---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '21716'
abstract:
- lang: eng
  text: Male germline development in plants is highly sensitive to heat stress, with
    elevated temperatures frequently impairing male fertility and consequently reducing
    seed production. Indeed, recent global warming has decreased major crop yields,
    emphasizing the urgent need to elucidate the molecular and cellular mechanisms
    underlying heat-induced male sterility. This review synthesizes current knowledge
    on how heat stress disrupts microsporogenesis and microgametogenesis, and how
    plants counteract these stresses through diverse thermotolerance mechanisms. We
    emphasize temperature-sensitive processes, including meiotic progression in male
    germ cells, programmed cell death of somatic tapetal nurse cells, and post-meiotic
    pollen tube development. We further discuss how epigenetic regulators enhance
    thermotolerance by reprogramming DNA methylation landscapes and modulating histone
    variant distribution. Finally, we propose future directions aimed at understanding
    the mechanisms of reproductive thermotolerance from the epigenetic perspective.
acknowledgement: This work was supported by JSPS KAKENHI (grant number JP22J01430)
  and the Osamu Hayaishi Memorial Scholarship for Study Abroad for H.N.
article_number: '102881'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Hiroki
  full_name: Nagai, Hiroki
  id: 608df3e6-e2ab-11ed-8890-c9318cec7da4
  last_name: Nagai
  orcid: 0000-0003-1671-9434
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: NAGAI H, Feng X. Genetic and epigenetic mechanisms underlying male reproductive
    thermotolerance. <i>Current Opinion in Plant Biology</i>. 2026;91(6). doi:<a href="https://doi.org/10.1016/j.pbi.2026.102881">10.1016/j.pbi.2026.102881</a>
  apa: NAGAI, H., &#38; Feng, X. (2026). Genetic and epigenetic mechanisms underlying
    male reproductive thermotolerance. <i>Current Opinion in Plant Biology</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.pbi.2026.102881">https://doi.org/10.1016/j.pbi.2026.102881</a>
  chicago: NAGAI, HIROKI, and Xiaoqi Feng. “Genetic and Epigenetic Mechanisms Underlying
    Male Reproductive Thermotolerance.” <i>Current Opinion in Plant Biology</i>. Elsevier,
    2026. <a href="https://doi.org/10.1016/j.pbi.2026.102881">https://doi.org/10.1016/j.pbi.2026.102881</a>.
  ieee: H. NAGAI and X. Feng, “Genetic and epigenetic mechanisms underlying male reproductive
    thermotolerance,” <i>Current Opinion in Plant Biology</i>, vol. 91, no. 6. Elsevier,
    2026.
  ista: NAGAI H, Feng X. 2026. Genetic and epigenetic mechanisms underlying male reproductive
    thermotolerance. Current Opinion in Plant Biology. 91(6), 102881.
  mla: NAGAI, HIROKI, and Xiaoqi Feng. “Genetic and Epigenetic Mechanisms Underlying
    Male Reproductive Thermotolerance.” <i>Current Opinion in Plant Biology</i>, vol.
    91, no. 6, 102881, Elsevier, 2026, doi:<a href="https://doi.org/10.1016/j.pbi.2026.102881">10.1016/j.pbi.2026.102881</a>.
  short: H. NAGAI, X. Feng, Current Opinion in Plant Biology 91 (2026).
corr_author: '1'
date_created: 2026-04-12T22:01:50Z
date_published: 2026-04-01T00:00:00Z
date_updated: 2026-05-04T11:15:57Z
day: '01'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.1016/j.pbi.2026.102881
has_accepted_license: '1'
intvolume: '        91'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.pbi.2026.102881
month: '04'
oa: 1
oa_version: Published Version
publication: Current Opinion in Plant Biology
publication_identifier:
  eissn:
  - 1879-0356
  issn:
  - 1369-5266
publication_status: epub_ahead
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Genetic and epigenetic mechanisms underlying male reproductive thermotolerance
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: 91
year: '2026'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '20220'
abstract:
- lang: eng
  text: Stress granules (SG) are biomolecular condensates that represent an adaptive
    response of cells to various stresses, including heat. However, the cell type–specific
    function and relevance of SG formation, especially during reproductive development,
    are largely not understood. Here, we show that the meiotic A-type cyclin TARDY
    ASYNCHRONOUS MEIOSIS (TAM) is recruited to SGs in male meiocytes of Arabidopsis
    after exposure to heat. We find that the amino terminus of TAM is necessary and
    sufficient for the localization of proteins to meiotic SGs. Swapping the amino
    terminus of TAM with the one of its sister protein CYCA1;1 resulted in a separation-of-function
    allele of TAM, which prevents the partitioning of TAM to SGs while restoring a
    wild-type phenotype in a tam mutant background under nonheat stress conditions.
