2015.
  ista: Liao C, Smet W, Brunoud G, Yoshida S, Vernoux T, Weijers D. 2015. Reporters
    for sensitive and quantitative measurement of auxin response. Nature Methods.
    12(3), 207–210.
  mla: Liao, Cheyang, et al. “Reporters for Sensitive and Quantitative Measurement
    of Auxin Response.” <i>Nature Methods</i>, vol. 12, no. 3, Nature Publishing Group,
    2015, pp. 207–10, doi:<a href="https://doi.org/10.1038/nmeth.3279">10.1038/nmeth.3279</a>.
  short: C. Liao, W. Smet, G. Brunoud, S. Yoshida, T. Vernoux, D. Weijers, Nature
    Methods 12 (2015) 207–210.
date_created: 2018-12-11T11:52:41Z
date_published: 2015-02-26T00:00:00Z
date_updated: 2025-09-23T10:34:32Z
day: '26'
department:
- _id: JiFr
doi: 10.1038/nmeth.3279
external_id:
  isi:
  - '000350670300017'
  pmid:
  - '25643149'
intvolume: '        12'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344836/
month: '02'
oa: 1
oa_version: Submitted Version
page: 207 - 210
pmid: 1
publication: Nature Methods
publication_status: published
publisher: Nature Publishing Group
publist_id: '5617'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Reporters for sensitive and quantitative measurement of auxin response
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 12
year: '2015'
...
---
_id: '1556'
abstract:
- lang: eng
  text: The elongator complex subunit 2 (ELP2) protein, one subunit of an evolutionarily
    conserved histone acetyltransferase complex, has been shown to participate in
    leaf patterning, plant immune and abiotic stress responses in Arabidopsis thaliana.
    Here, its role in root development was explored. Compared to the wild type, the
    elp2 mutant exhibited an accelerated differentiation of its root stem cells and
    cell division was more active in its quiescent centre (QC). The key transcription
    factors responsible for maintaining root stem cell and QC identity, such as AP2
    transcription factors PLT1 (PLETHORA1) and PLT2 (PLETHORA2), GRAS transcription
    factors such as SCR (SCARECROW) and SHR (SHORT ROOT) and WUSCHEL-RELATED HOMEOBOX5
    transcription factor WOX5, were all strongly down-regulated in the mutant. On
    the other hand, expression of the G2/M transition activator CYCB1 was substantially
    induced in elp2. The auxin efflux transporters PIN1 and PIN2 showed decreased
    protein levels and PIN1 also displayed mild polarity alterations in elp2, which
    resulted in a reduced auxin content in the root tip. Either the acetylation or
    methylation level of each of these genes differed between the mutant and the wild
    type, suggesting that the ELP2 regulation of root development involves the epigenetic
    modification of a range of transcription factors and other developmental regulators.
article_processing_charge: No
author:
- first_name: Yuebin
  full_name: Jia, Yuebin
  last_name: Jia
- first_name: Huiyu
  full_name: Tian, Huiyu
  last_name: Tian
- first_name: Hongjiang
  full_name: Li, Hongjiang
  id: 33CA54A6-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0001-5039-9660
- first_name: Qianqian
  full_name: Yu, Qianqian
  last_name: Yu
- first_name: Lei
  full_name: Wang, Lei
  last_name: Wang
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Zhaojun
  full_name: Ding, Zhaojun
  last_name: Ding
citation:
  ama: Jia Y, Tian H, Li H, et al. The Arabidopsis thaliana elongator complex subunit
    2 epigenetically affects root development. <i>Journal of Experimental Botany</i>.
    2015;66(15):4631-4642. doi:<a href="https://doi.org/10.1093/jxb/erv230">10.1093/jxb/erv230</a>
  apa: Jia, Y., Tian, H., Li, H., Yu, Q., Wang, L., Friml, J., &#38; Ding, Z. (2015).
    The Arabidopsis thaliana elongator complex subunit 2 epigenetically affects root
    development. <i>Journal of Experimental Botany</i>. Oxford University Press. <a
    href="https://doi.org/10.1093/jxb/erv230">https://doi.org/10.1093/jxb/erv230</a>
  chicago: Jia, Yuebin, Huiyu Tian, Hongjiang Li, Qianqian Yu, Lei Wang, Jiří Friml,
    and Zhaojun Ding. “The Arabidopsis Thaliana Elongator Complex Subunit 2 Epigenetically
    Affects Root Development.” <i>Journal of Experimental Botany</i>. Oxford University
    Press, 2015. <a href="https://doi.org/10.1093/jxb/erv230">https://doi.org/10.1093/jxb/erv230</a>.
  ieee: Y. Jia <i>et al.</i>, “The Arabidopsis thaliana elongator complex subunit
    2 epigenetically affects root development,” <i>Journal of Experimental Botany</i>,
    vol. 66, no. 15. Oxford University Press, pp. 4631–4642, 2015.
  ista: Jia Y, Tian H, Li H, Yu Q, Wang L, Friml J, Ding Z. 2015. The Arabidopsis
    thaliana elongator complex subunit 2 epigenetically affects root development.
    Journal of Experimental Botany. 66(15), 4631–4642.
  mla: Jia, Yuebin, et al. “The Arabidopsis Thaliana Elongator Complex Subunit 2 Epigenetically
    Affects Root Development.” <i>Journal of Experimental Botany</i>, vol. 66, no.
    15, Oxford University Press, 2015, pp. 4631–42, doi:<a href="https://doi.org/10.1093/jxb/erv230">10.1093/jxb/erv230</a>.
  short: Y. Jia, H. Tian, H. Li, Q. Yu, L. Wang, J. Friml, Z. Ding, Journal of Experimental
    Botany 66 (2015) 4631–4642.
date_created: 2018-12-11T11:52:42Z
date_published: 2015-08-01T00:00:00Z
date_updated: 2025-09-23T13:42:27Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1093/jxb/erv230
external_id:
  isi:
  - '000359687400017'
file:
- access_level: open_access
  checksum: 257919be0ce3d306185d3891ad7acf39
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:02Z
  date_updated: 2020-07-14T12:45:02Z
  file_id: '5051'
  file_name: IST-2016-480-v1+1_J._Exp._Bot.-2015-Jia-4631-42.pdf
  file_size: 7753043
  relation: main_file
file_date_updated: 2020-07-14T12:45:02Z
has_accepted_license: '1'
intvolume: '        66'
isi: 1
issue: '15'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 4631 - 4642
publication: Journal of Experimental Botany
publication_status: published
publisher: Oxford University Press
publist_id: '5615'
pubrep_id: '480'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Arabidopsis thaliana elongator complex subunit 2 epigenetically affects
  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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 66
year: '2015'
...
---
_id: '1558'
abstract:
- lang: eng
  text: CyclophilinAis a conserved peptidyl-prolyl cis-trans isomerase (PPIase) best
    known as the cellular receptor of the immunosuppressant cyclosporine A. Despite
    significant effort, evidence of developmental functions of cyclophilin A in non-plant
    systems has remained obscure. Mutations in a tomato (Solanum lycopersicum) cyclophilin
    A ortholog, DIAGEOTROPICA (DGT), have been shown to abolish the organogenesis
    of lateral roots; however, a mechanistic explanation of the phenotype is lacking.
    Here, we show that the dgt mutant lacks auxin maxima relevant to priming and specification
    of lateral root founder cells. DGT is expressed in shoot and root, and localizes
    to both the nucleus and cytoplasm during lateral root organogenesis. Mutation
    of ENTIRE/ IAA9, a member of the auxin-responsive Aux/IAA protein family of transcriptional
    repressors, partially restores the inability of dgt to initiate lateral root primordia
    but not the primordia outgrowth. By comparison, grafting of a wild-type scion
    restores the process of lateral root formation, consistent with participation
    of a mobile signal. Antibodies do not detect movement of the DGT protein into
    the dgt rootstock; however, experiments with radiolabeled auxin and an auxin-specific
    microelectrode demonstrate abnormal auxin fluxes. Functional studies of DGT in
    heterologous yeast and tobacco-leaf auxin-transport systems demonstrate that DGT
    negatively regulates PIN-FORMED (PIN) auxin efflux transporters by affecting their
    plasma membrane localization. Studies in tomato support complex effects of the
    dgt mutation on PIN expression level, expression domain and plasma membrane localization.
    Our data demonstrate that DGT regulates auxin transport in lateral root formation.
article_processing_charge: No
author:
- first_name: Maria
  full_name: Ivanchenko, Maria
  last_name: Ivanchenko
- first_name: Jinsheng
  full_name: Zhu, Jinsheng
  last_name: Zhu
- first_name: Bangjun
  full_name: Wang, Bangjun
  last_name: Wang
- first_name: Eva
  full_name: Medvecka, Eva
  id: 298814E2-F248-11E8-B48F-1D18A9856A87
  last_name: Medvecka
- first_name: Yunlong
  full_name: Du, Yunlong
  last_name: Du
- first_name: Elisa
  full_name: Azzarello, Elisa
  last_name: Azzarello
- first_name: Stefano
  full_name: Mancuso, Stefano
  last_name: Mancuso
- first_name: Molly
  full_name: Megraw, Molly
  last_name: Megraw
- first_name: Sergei
  full_name: Filichkin, Sergei
  last_name: Filichkin
- first_name: Joseph
  full_name: Dubrovsky, Joseph
  last_name: Dubrovsky
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Markus
  full_name: Geisler, Markus
  last_name: Geisler
citation:
  ama: Ivanchenko M, Zhu J, Wang B, et al. The cyclophilin a DIAGEOTROPICA gene affects
    auxin transport in both root and shoot to control lateral root formation. <i>Development</i>.
    2015;142(4):712-721. doi:<a href="https://doi.org/10.1242/dev.113225">10.1242/dev.113225</a>
  apa: Ivanchenko, M., Zhu, J., Wang, B., Medvecka, E., Du, Y., Azzarello, E., … Geisler,
    M. (2015). The cyclophilin a DIAGEOTROPICA gene affects auxin transport in both
    root and shoot to control lateral root formation. <i>Development</i>. Company
    of Biologists. <a href="https://doi.org/10.1242/dev.113225">https://doi.org/10.1242/dev.113225</a>
  chicago: Ivanchenko, Maria, Jinsheng Zhu, Bangjun Wang, Eva Medvecka, Yunlong Du,
    Elisa Azzarello, Stefano Mancuso, et al. “The Cyclophilin a DIAGEOTROPICA Gene
    Affects Auxin Transport in Both Root and Shoot to Control Lateral Root Formation.”
    <i>Development</i>. Company of Biologists, 2015. <a href="https://doi.org/10.1242/dev.113225">https://doi.org/10.1242/dev.113225</a>.
  ieee: M. Ivanchenko <i>et al.</i>, “The cyclophilin a DIAGEOTROPICA gene affects
    auxin transport in both root and shoot to control lateral root formation,” <i>Development</i>,
    vol. 142, no. 4. Company of Biologists, pp. 712–721, 2015.
  ista: Ivanchenko M, Zhu J, Wang B, Medvecka E, Du Y, Azzarello E, Mancuso S, Megraw
    M, Filichkin S, Dubrovsky J, Friml J, Geisler M. 2015. The cyclophilin a DIAGEOTROPICA
    gene affects auxin transport in both root and shoot to control lateral root formation.
    Development. 142(4), 712–721.
  mla: Ivanchenko, Maria, et al. “The Cyclophilin a DIAGEOTROPICA Gene Affects Auxin
    Transport in Both Root and Shoot to Control Lateral Root Formation.” <i>Development</i>,
    vol. 142, no. 4, Company of Biologists, 2015, pp. 712–21, doi:<a href="https://doi.org/10.1242/dev.113225">10.1242/dev.113225</a>.
  short: M. Ivanchenko, J. Zhu, B. Wang, E. Medvecka, Y. Du, E. Azzarello, S. Mancuso,
    M. Megraw, S. Filichkin, J. Dubrovsky, J. Friml, M. Geisler, Development 142 (2015)
    712–721.
date_created: 2018-12-11T11:52:42Z
date_published: 2015-02-15T00:00:00Z
date_updated: 2025-09-23T13:49:06Z
day: '15'
department:
- _id: JiFr
doi: 10.1242/dev.113225
external_id:
  isi:
  - '000351697100012'
intvolume: '       142'
isi: 1
issue: '4'
language:
- iso: eng
month: '02'
oa_version: None
page: 712 - 721
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '5613'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The cyclophilin a DIAGEOTROPICA gene affects auxin transport in both root and
  shoot to control lateral root formation
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 142
year: '2015'
...
---
_id: '1562'
abstract:
- lang: eng
  text: The plant hormone auxin is a key regulator of plant growth and development.
    Auxin levels are sensed and interpreted by distinct receptor systems that activate
    a broad range of cellular responses. The Auxin-Binding Protein1 (ABP1) that has
    been identified based on its ability to bind auxin with high affinity is a prime
    candidate for the extracellular receptor responsible for mediating a range of
    auxin effects, in particular, the fast non-transcriptional ones. Contradictory
    genetic studies suggested prominent or no importance of ABP1 in many developmental
    processes. However, how crucial the role of auxin binding to ABP1 is for its functions
    has not been addressed. Here, we show that the auxin-binding pocket of ABP1 is
    essential for its gain-of-function cellular and developmental roles. In total,
    16 different abp1 mutants were prepared that possessed substitutions in the metal
    core or in the hydrophobic amino acids of the auxin-binding pocket as well as
    neutral mutations. Their analysis revealed that an intact auxin-binding pocket
    is a prerequisite for ABP1 to activate downstream components of the ABP1 signalling
    pathway, such as Rho of Plants (ROPs) and to mediate the clathrin association
    with membranes for endocytosis regulation. In planta analyses demonstrated the
    importance of the auxin binding pocket for all known ABP1-mediated postembryonic
    developmental processes, including morphology of leaf epidermal cells, root growth
    and root meristem activity, and vascular tissue differentiation. Taken together,
    these findings suggest that auxin binding to ABP1 is central to its function,
    supporting the role of ABP1 as auxin receptor.
acknowledgement: This work was supported by ERC Independent Research grant (ERC-2011-StG-
  20101109-PSDP to JF); the European Social Fund and the state budget of the Czech
  Republic [the project ‘Employment of Newly Graduated Doctors of Science for Scientific
  Excellence’ (CZ.1.07/2.3.00/30.0009) to TN]; the Czech Science Foundation (GACR)
  [project 13-40637S to JF].
article_processing_charge: No
article_type: original
author:
- first_name: Peter
  full_name: Grones, Peter
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- first_name: Xu
  full_name: Chen, Xu
  id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87
  last_name: Chen
- first_name: Sibu
  full_name: Simon, Sibu
  id: 4542EF9A-F248-11E8-B48F-1D18A9856A87
  last_name: Simon
  orcid: 0000-0002-1998-6741
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Riet
  full_name: De Rycke, Riet
  last_name: De Rycke
- first_name: Tomasz
  full_name: Nodzyński, Tomasz
  last_name: Nodzyński
- first_name: Eva
  full_name: Zažímalová, Eva
  last_name: Zažímalová
- 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, Chen X, Simon S, et al. Auxin-binding pocket of ABP1 is crucial for
    its gain-of-function cellular and developmental roles. <i>Journal of Experimental
    Botany</i>. 2015;66(16):5055-5065. doi:<a href="https://doi.org/10.1093/jxb/erv177">10.1093/jxb/erv177</a>
  apa: Grones, P., Chen, X., Simon, S., Kaufmann, W., De Rycke, R., Nodzyński, T.,
    … Friml, J. (2015). Auxin-binding pocket of ABP1 is crucial for its gain-of-function
    cellular and developmental roles. <i>Journal of Experimental Botany</i>. Oxford
    University Press. <a href="https://doi.org/10.1093/jxb/erv177">https://doi.org/10.1093/jxb/erv177</a>
  chicago: Grones, Peter, Xu Chen, Sibu Simon, Walter Kaufmann, Riet De Rycke, Tomasz
    Nodzyński, Eva Zažímalová, and Jiří Friml. “Auxin-Binding Pocket of ABP1 Is Crucial
    for Its Gain-of-Function Cellular and Developmental Roles.” <i>Journal of Experimental
    Botany</i>. Oxford University Press, 2015. <a href="https://doi.org/10.1093/jxb/erv177">https://doi.org/10.1093/jxb/erv177</a>.
  ieee: P. Grones <i>et al.</i>, “Auxin-binding pocket of ABP1 is crucial for its
    gain-of-function cellular and developmental roles,” <i>Journal of Experimental
    Botany</i>, vol. 66, no. 16. Oxford University Press, pp. 5055–5065, 2015.
  ista: Grones P, Chen X, Simon S, Kaufmann W, De Rycke R, Nodzyński T, Zažímalová
    E, Friml J. 2015. Auxin-binding pocket of ABP1 is crucial for its gain-of-function
    cellular and developmental roles. Journal of Experimental Botany. 66(16), 5055–5065.
  mla: Grones, Peter, et al. “Auxin-Binding Pocket of ABP1 Is Crucial for Its Gain-of-Function
    Cellular and Developmental Roles.” <i>Journal of Experimental Botany</i>, vol.