    Notably, plants expressing this TAM version prematurely terminate meiosis under
    heat resulting in unreduced gametes. Thus, the formation of TAM-containing SGs
    is necessary for genome stability under heat stress.
acknowledged_ssus:
- _id: Bio
acknowledgement: "We thank L. Strader (Duke University, Durham) and A. Holehouse (Washington
  University, Saint Louis) for discussion and input in LLPS. We thank T. Nakagawa
  (Shimane University, Matsue) for providing the pGWB604 Gateway vector containing
  bar gene identified by Meiji Seika Kaisha Ltd. We thank M. Heese (Hamburg University)
  for the critical reading and comments on this manuscript. We further thank J. Mehrmann
  (Hamburg University) for technical assistance. We thank the ISTA imaging facility
  for assistance for microscopy.\r\nThis project has received funding from JST-PRESTO
  (JPMJPR18H7), JST-CREST (JPMJCR18H4), European Union’s Horizon 2020 under MSCA grant
  101034413, and a federal grant from the state of Hamburg (LFF-BiCon)."
article_processing_charge: Yes
article_type: original
author:
- first_name: Joke G
  full_name: De Jaeger-Braet, Joke G
  id: 26bd38d3-c59a-11ee-a1af-d7a988cafcc5
  last_name: De Jaeger-Braet
- first_name: Merle
  full_name: Hartmann, Merle
  last_name: Hartmann
- first_name: Lev
  full_name: Böttger, Lev
  last_name: Böttger
- first_name: Chao
  full_name: Yang, Chao
  id: 082e3e6e-8069-11ed-8390-c8cce7b1aaca
  last_name: Yang
- first_name: Takahiro
  full_name: Hamada, Takahiro
  last_name: Hamada
- first_name: Stefan
  full_name: Hoth, Stefan
  last_name: Hoth
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Magdalena
  full_name: Weingartner, Magdalena
  last_name: Weingartner
- first_name: Arp
  full_name: Schnittger, Arp
  last_name: Schnittger
citation:
  ama: De Jaeger-Braet JG, Hartmann M, Böttger L, et al. The recruitment of the A-type
    cyclin TAM to stress granules is crucial for meiotic fidelity under heat. <i>Science
    Advances</i>. 2025;11(32):eadr5694. doi:<a href="https://doi.org/10.1126/sciadv.adr5694">10.1126/sciadv.adr5694</a>
  apa: De Jaeger-Braet, J. G., Hartmann, M., Böttger, L., Yang, C., Hamada, T., Hoth,
    S., … Schnittger, A. (2025). The recruitment of the A-type cyclin TAM to stress
    granules is crucial for meiotic fidelity under heat. <i>Science Advances</i>.
    AAAS. <a href="https://doi.org/10.1126/sciadv.adr5694">https://doi.org/10.1126/sciadv.adr5694</a>
  chicago: De Jaeger-Braet, Joke G, Merle Hartmann, Lev Böttger, Chao Yang, Takahiro
    Hamada, Stefan Hoth, Xiaoqi Feng, Magdalena Weingartner, and Arp Schnittger. “The
    Recruitment of the A-Type Cyclin TAM to Stress Granules Is Crucial for Meiotic
    Fidelity under Heat.” <i>Science Advances</i>. AAAS, 2025. <a href="https://doi.org/10.1126/sciadv.adr5694">https://doi.org/10.1126/sciadv.adr5694</a>.
  ieee: J. G. De Jaeger-Braet <i>et al.</i>, “The recruitment of the A-type cyclin
    TAM to stress granules is crucial for meiotic fidelity under heat,” <i>Science
    Advances</i>, vol. 11, no. 32. AAAS, p. eadr5694, 2025.
  ista: De Jaeger-Braet JG, Hartmann M, Böttger L, Yang C, Hamada T, Hoth S, Feng
    X, Weingartner M, Schnittger A. 2025. The recruitment of the A-type cyclin TAM
    to stress granules is crucial for meiotic fidelity under heat. Science Advances.