    66, no. 16, Oxford University Press, 2015, pp. 5055–65, doi:<a href="https://doi.org/10.1093/jxb/erv177">10.1093/jxb/erv177</a>.
  short: P. Grones, X. Chen, S. Simon, W. Kaufmann, R. De Rycke, T. Nodzyński, E.
    Zažímalová, J. Friml, Journal of Experimental Botany 66 (2015) 5055–5065.
corr_author: '1'
date_created: 2018-12-11T11:52:44Z
date_published: 2015-08-01T00:00:00Z
date_updated: 2025-09-23T07:59:07Z
day: '01'
department:
- _id: JiFr
- _id: EM-Fac
doi: 10.1093/jxb/erv177
ec_funded: 1
external_id:
  isi:
  - '000359688300017'
intvolume: '        66'
isi: 1
issue: '16'
language:
- iso: eng
month: '08'
oa_version: None
page: 5055 - 5065
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_status: published
publisher: Oxford University Press
publist_id: '5609'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Auxin-binding pocket of ABP1 is crucial for its gain-of-function cellular and
  developmental roles
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 66
year: '2015'
...
---
_id: '1569'
abstract:
- lang: eng
  text: Spatial regulation of the plant hormone indole-3-acetic acid (IAA, or auxin)
    is essential for plant development. Auxin gradient establishment is mediated by
    polarly localized auxin transporters, including PIN-FORMED (PIN) proteins. Their
    localization and abundance at the plasma membrane are tightly regulated by endomembrane
    machinery, especially the endocytic and recycling pathways mediated by the ADP
    ribosylation factor guanine nucleotide exchange factor (ARF-GEF) GNOM. We assessed
    the role of the early secretory pathway in establishing PIN1 polarity in Arabidopsis
    thaliana by pharmacological and genetic approaches. We identified the compound
    endosidin 8 (ES8), which selectively interferes with PIN1 basal polarity without
    altering the polarity of apical proteins. ES8 alters the auxin distribution pattern
    in the root and induces a strong developmental phenotype, including reduced root
    length. The ARF-GEF- defective mutants gnom-like 1 ( gnl1-1) and gnom ( van7)
    are significantly resistant to ES8. The compound does not affect recycling or
    vacuolar trafficking of PIN1 but leads to its intracellular accumulation, resulting
    in loss of PIN1 basal polarity at the plasma membrane. Our data confirm a role
    for GNOM in endoplasmic reticulum (ER) - Golgi trafficking and reveal that a GNL1/GNOM-mediated
    early secretory pathway selectively regulates PIN1 basal polarity establishment
    in a manner essential for normal plant development.
acknowledgement: 'This work was supported by Vetenskapsrådet and Vinnova (Verket för
  Innovationssystemet) (S.M.D., T.V., M.Ł., and S.R.), Knut och Alice Wallenbergs
  Stiftelse (S.M.D., A.R., and C.V.), Kempestiftelserna (A.H. and Q.M.), Carl Tryggers
  Stiftelse för Vetenskaplig Forskning (Q.M.), European Research Council Grant ERC-2011-StG-20101109-PSDP
  (to J.F.), US Department of Energy Grant DE-FG02-02ER15295 (to N.V.R.), and National
  Science Foundation Grant MCB-0817916 (to N.V.R. and G.R.H.). '
article_processing_charge: No
author:
- first_name: Siamsa
  full_name: Doyle, Siamsa
  last_name: Doyle
- first_name: Ash
  full_name: Haegera, Ash
  last_name: Haegera
- first_name: Thomas
  full_name: Vain, Thomas
  last_name: Vain
- first_name: Adeline
  full_name: Rigala, Adeline
  last_name: Rigala
- first_name: Corrado
  full_name: Viotti, Corrado
  last_name: Viotti
- first_name: Małgorzata
  full_name: Łangowskaa, Małgorzata
  last_name: Łangowskaa
- first_name: Qian
  full_name: Maa, Qian
  last_name: Maa
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Natasha
  full_name: Raikhel, Natasha
  last_name: Raikhel
- first_name: Glenn
  full_name: Hickse, Glenn
  last_name: Hickse
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
citation:
  ama: Doyle S, Haegera A, Vain T, et al. An early secretory pathway mediated by gnom-like
    1 and gnom is essential for basal polarity establishment in Arabidopsis thaliana.
    <i>PNAS</i>. 2015;112(7):E806-E815. doi:<a href="https://doi.org/10.1073/pnas.1424856112">10.1073/pnas.1424856112</a>
  apa: Doyle, S., Haegera, A., Vain, T., Rigala, A., Viotti, C., Łangowskaa, M., …
    Robert, S. (2015). An early secretory pathway mediated by gnom-like 1 and gnom
    is essential for basal polarity establishment in Arabidopsis thaliana. <i>PNAS</i>.
    National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1424856112">https://doi.org/10.1073/pnas.1424856112</a>
  chicago: Doyle, Siamsa, Ash Haegera, Thomas Vain, Adeline Rigala, Corrado Viotti,
    Małgorzata Łangowskaa, Qian Maa, et al. “An Early Secretory Pathway Mediated by
    Gnom-like 1 and Gnom Is Essential for Basal Polarity Establishment in Arabidopsis
    Thaliana.” <i>PNAS</i>. National Academy of Sciences, 2015. <a href="https://doi.org/10.1073/pnas.1424856112">https://doi.org/10.1073/pnas.1424856112</a>.
  ieee: S. Doyle <i>et al.</i>, “An early secretory pathway mediated by gnom-like
    1 and gnom is essential for basal polarity establishment in Arabidopsis thaliana,”
    <i>PNAS</i>, vol. 112, no. 7. National Academy of Sciences, pp. E806–E815, 2015.
  ista: Doyle S, Haegera A, Vain T, Rigala A, Viotti C, Łangowskaa M, Maa Q, Friml
    J, Raikhel N, Hickse G, Robert S. 2015. An early secretory pathway mediated by
    gnom-like 1 and gnom is essential for basal polarity establishment in Arabidopsis
    thaliana. PNAS. 112(7), E806–E815.
  mla: Doyle, Siamsa, et al. “An Early Secretory Pathway Mediated by Gnom-like 1 and
    Gnom Is Essential for Basal Polarity Establishment in Arabidopsis Thaliana.” <i>PNAS</i>,
    vol. 112, no. 7, National Academy of Sciences, 2015, pp. E806–15, doi:<a href="https://doi.org/10.1073/pnas.1424856112">10.1073/pnas.1424856112</a>.
  short: S. Doyle, A. Haegera, T. Vain, A. Rigala, C. Viotti, M. Łangowskaa, Q. Maa,
    J. Friml, N. Raikhel, G. Hickse, S. Robert, PNAS 112 (2015) E806–E815.
date_created: 2018-12-11T11:52:46Z
date_published: 2015-02-17T00:00:00Z
date_updated: 2026-06-18T17:48:36Z
day: '17'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1073/pnas.1424856112
ec_funded: 1
external_id:
  isi:
  - '000349446000025'
intvolume: '       112'
isi: 1
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4343110/
month: '02'
oa: 1
oa_version: Published Version
page: E806 - E815
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: '5602'
quality_controlled: '1'
scopus_import: '1'
status: public
title: An early secretory pathway mediated by gnom-like 1 and gnom is essential for
  basal polarity establishment in Arabidopsis thaliana
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 112
year: '2015'
...
---
_id: '1574'
abstract:
- lang: eng
  text: Multiple plant developmental processes, such as lateral root development,
    depend on auxin distribution patterns that are in part generated by the PIN-formed
    family of auxin-efflux transporters. Here we propose that AUXIN RESPONSE FACTOR7
    (ARF7) and the ARF7-regulated FOUR LIPS/MYB124 (FLP) transcription factors jointly
    form a coherent feed-forward motif that mediates the auxin-responsive PIN3 transcription
    in planta to steer the early steps of lateral root formation. This regulatory
    mechanism might endow the PIN3 circuitry with a temporal 'memory' of auxin stimuli,
    potentially maintaining and enhancing the robustness of the auxin flux directionality
    during lateral root development. The cooperative action between canonical auxin
    signalling and other transcription factors might constitute a general mechanism
    by which transcriptional auxin-sensitivity can be regulated at a tissue-specific
    level.