    11(32), eadr5694.
  mla: De Jaeger-Braet, Joke G., et al. “The Recruitment of the A-Type Cyclin TAM
    to Stress Granules Is Crucial for Meiotic Fidelity under Heat.” <i>Science Advances</i>,
    vol. 11, no. 32, AAAS, 2025, p. eadr5694, doi:<a href="https://doi.org/10.1126/sciadv.adr5694">10.1126/sciadv.adr5694</a>.
  short: J.G. De Jaeger-Braet, M. Hartmann, L. Böttger, C. Yang, T. Hamada, S. Hoth,
    X. Feng, M. Weingartner, A. Schnittger, Science Advances 11 (2025) eadr5694.
date_created: 2025-08-24T22:01:30Z
date_published: 2025-08-08T00:00:00Z
date_updated: 2025-09-30T14:24:10Z
day: '08'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.1126/sciadv.adr5694
ec_funded: 1
external_id:
  isi:
  - '001549102600016'
file:
- access_level: open_access
  checksum: 0f1ae246acc9b075f01bf4afe382c8ba
  content_type: application/pdf
  creator: dernst
  date_created: 2025-09-02T07:05:37Z
  date_updated: 2025-09-02T07:05:37Z
  file_id: '20270'
  file_name: 2025_ScienceAdvance_DeJaegerBraet.pdf
  file_size: 10876817
  relation: main_file
  success: 1
file_date_updated: 2025-09-02T07:05:37Z
has_accepted_license: '1'
intvolume: '        11'
isi: 1
issue: '32'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '08'
oa: 1
oa_version: Published Version
page: eadr5694
project:
- _id: fc2ed2f7-9c52-11eb-aca3-c01059dda49c
  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
publication: Science Advances
publication_identifier:
  eissn:
  - 2375-2548
publication_status: published
publisher: AAAS
quality_controlled: '1'
scopus_import: '1'
status: public
title: The recruitment of the A-type cyclin TAM to stress granules is crucial for
  meiotic fidelity under heat
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 11
year: '2025'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '19436'
abstract:
- lang: eng
  text: Dynamic DNA methylation represses transposable elements (TEs) and regulates
    gene activity, playing a pivotal role in plant development. Although substantial
    progress has been made in understanding DNA methylation reprogramming during germline
    development in Arabidopsis thaliana, whether similar mechanisms exist in other
    dicot plants remains unclear. Here, we analyzed DNA methylation levels in meiocytes,
    microspores, and pollens of Brassica Rapa using whole-genome bisulfite sequencing
    (WGBS). Global DNA methylation analysis revealed similar CHH methylation reprogramming
    compared to Arabidopsis, while distinct patterns were observed in the dynamics
    of global CG and CHG methylation in B. rapa. Differentially methylated region
    (DMR) analysis identified specifically methylated loci in the male sex cells of
    B. Rapa with a stronger tendency to target genes, similar to observations in Arabidopsis.
    Additionally, we found that the activity and genomic targeting preference of the
    small RNA-directed DNA methylation (RdDM) were altered during B. Rapa male germline
    development. A subset of long terminal repeat (LTR) TEs were activated, possibly
    due to the dynamic regulation of DNA methylation during male sexual development
    in B. Rapa. These findings provided new insights into the evolution of epigenetic
    reprogramming mechanisms in plants.
acknowledgement: We thank Prof. Ying Li of Nanjing Agricultural University for her
  help in providing seeds of K2 materials. This work was carried out with the support
  of National Natural Science Foundation of China (Grant No. 32070608).
article_number: '16'
article_processing_charge: Yes
article_type: original
author:
- first_name: Jun
  full_name: Zhang, Jun
  last_name: Zhang
- first_name: Di
  full_name: Wu, Di
  last_name: Wu
- first_name: Yating
  full_name: Zhang, Yating
  last_name: Zhang
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Hongbo
  full_name: Gao, Hongbo
  id: 77c2e73a-eabd-11ef-aee9-8093a2ba7a93
  last_name: Gao
citation:
  ama: Zhang J, Wu D, Zhang Y, Feng X, Gao H. DNA methylation dynamics in male germline
    development in Brassica Rapa. <i>Molecular Horticulture</i>. 2025;5. doi:<a href="https://doi.org/10.1186/s43897-024-00137-9">10.1186/s43897-024-00137-9</a>
  apa: Zhang, J., Wu, D., Zhang, Y., Feng, X., &#38; Gao, H. (2025). DNA methylation
    dynamics in male germline development in Brassica Rapa. <i>Molecular Horticulture</i>.
    Springer Nature. <a href="https://doi.org/10.1186/s43897-024-00137-9">https://doi.org/10.1186/s43897-024-00137-9</a>
  chicago: Zhang, Jun, Di Wu, Yating Zhang, Xiaoqi Feng, and Hongbo Gao. “DNA Methylation
    Dynamics in Male Germline Development in Brassica Rapa.” <i>Molecular Horticulture</i>.