acknowledgement: 'of the European Research Council (project ERC-2011-StG-20101109-PSDP)
  (to J.F.), a FEBS long-term fellowship (to P.M.) '
article_number: '8821'
article_processing_charge: No
author:
- first_name: Qian
  full_name: Chen, Qian
  last_name: Chen
- first_name: Yang
  full_name: Liu, Yang
  last_name: Liu
- first_name: Steven
  full_name: Maere, Steven
  last_name: Maere
- first_name: Eunkyoung
  full_name: Lee, Eunkyoung
  last_name: Lee
- first_name: Gert
  full_name: Van Isterdael, Gert
  last_name: Van Isterdael
- first_name: Zidian
  full_name: Xie, Zidian
  last_name: Xie
- first_name: Wei
  full_name: Xuan, Wei
  last_name: Xuan
- first_name: Jessica
  full_name: Lucas, Jessica
  last_name: Lucas
- first_name: Valya
  full_name: Vassileva, Valya
  last_name: Vassileva
- first_name: Saeko
  full_name: Kitakura, Saeko
  last_name: Kitakura
- first_name: Peter
  full_name: Marhavy, Peter
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- 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: Niko
  full_name: Geldner, Niko
  last_name: Geldner
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Jie
  full_name: Le, Jie
  last_name: Le
- first_name: Hidehiro
  full_name: Fukaki, Hidehiro
  last_name: Fukaki
- first_name: Erich
  full_name: Grotewold, Erich
  last_name: Grotewold
- first_name: Chuanyou
  full_name: Li, Chuanyou
  last_name: Li
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Fred
  full_name: Sack, Fred
  last_name: Sack
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
citation:
  ama: Chen Q, Liu Y, Maere S, et al. A coherent transcriptional feed-forward motif
    model for mediating auxin-sensitive PIN3 expression during lateral root development.
    <i>Nature Communications</i>. 2015;6. doi:<a href="https://doi.org/10.1038/ncomms9821">10.1038/ncomms9821</a>
  apa: Chen, Q., Liu, Y., Maere, S., Lee, E., Van Isterdael, G., Xie, Z., … Vanneste,
    S. (2015). A coherent transcriptional feed-forward motif model for mediating auxin-sensitive
    PIN3 expression during lateral root development. <i>Nature Communications</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/ncomms9821">https://doi.org/10.1038/ncomms9821</a>
  chicago: Chen, Qian, Yang Liu, Steven Maere, Eunkyoung Lee, Gert Van Isterdael,
    Zidian Xie, Wei Xuan, et al. “A Coherent Transcriptional Feed-Forward Motif Model
    for Mediating Auxin-Sensitive PIN3 Expression during Lateral Root Development.”
    <i>Nature Communications</i>. Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/ncomms9821">https://doi.org/10.1038/ncomms9821</a>.
  ieee: Q. Chen <i>et al.</i>, “A coherent transcriptional feed-forward motif model
    for mediating auxin-sensitive PIN3 expression during lateral root development,”
    <i>Nature Communications</i>, vol. 6. Nature Publishing Group, 2015.
  ista: Chen Q, Liu Y, Maere S, Lee E, Van Isterdael G, Xie Z, Xuan W, Lucas J, Vassileva
    V, Kitakura S, Marhavý P, Wabnik KT, Geldner N, Benková E, Le J, Fukaki H, Grotewold
    E, Li C, Friml J, Sack F, Beeckman T, Vanneste S. 2015. A coherent transcriptional
    feed-forward motif model for mediating auxin-sensitive PIN3 expression during
    lateral root development. Nature Communications. 6, 8821.
  mla: Chen, Qian, et al. “A Coherent Transcriptional Feed-Forward Motif Model for
    Mediating Auxin-Sensitive PIN3 Expression during Lateral Root Development.” <i>Nature
    Communications</i>, vol. 6, 8821, Nature Publishing Group, 2015, doi:<a href="https://doi.org/10.1038/ncomms9821">10.1038/ncomms9821</a>.
  short: Q. Chen, Y. Liu, S. Maere, E. Lee, G. Van Isterdael, Z. Xie, W. Xuan, J.
    Lucas, V. Vassileva, S. Kitakura, P. Marhavý, K.T. Wabnik, N. Geldner, E. Benková,
    J. Le, H. Fukaki, E. Grotewold, C. Li, J. Friml, F. Sack, T. Beeckman, S. Vanneste,
    Nature Communications 6 (2015).
date_created: 2018-12-11T11:52:48Z
date_published: 2015-11-18T00:00:00Z
date_updated: 2025-09-22T14:28:09Z
day: '18'
ddc:
- '580'
department:
- _id: EvBe
- _id: JiFr
doi: 10.1038/ncomms9821
external_id:
  isi:
  - '000366295500007'
file:
- access_level: open_access
  checksum: 8ff5c108899b548806e1cb7a302fe76d
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:32Z
  date_updated: 2020-07-14T12:45:02Z
  file_id: '5085'
  file_name: IST-2016-477-v1+1_ncomms9821.pdf
  file_size: 1701815
  relation: main_file
file_date_updated: 2020-07-14T12:45:02Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Nature Communications
publication_status: published
publisher: Nature Publishing Group
publist_id: '5597'
pubrep_id: '477'
quality_controlled: '1'
scopus_import: '1'
status: public
title: A coherent transcriptional feed-forward motif model for mediating auxin-sensitive
  PIN3 expression during lateral 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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 6
year: '2015'
...
---
_id: '1591'
abstract:
- lang: eng
  text: Auxin participates in a multitude of developmental processes, as well as responses
    to environmental cues. Compared with other plant hormones, auxin exhibits a unique
    property, as it undergoes directional, cell-to-cell transport facilitated by plasma
    membrane-localized transport proteins. Among them, a prominent role has been ascribed
    to the PIN family of auxin efflux facilitators. PIN proteins direct polar auxin
    transport on account of their asymmetric subcellular localizations. In this review,
    we provide an overview of the multiple developmental roles of PIN proteins, including
    the atypical endoplasmic reticulum-localized members of the family, and look at
    the family from an evolutionary perspective. Next, we cover the cell biological
    and molecular aspects of PIN function, in particular the establishment of their
    polar subcellular localization. Hormonal and environmental inputs into the regulation
    of PIN action are summarized as well.
article_processing_charge: No
author:
- first_name: Maciek
  full_name: Adamowski, Maciek
  id: 45F536D2-F248-11E8-B48F-1D18A9856A87
  last_name: Adamowski
  orcid: 0000-0001-6463-5257
- 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, Friml J. PIN-dependent auxin transport: Action, regulation, and
    evolution. <i>Plant Cell</i>. 2015;27(1):20-32. doi:<a href="https://doi.org/10.1105/tpc.114.134874">10.1105/tpc.114.134874</a>'
  apa: 'Adamowski, M., &#38; Friml, J. (2015). PIN-dependent auxin transport: Action,
    regulation, and evolution. <i>Plant Cell</i>. American Society of Plant Biologists.
    <a href="https://doi.org/10.1105/tpc.114.134874">https://doi.org/10.1105/tpc.114.134874</a>'
  chicago: 'Adamowski, Maciek, and Jiří Friml. “PIN-Dependent Auxin Transport: Action,
    Regulation, and Evolution.” <i>Plant Cell</i>. American Society of Plant Biologists,
    2015. <a href="https://doi.org/10.1105/tpc.114.134874">https://doi.org/10.1105/tpc.114.134874</a>.'
  ieee: 'M. Adamowski and J. Friml, “PIN-dependent auxin transport: Action, regulation,
    and evolution,” <i>Plant Cell</i>, vol. 27, no. 1. American Society of Plant Biologists,
    pp. 20–32, 2015.'
  ista: 'Adamowski M, Friml J. 2015. PIN-dependent auxin transport: Action, regulation,
    and evolution. Plant Cell. 27(1), 20–32.'
  mla: 'Adamowski, Maciek, and Jiří Friml. “PIN-Dependent Auxin Transport: Action,
    Regulation, and Evolution.” <i>Plant Cell</i>, vol. 27, no. 1, American Society
    of Plant Biologists, 2015, pp. 20–32, doi:<a href="https://doi.org/10.1105/tpc.114.134874">10.1105/tpc.114.134874</a>.'
  short: M. Adamowski, J. Friml, Plant Cell 27 (2015) 20–32.
corr_author: '1'
date_created: 2018-12-11T11:52:54Z
date_published: 2015-01-20T00:00:00Z
date_updated: 2026-04-08T14:20:44Z
day: '20'
department:
- _id: JiFr
doi: 10.1105/tpc.114.134874
external_id:
  isi:
  - '000350764700007'
  pmid:
  - '25604445'
intvolume: '        27'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330589/
month: '01'
oa: 1
oa_version: Submitted Version
page: 20 - 32
pmid: 1
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '5580'
quality_controlled: '1'
related_material:
  record:
  - id: '938'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'PIN-dependent auxin transport: Action, regulation, and evolution'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 27
year: '2015'
...
---
_id: '1640'
abstract:
- lang: eng
  text: Auxin and cytokinin are key endogenous regulators of plant development. Although
    cytokinin-mediated modulation of auxin distribution is a developmentally crucial
    hormonal interaction, its molecular basis is largely unknown. Here we show a direct
    regulatory link between cytokinin signalling and the auxin transport machinery
    uncovering a mechanistic framework for cytokinin-auxin cross-talk. We show that
    the CYTOKININ RESPONSE FACTORS (CRFs), transcription factors downstream of cytokinin
    perception, transcriptionally control genes encoding PIN-FORMED (PIN) auxin transporters
    at a specific PIN CYTOKININ RESPONSE ELEMENT (PCRE) domain. Removal of this cis-regulatory
    element effectively uncouples PIN transcription from the CRF-mediated cytokinin
    regulation and attenuates plant cytokinin sensitivity. We propose that CRFs represent
    a missing cross-talk component that fine-tunes auxin transport capacity downstream
    of cytokinin signalling to control plant development.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: This work was supported by the European Research Council Starting
  Independent Research grant (ERC-2007-Stg-207362-HCPO to E.B., M.S., C.C.), by the
  Ghent University Multidisciplinary Research Partnership ‘Biotechnology for a Sustainable
  Economy’ no.01MRB510W, by the Research Foundation—Flanders (grant 3G033711 to J.-A.O.),
  by the Austrian Science Fund (FWF01_I1774S) to K.Ö.,E.B., and by the Interuniversity
  Attraction Poles Programme (IUAP P7/29 ‘MARS’) initiated by the Belgian Science
  Policy Office. I.D.C. and S.V. are post-doctoral fellows of the Research Foundation—Flanders
  (FWO). This research was supported by the Scientific Service Units (SSU) of IST-Austria
  through resources provided by the Bioimaging Facility (BIF), the Life Science Facility
  (LSF).
article_number: '8717'
article_processing_charge: No
author:
- first_name: Mária
  full_name: Šimášková, Mária
  last_name: Šimášková
- first_name: José
  full_name: O'Brien, José
  last_name: O'Brien
- first_name: Mamoona
  full_name: Khan-Djamei, Mamoona
  id: 391B5BBC-F248-11E8-B48F-1D18A9856A87
  last_name: Khan-Djamei
- first_name: Giel
  full_name: Van Noorden, Giel
  last_name: Van Noorden
- first_name: Krisztina
  full_name: Ötvös, Krisztina
  id: 29B901B0-F248-11E8-B48F-1D18A9856A87
  last_name: Ötvös
  orcid: 0000-0002-5503-4983
- first_name: Anne
  full_name: Vieten, Anne
  last_name: Vieten
- first_name: Inge
  full_name: De Clercq, Inge
  last_name: De Clercq
- first_name: Johanna
  full_name: Van Haperen, Johanna
  last_name: Van Haperen
- first_name: Candela
  full_name: Cuesta, Candela
  id: 33A3C818-F248-11E8-B48F-1D18A9856A87
  last_name: Cuesta
  orcid: 0000-0003-1923-2410
- first_name: Klára
  full_name: Hoyerová, Klára
  last_name: Hoyerová
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Peter
  full_name: Marhavy, Peter
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- 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: Frank
  full_name: Van Breusegem, Frank
  last_name: Van Breusegem
- first_name: Moritz
  full_name: Nowack, Moritz
  last_name: Nowack
- first_name: Angus
  full_name: Murphy, Angus
  last_name: Murphy
- first_name: Jiřĺ
  full_name: Friml, Jiřĺ
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Šimášková M, O’Brien J, Khan-Djamei M, et al. Cytokinin response factors regulate
    PIN-FORMED auxin transporters. <i>Nature Communications</i>. 2015;6. doi:<a href="https://doi.org/10.1038/ncomms9717">10.1038/ncomms9717</a>
  apa: Šimášková, M., O’Brien, J., Khan-Djamei, M., Van Noorden, G., Ötvös, K., Vieten,
    A., … Benková, E. (2015). Cytokinin response factors regulate PIN-FORMED auxin
    transporters. <i>Nature Communications</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/ncomms9717">https://doi.org/10.1038/ncomms9717</a>
  chicago: Šimášková, Mária, José O’Brien, Mamoona Khan-Djamei, Giel Van Noorden,
    Krisztina Ötvös, Anne Vieten, Inge De Clercq, et al. “Cytokinin Response Factors
    Regulate PIN-FORMED Auxin Transporters.” <i>Nature Communications</i>. Nature
    Publishing Group, 2015. <a href="https://doi.org/10.1038/ncomms9717">https://doi.org/10.1038/ncomms9717</a>.
  ieee: M. Šimášková <i>et al.</i>, “Cytokinin response factors regulate PIN-FORMED
    auxin transporters,” <i>Nature Communications</i>, vol. 6. Nature Publishing Group,
    2015.
  ista: Šimášková M, O’Brien J, Khan-Djamei M, Van Noorden G, Ötvös K, Vieten A, De
    Clercq I, Van Haperen J, Cuesta C, Hoyerová K, Vanneste S, Marhavý P, Wabnik KT,
    Van Breusegem F, Nowack M, Murphy A, Friml J, Weijers D, Beeckman T, Benková E.
    2015. Cytokinin response factors regulate PIN-FORMED auxin transporters. Nature
    Communications. 6, 8717.
  mla: Šimášková, Mária, et al. “Cytokinin Response Factors Regulate PIN-FORMED Auxin
    Transporters.” <i>Nature Communications</i>, vol. 6, 8717, Nature Publishing Group,
    2015, doi:<a href="https://doi.org/10.1038/ncomms9717">10.1038/ncomms9717</a>.
  short: M. Šimášková, J. O’Brien, M. Khan-Djamei, G. Van Noorden, K. Ötvös, A. Vieten,
    I. De Clercq, J. Van Haperen, C. Cuesta, K. Hoyerová, S. Vanneste, P. Marhavý,
    K.T. Wabnik, F. Van Breusegem, M. Nowack, A. Murphy, J. Friml, D. Weijers, T.
    Beeckman, E. Benková, Nature Communications 6 (2015).
corr_author: '1'
date_created: 2018-12-11T11:53:12Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2025-09-23T08:24:11Z
day: '01'
ddc:
- '580'
department:
- _id: EvBe
- _id: JiFr
doi: 10.1038/ncomms9717
ec_funded: 1
external_id:
  isi:
  - '000366289800001'
file:
- access_level: open_access
  checksum: c2c84bca37401435fedf76bad0ba0579
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:18:36Z
  date_updated: 2020-07-14T12:45:08Z
  file_id: '5358'
  file_name: IST-2018-1020-v1+1_Simaskova_et_al_NatCom_2015.pdf
  file_size: 1471217
  relation: main_file
file_date_updated: 2020-07-14T12:45:08Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
project:
- _id: 253FCA6A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '207362'
  name: Hormonal cross-talk in plant organogenesis
- _id: 2542D156-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I 1774-B16
  name: Hormone cross-talk drives nutrient dependent plant development
publication: Nature Communications
publication_status: published
publisher: Nature Publishing Group
publist_id: '5513'
pubrep_id: '1020'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cytokinin response factors regulate PIN-FORMED auxin transporters
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 6
year: '2015'
...
---
_id: '1847'
acknowledgement: This work was supported by the European Research Council (project
  ERC-2011-StG-20101109-PSDP), European Social Fund (CZ.1.07/2.3.00/20.0043), and
  the Czech Science Foundation GAČR (GA13-40637S).
article_processing_charge: No
author:
- first_name: Peter
  full_name: Grones, Peter
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- first_name: Jiřĺ
  full_name: Friml, Jiřĺ
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Grones P, Friml J. ABP1: Finally docking. <i>Molecular Plant</i>. 2015;8(3):356-358.
    doi:<a href="https://doi.org/10.1016/j.molp.2014.12.013">10.1016/j.molp.2014.12.013</a>'
  apa: 'Grones, P., &#38; Friml, J. (2015). ABP1: Finally docking. <i>Molecular Plant</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.molp.2014.12.013">https://doi.org/10.1016/j.molp.2014.12.013</a>'
  chicago: 'Grones, Peter, and Jiří Friml. “ABP1: Finally Docking.” <i>Molecular Plant</i>.