    Springer Nature, 2025. <a href="https://doi.org/10.1186/s43897-024-00137-9">https://doi.org/10.1186/s43897-024-00137-9</a>.
  ieee: J. Zhang, D. Wu, Y. Zhang, X. Feng, and H. Gao, “DNA methylation dynamics
    in male germline development in Brassica Rapa,” <i>Molecular Horticulture</i>,
    vol. 5. Springer Nature, 2025.
  ista: Zhang J, Wu D, Zhang Y, Feng X, Gao H. 2025. DNA methylation dynamics in male
    germline development in Brassica Rapa. Molecular Horticulture. 5, 16.
  mla: Zhang, Jun, et al. “DNA Methylation Dynamics in Male Germline Development in
    Brassica Rapa.” <i>Molecular Horticulture</i>, vol. 5, 16, Springer Nature, 2025,
    doi:<a href="https://doi.org/10.1186/s43897-024-00137-9">10.1186/s43897-024-00137-9</a>.
  short: J. Zhang, D. Wu, Y. Zhang, X. Feng, H. Gao, Molecular Horticulture 5 (2025).
corr_author: '1'
date_created: 2025-03-23T23:01:25Z
date_published: 2025-03-04T00:00:00Z
date_updated: 2025-09-30T11:17:08Z
day: '04'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.1186/s43897-024-00137-9
external_id:
  isi:
  - '001436233900001'
  pmid:
  - '40033451'
file:
- access_level: open_access
  checksum: 6d1e0e9b0e1902e4a711f81c5c17a070
  content_type: application/pdf
  creator: dernst
  date_created: 2025-03-25T12:15:32Z
  date_updated: 2025-03-25T12:15:32Z
  file_id: '19460'
  file_name: 2025_MolecularHorticulture_Zhang.pdf
  file_size: 3014980
  relation: main_file
  success: 1
file_date_updated: 2025-03-25T12:15:32Z
has_accepted_license: '1'
intvolume: '         5'
isi: 1
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: Molecular Horticulture
publication_identifier:
  eissn:
  - 2730-9401
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA methylation dynamics in male germline development in Brassica Rapa
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: 5
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '19602'
abstract:
- lang: eng
  text: N4-methylcytosine (4mC) is an important DNA modification in prokaryotes, but
    its relevance and even its presence in eukaryotes have been mysterious. Here we
    show that spermatogenesis in the liverwort Marchantia polymorpha involves two
    waves of extensive DNA methylation reprogramming. First, 5-methylcytosine (5mC)
    expands from transposons to the entire genome. Notably, the second wave installs
    4mC throughout genic regions, covering over 50% of CG sites in sperm. 4mC requires
    a methyltransferase (MpDN4MT1a) that is specifically expressed during late spermiogenesis.
    Deletion of MpDN4MT1a alters the sperm transcriptome, causes sperm swimming and
    fertility defects, and impairs post-fertilization development. Our results reveal
    extensive 4mC in a eukaryote, identify a family of eukaryotic methyltransferases,
    and elucidate the biological functions of 4mC in reproductive development, thereby
    expanding the repertoire of functional eukaryotic DNA modifications.
acknowledged_ssus:
- _id: Bio
- _id: ScienComp
acknowledgement: We thank Sir Richard Roberts (NEB) for the kind gift of anti-4mC
  antibodies. We are also grateful to the JIC Small Molecule Mass Spectrometry (Lionel
  Hill) and Chemistry (Martin Rejzek) platforms as well as the High Resolution Metabolomics
  Laboratory (Manfred Beckmann, Aberystwyth University) for their assistance with
  LC-MS. Additionally, we acknowledge the assistance of the JIC Bioimaging Facility
  and ISTA Imaging and Optics Facility for microscopy. Finally, we appreciate the
  High Performance Computing resources provided by the ISTA Scientific Computing Facility
  and Norwich BioScience Institute Partnership Computing Infrastructure. This work
  was funded by a Sainsbury Charitable Foundation studentship (J.W.), a UKRI-BBSRC
  Doctoral Training Partnerships studentship (BBT0087171 to J.T.), a European Research
  Council Starting Grant (“SexMeth” 804981 to J.W., S.X., and X.F.), two Biotechnology
  and Biological Sciences Research Council (BBSRC) grants (BBS0096201 and BBP0135111
  to J.Z., M.V., and X.F.), an EMBO Long Term Fellowship (Y.L.), an ISTA Bridge Fellowship
  (S.X.), and ISTA core funding (Y.Y. and X.F.).
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: James
  full_name: Walker, James
  last_name: Walker
- first_name: Jingyi
  full_name: Zhang, Jingyi
  last_name: Zhang
- first_name: Yalin
  full_name: Liu, Yalin
  last_name: Liu
- first_name: Shujuan
  full_name: Xu, Shujuan
  id: 9724dd9d-f591-11ee-bd51-e97ed0652286
  last_name: Xu
- first_name: Yiming
  full_name: Yu, Yiming
  id: 318e643b-8b61-11ed-b69e-aafa103ec8dd
  last_name: Yu
  orcid: 0000-0002-9919-7282
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Weizhi
  full_name: Ouyang, Weizhi
  id: fec73395-8b60-11ed-b69e-927fda99c743
  last_name: Ouyang
- first_name: Judit
  full_name: Tálas, Judit
  last_name: Tálas
- first_name: Liam
  full_name: Dolan, Liam
  last_name: Dolan
- first_name: Keiji
  full_name: Nakajima, Keiji
  last_name: Nakajima
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Walker J, Zhang J, Liu Y, et al. Extensive N4 cytosine methylation is essential
    for Marchantia sperm function. <i>Cell</i>. 2025;188(11):2890-2906.e14. doi:<a
    href="https://doi.org/10.1016/j.cell.2025.03.014">10.1016/j.cell.2025.03.014</a>
  apa: Walker, J., Zhang, J., Liu, Y., Xu, S., Yu, Y., Vickers, M., … Feng, X. (2025).
    Extensive N4 cytosine methylation is essential for Marchantia sperm function.
    <i>Cell</i>. Elsevier. <a href="https://doi.org/10.1016/j.cell.2025.03.014">https://doi.org/10.1016/j.cell.2025.03.014</a>
  chicago: Walker, James, Jingyi Zhang, Yalin Liu, Shujuan Xu, Yiming Yu, Martin Vickers,
    Weizhi Ouyang, et al. “Extensive N4 Cytosine Methylation Is Essential for Marchantia
    Sperm Function.” <i>Cell</i>. Elsevier, 2025. <a href="https://doi.org/10.1016/j.cell.2025.03.014">https://doi.org/10.1016/j.cell.2025.03.014</a>.
  ieee: J. Walker <i>et al.</i>, “Extensive N4 cytosine methylation is essential for
    Marchantia sperm function,” <i>Cell</i>, vol. 188, no. 11. Elsevier, p. 2890–2906.e14,
    2025.
  ista: Walker J, Zhang J, Liu Y, Xu S, Yu Y, Vickers M, Ouyang W, Tálas J, Dolan
    L, Nakajima K, Feng X. 2025. Extensive N4 cytosine methylation is essential for
    Marchantia sperm function. Cell. 188(11), 2890–2906.e14.
  mla: Walker, James, et al. “Extensive N4 Cytosine Methylation Is Essential for Marchantia
    Sperm Function.” <i>Cell</i>, vol. 188, no. 11, Elsevier, 2025, p. 2890–2906.e14,
    doi:<a href="https://doi.org/10.1016/j.cell.2025.03.014">10.1016/j.cell.2025.03.014</a>.
  short: J. Walker, J. Zhang, Y. Liu, S. Xu, Y. Yu, M. Vickers, W. Ouyang, J. Tálas,
    L. Dolan, K. Nakajima, X. Feng, Cell 188 (2025) 2890–2906.e14.
corr_author: '1'
date_created: 2025-04-20T22:01:28Z
date_published: 2025-05-29T00:00:00Z
date_updated: 2026-04-28T13:36:51Z
day: '29'
ddc:
- '570'
department:
- _id: XiFe
doi: 10.1016/j.cell.2025.03.014
ec_funded: 1
external_id:
  isi:
  - '001504744800006'
  pmid:
  - '40209706'
file:
- access_level: open_access
  checksum: 0dcc2feb368dfe7c4890093366b2dacb
  content_type: application/pdf
  creator: dernst
  date_created: 2025-12-29T13:40:32Z
  date_updated: 2025-12-29T13:40:32Z
  file_id: '20871'
  file_name: 2025_Cell_Walker.pdf
  file_size: 11622960
  relation: main_file
  success: 1
file_date_updated: 2025-12-29T13:40:32Z
has_accepted_license: '1'
intvolume: '       188'
isi: 1
issue: '11'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 2890-2906.e14
pmid: 1
project:
- _id: bdb51a6e-d553-11ed-ba76-c2025f3d5725
  call_identifier: H2020
  grant_number: '804981'
  name: Establishment, modulation and inheritance of sexual lineage specific DNA methylation
    in plants
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  link:
  - description: News on ISTA website
    relation: press_release
    url: https://ista.ac.at/en/news/from-bacterial-immunity-to-plant-sex/
scopus_import: '1'
status: public
title: Extensive N4 cytosine methylation is essential for Marchantia sperm function
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: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 188
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '15375'
abstract:
- lang: eng
  text: In the eukaryotic nucleus, heterochromatin forms highly condensed, visible
    foci known as heterochromatin foci (HF). These HF are enriched with linker histone
    H1, a key player in heterochromatin condensation and silencing. However, it is
    unknown how H1 aggregates HF and condenses heterochromatin. In this study, we
    established that H1 facilitates heterochromatin condensation by enhancing inter-
    and intrachromosomal interactions between and within heterochromatic regions of
    the Arabidopsis (Arabidopsis thaliana) genome. We demonstrated that H1 drives
    HF formation via phase separation, which requires its C-terminal intrinsically
    disordered region (C-IDR). A truncated H1 lacking the C-IDR fails to form foci
    or recover HF in the h1 mutant background, whereas C-IDR with a short stretch
    of the globular domain (18 out of 71 amino acids) is sufficient to rescue both
    defects. In addition, C-IDR is essential for H1's roles in regulating nucleosome
    repeat length and DNA methylation in Arabidopsis, indicating that phase separation
    capability is required for chromatin functions of H1. Our data suggest that bacterial
    H1-like proteins, which have been shown to condense DNA, are intrinsically disordered
    and capable of mediating phase separation. Therefore, we propose that phase separation
    mediated by H1 or H1-like proteins may represent an ancient mechanism for condensing
    chromatin and DNA.