    Elsevier, 2015. <a href="https://doi.org/10.1016/j.molp.2014.12.013">https://doi.org/10.1016/j.molp.2014.12.013</a>.'
  ieee: 'P. Grones and J. Friml, “ABP1: Finally docking,” <i>Molecular Plant</i>,
    vol. 8, no. 3. Elsevier, pp. 356–358, 2015.'
  ista: 'Grones P, Friml J. 2015. ABP1: Finally docking. Molecular Plant. 8(3), 356–358.'
  mla: 'Grones, Peter, and Jiří Friml. “ABP1: Finally Docking.” <i>Molecular Plant</i>,
    vol. 8, no. 3, Elsevier, 2015, pp. 356–58, doi:<a href="https://doi.org/10.1016/j.molp.2014.12.013">10.1016/j.molp.2014.12.013</a>.'
  short: P. Grones, J. Friml, Molecular Plant 8 (2015) 356–358.
corr_author: '1'
date_created: 2018-12-11T11:54:20Z
date_published: 2015-03-02T00:00:00Z
date_updated: 2025-09-23T07:30:08Z
day: '02'
department:
- _id: JiFr
doi: 10.1016/j.molp.2014.12.013
external_id:
  isi:
  - '000350813400003'
intvolume: '         8'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa_version: None
page: 356 - 358
publication: Molecular Plant
publication_status: published
publisher: Elsevier
publist_id: '5254'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'ABP1: Finally docking'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 8
year: '2015'
...
---
_id: '1849'
abstract:
- lang: eng
  text: 'Cell polarity is a fundamental property of pro- and eukaryotic cells. It
    is necessary for coordination of cell division, cell morphogenesis and signaling
    processes. How polarity is generated and maintained is a complex issue governed
    by interconnected feed-back regulations between small GTPase signaling and membrane
    tension-based signaling that controls membrane trafficking, and cytoskeleton organization
    and dynamics. Here, we will review the potential role for calcium as a crucial
    signal that connects and coordinates the respective processes during polarization
    processes in plants. This article is part of a Special Issue entitled: 13th European
    Symposium on Calcium.'
acknowledgement: The contributing authors were supported by the Ghent University Special
  Research Fund (to E.H.), the Interuniversity Attraction Poles Programme (IAP VI/33
  and IUAP P7/29 ‘MARS’), the European Research Council (project ERC-2011-StG-20101109-PSDP,
  to J.F.), and the Research Foundation Flanders (to S.V.).
article_processing_charge: No
author:
- first_name: Ellie
  full_name: Himschoot, Ellie
  last_name: Himschoot
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Jiřĺ
  full_name: Friml, Jiřĺ
  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: Himschoot E, Beeckman T, Friml J, Vanneste S. Calcium is an organizer of cell
    polarity in plants. <i>Biochimica et Biophysica Acta - Molecular Cell Research</i>.
    2015;1853(9):2168-2172. doi:<a href="https://doi.org/10.1016/j.bbamcr.2015.02.017">10.1016/j.bbamcr.2015.02.017</a>
  apa: Himschoot, E., Beeckman, T., Friml, J., &#38; Vanneste, S. (2015). Calcium
    is an organizer of cell polarity in plants. <i>Biochimica et Biophysica Acta -
    Molecular Cell Research</i>. Elsevier. <a href="https://doi.org/10.1016/j.bbamcr.2015.02.017">https://doi.org/10.1016/j.bbamcr.2015.02.017</a>
  chicago: Himschoot, Ellie, Tom Beeckman, Jiří Friml, and Steffen Vanneste. “Calcium
    Is an Organizer of Cell Polarity in Plants.” <i>Biochimica et Biophysica Acta
    - Molecular Cell Research</i>. Elsevier, 2015. <a href="https://doi.org/10.1016/j.bbamcr.2015.02.017">https://doi.org/10.1016/j.bbamcr.2015.02.017</a>.
  ieee: E. Himschoot, T. Beeckman, J. Friml, and S. Vanneste, “Calcium is an organizer
    of cell polarity in plants,” <i>Biochimica et Biophysica Acta - Molecular Cell
    Research</i>, vol. 1853, no. 9. Elsevier, pp. 2168–2172, 2015.
  ista: Himschoot E, Beeckman T, Friml J, Vanneste S. 2015. Calcium is an organizer
    of cell polarity in plants. Biochimica et Biophysica Acta - Molecular Cell Research.
    1853(9), 2168–2172.
  mla: Himschoot, Ellie, et al. “Calcium Is an Organizer of Cell Polarity in Plants.”
    <i>Biochimica et Biophysica Acta - Molecular Cell Research</i>, vol. 1853, no.
    9, Elsevier, 2015, pp. 2168–72, doi:<a href="https://doi.org/10.1016/j.bbamcr.2015.02.017">10.1016/j.bbamcr.2015.02.017</a>.
  short: E. Himschoot, T. Beeckman, J. Friml, S. Vanneste, Biochimica et Biophysica
    Acta - Molecular Cell Research 1853 (2015) 2168–2172.
date_created: 2018-12-11T11:54:21Z
date_published: 2015-09-01T00:00:00Z
date_updated: 2025-09-23T08:04:01Z
day: '01'
department:
- _id: JiFr
doi: 10.1016/j.bbamcr.2015.02.017
external_id:
  isi:
  - '000359960400028'
intvolume: '      1853'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa_version: None
page: 2168 - 2172
publication: Biochimica et Biophysica Acta - Molecular Cell Research
publication_status: published
publisher: Elsevier
publist_id: '5252'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Calcium is an organizer of cell polarity in plants
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 1853
year: '2015'
...
---
_id: '1865'
abstract:
- lang: eng
  text: The plant hormone auxin and its directional transport are known to play a
    crucial role in defining the embryonic axis and subsequent development of the
    body plan. Although the role of PIN auxin efflux transporters has been clearly
    assigned during embryonic shoot and root specification, the role of the auxin
    influx carriers AUX1 and LIKE-AUX1 (LAX) proteins is not well established. Here,
    we used chemical and genetic tools on Brassica napus microspore-derived embryos
    and Arabidopsis thaliana zygotic embryos, and demonstrate that AUX1, LAX1 and
    LAX2 are required for both shoot and root pole formation, in concert with PIN
    efflux carriers. Furthermore, we uncovered a positive-feedback loop betweenMONOPTEROS(ARF5)-dependent
    auxin signalling and auxin transport. ThisMONOPTEROSdependent transcriptional
    regulation of auxin influx (AUX1, LAX1 and LAX2) and auxin efflux (PIN1 and PIN4)
    carriers by MONOPTEROS helps to maintain proper auxin transport to the root tip.
    These results indicate that auxin-dependent cell specification during embryo development
    requires balanced auxin transport involving both influx and efflux mechanisms,
    and that this transport is maintained by a positive transcriptional feedback on
    auxin signalling.
acknowledgement: W.G. is a post-doctoral fellow of the Research Foundation Flanders.
  H.S.R. is supported by Employment of Best Young Scientists for International Cooperation
  Empowerment [CZ.1.07/2.3.00/30.0037], co-financed by the European Social Fund and
  the state budget of the Czech Republic. Mi.S. was funded by the Ramón y Cajal program.
  This work was supported by the European Research Council [project ERC-2011-StG-20101109-PSDP],
  project ‘CEITEC – Central European Institute of Technology’ [CZ.1.05/1.1.00/02.0068],
  the European Social Fund [CZ.1.07/2.3.00/20.0043] and the Czech Science Foundation
  GACR [GA13-40637S] to J.F. We acknowledge funding from the Biological and Biotechnological
  Science Research Council (BBSRC) and Engineering Physics Science Research Council
  (EPSRC) to R.S. and M.B
article_processing_charge: No
author:
- first_name: Hélène
  full_name: Robert, Hélène
  last_name: Robert
- first_name: Wim
  full_name: Grunewald, Wim
  last_name: Grunewald
- first_name: Michael
  full_name: Sauer, Michael
  last_name: Sauer
- first_name: Bernard
  full_name: Cannoot, Bernard
  last_name: Cannoot
- first_name: Mercedes
  full_name: Soriano, Mercedes
  last_name: Soriano
- first_name: Ranjan
  full_name: Swarup, Ranjan
  last_name: Swarup
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Malcolm
  full_name: Bennett, Malcolm
  last_name: Bennett
- first_name: Kim
  full_name: Boutilier, Kim
  last_name: Boutilier
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Robert H, Grunewald W, Sauer M, et al. Plant embryogenesis requires AUX/LAX-mediated
    auxin influx. <i>Development</i>. 2015;142(4):702-711. doi:<a href="https://doi.org/10.1242/dev.115832">10.1242/dev.115832</a>
  apa: Robert, H., Grunewald, W., Sauer, M., Cannoot, B., Soriano, M., Swarup, R.,
    … Friml, J. (2015). Plant embryogenesis requires AUX/LAX-mediated auxin influx.
    <i>Development</i>. Company of Biologists. <a href="https://doi.org/10.1242/dev.115832">https://doi.org/10.1242/dev.115832</a>
  chicago: Robert, Hélène, Wim Grunewald, Michael Sauer, Bernard Cannoot, Mercedes
    Soriano, Ranjan Swarup, Dolf Weijers, Malcolm Bennett, Kim Boutilier, and Jiří
    Friml. “Plant Embryogenesis Requires AUX/LAX-Mediated Auxin Influx.” <i>Development</i>.
    Company of Biologists, 2015. <a href="https://doi.org/10.1242/dev.115832">https://doi.org/10.1242/dev.115832</a>.
  ieee: H. Robert <i>et al.</i>, “Plant embryogenesis requires AUX/LAX-mediated auxin
    influx,” <i>Development</i>, vol. 142, no. 4. Company of Biologists, pp. 702–711,
    2015.
  ista: Robert H, Grunewald W, Sauer M, Cannoot B, Soriano M, Swarup R, Weijers D,
    Bennett M, Boutilier K, Friml J. 2015. Plant embryogenesis requires AUX/LAX-mediated
    auxin influx. Development. 142(4), 702–711.
  mla: Robert, Hélène, et al. “Plant Embryogenesis Requires AUX/LAX-Mediated Auxin
    Influx.” <i>Development</i>, vol. 142, no. 4, Company of Biologists, 2015, pp.
    702–11, doi:<a href="https://doi.org/10.1242/dev.115832">10.1242/dev.115832</a>.
  short: H. Robert, W. Grunewald, M. Sauer, B. Cannoot, M. Soriano, R. Swarup, D.
    Weijers, M. Bennett, K. Boutilier, J. Friml, Development 142 (2015) 702–711.
corr_author: '1'
date_created: 2018-12-11T11:54:26Z
date_published: 2015-02-15T00:00:00Z
date_updated: 2025-09-23T09:50:13Z
day: '15'
department:
- _id: JiFr
doi: 10.1242/dev.115832
ec_funded: 1
external_id:
  isi:
  - '000351697100011'
intvolume: '       142'
isi: 1
issue: '4'
language:
- iso: eng
month: '02'
oa_version: None
page: 702 - 711
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '5231'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Plant embryogenesis requires AUX/LAX-mediated auxin influx
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 142
year: '2015'
...
---
_id: '1871'
abstract:
- lang: eng
  text: The plant hormone auxin is a key regulator of plant growth and development.
    Differences in auxin distribution within tissues are mediated by the polar auxin
    transport machinery, and cellular auxin responses occur depending on changes in
    cellular auxin levels. Multiple receptor systems at the cell surface and in the
    interior operate to sense and interpret fluctuations in auxin distribution that
    occur during plant development. Until now, three proteins or protein complexes
    that can bind auxin have been identified. SCFTIR1 [a SKP1-cullin-1-F-box complex
    that contains transport inhibitor response 1 (TIR1) as the F-box protein] and
    S-phase-kinaseassociated protein 2 (SKP2) localize to the nucleus, whereas auxinbinding
    protein 1 (ABP1), predominantly associates with the endoplasmic reticulum and
    cell surface. In this Cell Science at a Glance article, we summarize recent discoveries
    in the field of auxin transport and signaling that have led to the identification
    of new components of these pathways, as well as their mutual interaction.
acknowledgement: This work was supported by the European Research Council [project
  ERC-2011-StG-20101109-PSDP]; European Social Fund [grant number CZ.1.07/2.3.00/20.0043]
  and the Czech Science Foundation GAČR [grant number GA13-40637S]
article_processing_charge: No
author:
- first_name: Peter
  full_name: Grones, Peter
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- 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, Friml J. Auxin transporters and binding proteins at a glance. <i>Journal
    of Cell Science</i>. 2015;128(1):1-7. doi:<a href="https://doi.org/10.1242/jcs.159418">10.1242/jcs.159418</a>
  apa: Grones, P., &#38; Friml, J. (2015). Auxin transporters and binding proteins
    at a glance. <i>Journal of Cell Science</i>. Company of Biologists. <a href="https://doi.org/10.1242/jcs.159418">https://doi.org/10.1242/jcs.159418</a>
  chicago: Grones, Peter, and Jiří Friml. “Auxin Transporters and Binding Proteins
    at a Glance.” <i>Journal of Cell Science</i>. Company of Biologists, 2015. <a
    href="https://doi.org/10.1242/jcs.159418">https://doi.org/10.1242/jcs.159418</a>.
  ieee: P. Grones and J. Friml, “Auxin transporters and binding proteins at a glance,”
    <i>Journal of Cell Science</i>, vol. 128, no. 1. Company of Biologists, pp. 1–7,
    2015.
  ista: Grones P, Friml J. 2015. Auxin transporters and binding proteins at a glance.
    Journal of Cell Science. 128(1), 1–7.
  mla: Grones, Peter, and Jiří Friml. “Auxin Transporters and Binding Proteins at
    a Glance.” <i>Journal of Cell Science</i>, vol. 128, no. 1, Company of Biologists,
    2015, pp. 1–7, doi:<a href="https://doi.org/10.1242/jcs.159418">10.1242/jcs.159418</a>.
  short: P. Grones, J. Friml, Journal of Cell Science 128 (2015) 1–7.
corr_author: '1'
date_created: 2018-12-11T11:54:28Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2025-09-23T07:58:34Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1242/jcs.159418
external_id:
  isi:
  - '000347167200001'
file:
- access_level: open_access
  checksum: 24c779f4cd9d549ca6833e26f486be27
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:11:00Z
  date_updated: 2020-07-14T12:45:19Z
  file_id: '4852'
  file_name: IST-2016-563-v1+1_1.full.pdf
  file_size: 1688844
  relation: main_file
file_date_updated: 2020-07-14T12:45:19Z
has_accepted_license: '1'
intvolume: '       128'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
page: 1 - 7
publication: Journal of Cell Science
publication_status: published
publisher: Company of Biologists
publist_id: '5225'
pubrep_id: '563'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Auxin transporters and binding proteins at a glance
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 128
year: '2015'
...
---
_id: '1878'
abstract:
- lang: eng
  text: Petrocoptis is a small genus of chasmophytic plants endemic to the Iberian
    Peninsula, with some localized populations in the French Pyrenees. Within the
    genus, a dozen species have been recognized based on morphological diversity,
    most of them with limited distribution area, in small populations and frequently
    with potential threats to their survival. To date, however, a molecular evaluation
    of the current systematic treatments has not been carried out. The aim of the
    present study is to infer phylogenetic relationships among its subordinate taxa
    by using plastidial rps16 intron and nuclear internal transcribed spacer (ITS)
    DNA sequences; and evaluate the phylogenetic placement of the genus Petrocoptis
    within the family Caryophyllaceae. The monophyly of Petrocoptis is supported by
    both ITS and rps16 intron sequence analyses. Furthermore, time estimates using
    BEAST analyses indicate a Middle to Late Miocene diversification (10.59 Myr, 6.44–15.26
    Myr highest posterior densities [HPD], for ITS; 14.30 Myr, 8.61–21.00 Myr HPD,
    for rps16 intron).
article_processing_charge: No
author:
- first_name: Eduardo
  full_name: Cires Rodriguez, Eduardo
  id: 2AD56A7A-F248-11E8-B48F-1D18A9856A87
  last_name: Cires Rodriguez
- first_name: José
  full_name: Prieto, José
  last_name: Prieto
citation:
  ama: Cires Rodriguez E, Prieto J. Phylogenetic relationships of Petrocoptis A. Braun
    ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula. <i>Journal
    of Plant Research</i>. 2015;128(2):223-238. doi:<a href="https://doi.org/10.1007/s10265-014-0691-6">10.1007/s10265-014-0691-6</a>
  apa: Cires Rodriguez, E., &#38; Prieto, J. (2015). Phylogenetic relationships of
    Petrocoptis A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian
    Peninsula. <i>Journal of Plant Research</i>. Springer. <a href="https://doi.org/10.1007/s10265-014-0691-6">https://doi.org/10.1007/s10265-014-0691-6</a>
  chicago: Cires Rodriguez, Eduardo, and José Prieto. “Phylogenetic Relationships
    of Petrocoptis A. Braun Ex Endl. (Caryophyllaceae), a Discussed Genus from the
    Iberian Peninsula.” <i>Journal of Plant Research</i>. Springer, 2015. <a href="https://doi.org/10.1007/s10265-014-0691-6">https://doi.org/10.1007/s10265-014-0691-6</a>.
  ieee: E. Cires Rodriguez and J. Prieto, “Phylogenetic relationships of Petrocoptis
    A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula,”
    <i>Journal of Plant Research</i>, vol. 128, no. 2. Springer, pp. 223–238, 2015.
  ista: Cires Rodriguez E, Prieto J. 2015. Phylogenetic relationships of Petrocoptis
    A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula.