acknowledged_ssus:
- _id: Bio
- _id: ScienComp
acknowledgement: "This work was funded by ISTA core support (Y.Y. and X.F.) and grants
  from the National Natural Science Foundation of China (31871443 to L.W. and P.L.;
  32100417 to L.W.).\r\nWe thank the ISTA Imaging and Optics Facility for assistance
  with microscopy and the ISTA Scientific Computing Facility for high-performance
  computing resources."
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Yiming
  full_name: Yu, Yiming
  id: 318e643b-8b61-11ed-b69e-aafa103ec8dd
  last_name: Yu
- first_name: Liang
  full_name: Wang, Liang
  last_name: Wang
- first_name: Jingyi
  full_name: Zhang, Jingyi
  last_name: Zhang
- first_name: Zhengyong
  full_name: Bai, Zhengyong
  last_name: Bai
- first_name: Guohong
  full_name: Li, Guohong
  last_name: Li
- first_name: Pilong
  full_name: Li, Pilong
  last_name: Li
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: He S, Yu Y, Wang L, et al. Linker histone H1 drives heterochromatin condensation
    via phase separation in Arabidopsis. <i>The Plant Cell</i>. 2024;36(5):1829-1843.
    doi:<a href="https://doi.org/10.1093/plcell/koae034">10.1093/plcell/koae034</a>
  apa: He, S., Yu, Y., Wang, L., Zhang, J., Bai, Z., Li, G., … Feng, X. (2024). Linker
    histone H1 drives heterochromatin condensation via phase separation in Arabidopsis.
    <i>The Plant Cell</i>. Oxford University Press. <a href="https://doi.org/10.1093/plcell/koae034">https://doi.org/10.1093/plcell/koae034</a>
  chicago: He, Shengbo, Yiming Yu, Liang Wang, Jingyi Zhang, Zhengyong Bai, Guohong
    Li, Pilong Li, and Xiaoqi Feng. “Linker Histone H1 Drives Heterochromatin Condensation
    via Phase Separation in Arabidopsis.” <i>The Plant Cell</i>. Oxford University
    Press, 2024. <a href="https://doi.org/10.1093/plcell/koae034">https://doi.org/10.1093/plcell/koae034</a>.
  ieee: S. He <i>et al.</i>, “Linker histone H1 drives heterochromatin condensation
    via phase separation in Arabidopsis,” <i>The Plant Cell</i>, vol. 36, no. 5. Oxford
    University Press, pp. 1829–1843, 2024.
  ista: He S, Yu Y, Wang L, Zhang J, Bai Z, Li G, Li P, Feng X. 2024. Linker histone
    H1 drives heterochromatin condensation via phase separation in Arabidopsis. The
    Plant Cell. 36(5), 1829–1843.
  mla: He, Shengbo, et al. “Linker Histone H1 Drives Heterochromatin Condensation
    via Phase Separation in Arabidopsis.” <i>The Plant Cell</i>, vol. 36, no. 5, Oxford
    University Press, 2024, pp. 1829–43, doi:<a href="https://doi.org/10.1093/plcell/koae034">10.1093/plcell/koae034</a>.
  short: S. He, Y. Yu, L. Wang, J. Zhang, Z. Bai, G. Li, P. Li, X. Feng, The Plant
    Cell 36 (2024) 1829–1843.