    Journal of Plant Research. 128(2), 223–238.
  mla: Cires Rodriguez, Eduardo, and José Prieto. “Phylogenetic Relationships of Petrocoptis
    A. Braun Ex Endl. (Caryophyllaceae), a Discussed Genus from the Iberian Peninsula.”
    <i>Journal of Plant Research</i>, vol. 128, no. 2, Springer, 2015, pp. 223–38,
    doi:<a href="https://doi.org/10.1007/s10265-014-0691-6">10.1007/s10265-014-0691-6</a>.
  short: E. Cires Rodriguez, J. Prieto, Journal of Plant Research 128 (2015) 223–238.
corr_author: '1'
date_created: 2018-12-11T11:54:30Z
date_published: 2015-01-24T00:00:00Z
date_updated: 2025-09-23T09:49:04Z
day: '24'
department:
- _id: JiFr
doi: 10.1007/s10265-014-0691-6
external_id:
  isi:
  - '000350826000001'
intvolume: '       128'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa_version: None
page: 223 - 238
publication: Journal of Plant Research
publication_status: published
publisher: Springer
publist_id: '5217'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Phylogenetic relationships of Petrocoptis A. Braun ex Endl. (Caryophyllaceae),
  a discussed genus from the Iberian Peninsula
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 128
year: '2015'
...
---
_id: '1879'
abstract:
- lang: eng
  text: When electron microscopy (EM) was introduced in the 1930s it gave scientists
    their first look into the nanoworld of cells. Over the last 80 years EM has vastly
    increased our understanding of the complex cellular structures that underlie the
    diverse functions that cells need to maintain life. One drawback that has been
    difficult to overcome was the inherent lack of volume information, mainly due
    to the limit on the thickness of sections that could be viewed in a transmission
    electron microscope (TEM). For many years scientists struggled to achieve three-dimensional
    (3D) EM using serial section reconstructions, TEM tomography, and scanning EM
    (SEM) techniques such as freeze-fracture. Although each technique yielded some
    special information, they required a significant amount of time and specialist
    expertise to obtain even a very small 3D EM dataset. Almost 20 years ago scientists
    began to exploit SEMs to image blocks of embedded tissues and perform serial sectioning
    of these tissues inside the SEM chamber. Using first focused ion beams (FIB) and
    subsequently robotic ultramicrotomes (serial block-face, SBF-SEM) microscopists
    were able to collect large volumes of 3D EM information at resolutions that could
    address many important biological questions, and do so in an efficient manner.
    We present here some examples of 3D EM taken from the many diverse specimens that
    have been imaged in our core facility. We propose that the next major step forward
    will be to efficiently correlate functional information obtained using light microscopy
    (LM) with 3D EM datasets to more completely investigate the important links between
    cell structures and their functions.
acknowledgement: The Zeiss Merlin with Gatan 3View2XP and Zeiss Auriga were acquired
  through a CLEM grant from Minister Ingrid Lieten to the VIB Bio-Imaging-Core. Michiel
  Krols and Saskia Lippens are the recipients of a fellowship from the FWO (Fonds
  Wetenschappelijk Onderzoek) of Flanders.
article_processing_charge: No
author:
- first_name: A
  full_name: Kremer, A
  last_name: Kremer
- first_name: Stefaan
  full_name: Lippens, Stefaan
  last_name: Lippens
- first_name: Sonia
  full_name: Bartunkova, Sonia
  last_name: Bartunkova
- first_name: Bob
  full_name: Asselbergh, Bob
  last_name: Asselbergh
- first_name: Cendric
  full_name: Blanpain, Cendric
  last_name: Blanpain
- first_name: Matyas
  full_name: Fendrych, Matyas
  id: 43905548-F248-11E8-B48F-1D18A9856A87
  last_name: Fendrych
  orcid: 0000-0002-9767-8699
- first_name: A
  full_name: Goossens, A
  last_name: Goossens
- first_name: Matthew
  full_name: Holt, Matthew
  last_name: Holt
- first_name: Sophie
  full_name: Janssens, Sophie
  last_name: Janssens
- first_name: Michiel
  full_name: Krols, Michiel
  last_name: Krols
- first_name: Jean
  full_name: Larsimont, Jean
  last_name: Larsimont
- first_name: Conor
  full_name: Mc Guire, Conor
  last_name: Mc Guire
- first_name: Moritz
  full_name: Nowack, Moritz
  last_name: Nowack
- first_name: Xavier
  full_name: Saelens, Xavier
  last_name: Saelens
- first_name: Andreas
  full_name: Schertel, Andreas
  last_name: Schertel
- first_name: B
  full_name: Schepens, B
  last_name: Schepens
- first_name: M
  full_name: Slezak, M
  last_name: Slezak
- first_name: Vincent
  full_name: Timmerman, Vincent
  last_name: Timmerman
- first_name: Clara
  full_name: Theunis, Clara
  last_name: Theunis
- first_name: Ronald
  full_name: Van Brempt, Ronald
  last_name: Van Brempt
- first_name: Y
  full_name: Visser, Y
  last_name: Visser
- first_name: Christophe
  full_name: Guérin, Christophe
  last_name: Guérin
citation:
  ama: Kremer A, Lippens S, Bartunkova S, et al. Developing 3D SEM in a broad biological
    context. <i>Journal of Microscopy</i>. 2015;259(2):80-96. doi:<a href="https://doi.org/10.1111/jmi.12211">10.1111/jmi.12211</a>
  apa: Kremer, A., Lippens, S., Bartunkova, S., Asselbergh, B., Blanpain, C., Fendrych,
    M., … Guérin, C. (2015). Developing 3D SEM in a broad biological context. <i>Journal
    of Microscopy</i>. Wiley-Blackwell. <a href="https://doi.org/10.1111/jmi.12211">https://doi.org/10.1111/jmi.12211</a>
  chicago: Kremer, A, Stefaan Lippens, Sonia Bartunkova, Bob Asselbergh, Cendric Blanpain,
    Matyas Fendrych, A Goossens, et al. “Developing 3D SEM in a Broad Biological Context.”
    <i>Journal of Microscopy</i>. Wiley-Blackwell, 2015. <a href="https://doi.org/10.1111/jmi.12211">https://doi.org/10.1111/jmi.12211</a>.
  ieee: A. Kremer <i>et al.</i>, “Developing 3D SEM in a broad biological context,”
    <i>Journal of Microscopy</i>, vol. 259, no. 2. Wiley-Blackwell, pp. 80–96, 2015.
  ista: Kremer A, Lippens S, Bartunkova S, Asselbergh B, Blanpain C, Fendrych M, Goossens
    A, Holt M, Janssens S, Krols M, Larsimont J, Mc Guire C, Nowack M, Saelens X,
    Schertel A, Schepens B, Slezak M, Timmerman V, Theunis C, Van Brempt R, Visser
    Y, Guérin C. 2015. Developing 3D SEM in a broad biological context. Journal of
    Microscopy. 259(2), 80–96.
  mla: Kremer, A., et al. “Developing 3D SEM in a Broad Biological Context.” <i>Journal
    of Microscopy</i>, vol. 259, no. 2, Wiley-Blackwell, 2015, pp. 80–96, doi:<a href="https://doi.org/10.1111/jmi.12211">10.1111/jmi.12211</a>.
  short: A. Kremer, S. Lippens, S. Bartunkova, B. Asselbergh, C. Blanpain, M. Fendrych,
    A. Goossens, M. Holt, S. Janssens, M. Krols, J. Larsimont, C. Mc Guire, M. Nowack,
    X. Saelens, A. Schertel, B. Schepens, M. Slezak, V. Timmerman, C. Theunis, R.
    Van Brempt, Y. Visser, C. Guérin, Journal of Microscopy 259 (2015) 80–96.
date_created: 2018-12-11T11:54:30Z
date_published: 2015-08-01T00:00:00Z
date_updated: 2025-09-23T08:26:17Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1111/jmi.12211
external_id:
  isi:
  - '000358300600002'
file:
- access_level: open_access
  checksum: 3649c5372d1644062d728ea9287e367f
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:11:19Z
  date_updated: 2020-07-14T12:45:19Z
  file_id: '4872'
  file_name: IST-2016-459-v1+1_KREMER_et_al-2015-Journal_of_Microscopy.pdf
  file_size: 2899898
  relation: main_file
file_date_updated: 2020-07-14T12:45:19Z
has_accepted_license: '1'
intvolume: '       259'
isi: 1
issue: '2'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 80 - 96
publication: Journal of Microscopy
publication_status: published
publisher: Wiley-Blackwell
publist_id: '5218'
pubrep_id: '459'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Developing 3D SEM in a broad biological context
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 259
year: '2015'
...