corr_author: '1'
date_created: 2024-05-12T22:01:01Z
date_published: 2024-05-01T00:00:00Z
date_updated: 2025-09-08T07:21:17Z
day: '01'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.1093/plcell/koae034
external_id:
  isi:
  - '001180817000001'
  pmid:
  - '38309957'
file:
- access_level: open_access
  checksum: eed76c848fe3d8fe9a53943181aaa53c
  content_type: application/pdf
  creator: dernst
  date_created: 2025-04-23T07:43:12Z
  date_updated: 2025-04-23T07:43:12Z
  file_id: '19611'
  file_name: 2024_PlantCell_He.pdf
  file_size: 50791962
  relation: main_file
  success: 1
file_date_updated: 2025-04-23T07:43:12Z
has_accepted_license: '1'
intvolume: '        36'
isi: 1
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 1829-1843
pmid: 1
publication: The Plant Cell
publication_identifier:
  eissn:
  - 1532-298X
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Linker histone H1 drives heterochromatin condensation via phase separation
  in Arabidopsis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 36
year: '2024'
...
---
_id: '12668'
abstract:
- lang: eng
  text: "Background: Plant and animal embryogenesis have conserved and distinct features.
    Cell fate transitions occur during embryogenesis in both plants and animals. The
    epigenomic processes regulating plant embryogenesis remain largely elusive.\r\n\r\nResults:
    Here, we elucidate chromatin and transcriptomic dynamics during embryogenesis
    of the most cultivated crop, hexaploid wheat. Time-series analysis reveals stage-specific
    and proximal–distal distinct chromatin accessibility and dynamics concordant with
    transcriptome changes. Following fertilization, the remodeling kinetics of H3K4me3,
    H3K27ac, and H3K27me3 differ from that in mammals, highlighting considerable species-specific
    epigenomic dynamics during zygotic genome activation. Polycomb repressive complex
    2 (PRC2)-mediated H3K27me3 deposition is important for embryo establishment. Later
    H3K27ac, H3K27me3, and chromatin accessibility undergo dramatic remodeling to
    establish a permissive chromatin environment facilitating the access of transcription
    factors to cis-elements for fate patterning. Embryonic maturation is characterized
    by increasing H3K27me3 and decreasing chromatin accessibility, which likely participates
    in restricting totipotency while preventing extensive organogenesis. Finally,
    epigenomic signatures are correlated with biased expression among homeolog triads
    and divergent expression after polyploidization, revealing an epigenomic contributor
    to subgenome diversification in an allohexaploid genome.\r\n\r\nConclusions: Collectively,
    we present an invaluable resource for comparative and mechanistic analysis of
    the epigenomic regulation of crop embryogenesis."
article_number: '7'
article_processing_charge: No
article_type: original
author:
- first_name: Long
  full_name: Zhao, Long
  last_name: Zhao
- first_name: Yiman
  full_name: Yang, Yiman
  last_name: Yang
- first_name: Jinchao
  full_name: Chen, Jinchao
  last_name: Chen
- first_name: Xuelei
  full_name: Lin, Xuelei
  last_name: Lin
- first_name: Hao
  full_name: Zhang, Hao
  last_name: Zhang
- first_name: Hao
  full_name: Wang, Hao
  last_name: Wang
- first_name: Hongzhe
  full_name: Wang, Hongzhe
  last_name: Wang
- first_name: Xiaomin
  full_name: Bie, Xiaomin
  last_name: Bie
- first_name: Jiafu
  full_name: Jiang, Jiafu
  last_name: Jiang
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Xiangdong
  full_name: Fu, Xiangdong
  last_name: Fu
- first_name: Xiansheng
  full_name: Zhang, Xiansheng
  last_name: Zhang
- first_name: Zhuo
  full_name: Du, Zhuo
  last_name: Du
- first_name: Jun
  full_name: Xiao, Jun
  last_name: Xiao
citation:
  ama: Zhao L, Yang Y, Chen J, et al. Dynamic chromatin regulatory programs during
    embryogenesis of hexaploid wheat. <i>Genome Biology</i>. 2023;24. doi:<a href="https://doi.org/10.1186/s13059-022-02844-2">10.1186/s13059-022-02844-2</a>
  apa: Zhao, L., Yang, Y., Chen, J., Lin, X., Zhang, H., Wang, H., … Xiao, J. (2023).
    Dynamic chromatin regulatory programs during embryogenesis of hexaploid wheat.
    <i>Genome Biology</i>. Springer Nature. <a href="https://doi.org/10.1186/s13059-022-02844-2">https://doi.org/10.1186/s13059-022-02844-2</a>
  chicago: Zhao, Long, Yiman Yang, Jinchao Chen, Xuelei Lin, Hao Zhang, Hao Wang,
    Hongzhe Wang, et al. “Dynamic Chromatin Regulatory Programs during Embryogenesis
    of Hexaploid Wheat.” <i>Genome Biology</i>. Springer Nature, 2023. <a href="https://doi.org/10.1186/s13059-022-02844-2">https://doi.org/10.1186/s13059-022-02844-2</a>.
  ieee: L. Zhao <i>et al.</i>, “Dynamic chromatin regulatory programs during embryogenesis
    of hexaploid wheat,” <i>Genome Biology</i>, vol. 24. Springer Nature, 2023.
  ista: Zhao L, Yang Y, Chen J, Lin X, Zhang H, Wang H, Wang H, Bie X, Jiang J, Feng
    X, Fu X, Zhang X, Du Z, Xiao J. 2023. Dynamic chromatin regulatory programs during
    embryogenesis of hexaploid wheat. Genome Biology. 24, 7.
  mla: Zhao, Long, et al. “Dynamic Chromatin Regulatory Programs during Embryogenesis
    of Hexaploid Wheat.” <i>Genome Biology</i>, vol. 24, 7, Springer Nature, 2023,
    doi:<a href="https://doi.org/10.1186/s13059-022-02844-2">10.1186/s13059-022-02844-2</a>.
  short: L. Zhao, Y. Yang, J. Chen, X. Lin, H. Zhang, H. Wang, H. Wang, X. Bie, J.
    Jiang, X. Feng, X. Fu, X. Zhang, Z. Du, J. Xiao, Genome Biology 24 (2023).
date_created: 2023-02-23T09:13:49Z
date_published: 2023-01-13T00:00:00Z
date_updated: 2023-05-08T10:52:49Z
day: '13'
department:
- _id: XiFe
doi: 10.1186/s13059-022-02844-2
extern: '1'
external_id:
  pmid:
  - '36639687'
intvolume: '        24'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1186/s13059-022-02844-2
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Genome Biology
publication_identifier:
  issn:
  - 1474-760X
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic chromatin regulatory programs during embryogenesis of hexaploid wheat
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2023'
...
---
_id: '12669'
abstract:
- lang: eng
  text: The study of RNAs has become one of the most influential research fields in
    contemporary biology and biomedicine. In the last few years, new sequencing technologies
    have produced an explosion of new and exciting discoveries in the field but have
    also given rise to many open questions. Defining these questions, together with
    old, long-standing gaps in our knowledge, is the spirit of this article. The breadth
    of topics within RNA biology research is vast, and every aspect of the biology
    of these molecules contains countless exciting open questions. Here, we asked
    12 groups to discuss their most compelling question among some plant RNA biology
    topics. The following vignettes cover RNA alternative splicing; RNA dynamics;
    RNA translation; RNA structures; R-loops; epitranscriptomics; long non-coding
    RNAs; small RNA production and their functions in crops; small RNAs during gametogenesis
    and in cross-kingdom RNA interference; and RNA-directed DNA methylation. In each
    section, we will present the current state-of-the-art in plant RNA biology research
    before asking the questions that will surely motivate future discoveries in the
    field. We hope this article will spark a debate about the future perspective on
    RNA biology and provoke novel reflections in the reader.
article_number: koac346
article_processing_charge: No
article_type: original
author:
- first_name: Pablo A
  full_name: Manavella, Pablo A
  last_name: Manavella
- first_name: Micaela A
  full_name: Godoy Herz, Micaela A
  last_name: Godoy Herz
- first_name: Alberto R
  full_name: Kornblihtt, Alberto R
  last_name: Kornblihtt
- first_name: Reed
  full_name: Sorenson, Reed
  last_name: Sorenson
- first_name: Leslie E
  full_name: Sieburth, Leslie E
  last_name: Sieburth
- first_name: Kentaro
  full_name: Nakaminami, Kentaro
  last_name: Nakaminami
- first_name: Motoaki
  full_name: Seki, Motoaki
  last_name: Seki
- first_name: Yiliang
  full_name: Ding, Yiliang
  last_name: Ding
- first_name: Qianwen
  full_name: Sun, Qianwen
  last_name: Sun
- first_name: Hunseung
  full_name: Kang, Hunseung
  last_name: Kang
- first_name: Federico D
  full_name: Ariel, Federico D
  last_name: Ariel
- first_name: Martin
  full_name: Crespi, Martin
  last_name: Crespi
- first_name: Axel J
  full_name: Giudicatti, Axel J
  last_name: Giudicatti
- first_name: Qiang
  full_name: Cai, Qiang
  last_name: Cai
- first_name: Hailing
  full_name: Jin, Hailing
  last_name: Jin
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Yijun
  full_name: Qi, Yijun
  last_name: Qi
- first_name: Craig S
  full_name: Pikaard, Craig S
  last_name: Pikaard
citation:
  ama: 'Manavella PA, Godoy Herz MA, Kornblihtt AR, et al. Beyond transcription: compelling
    open questions in plant RNA biology. <i>The Plant Cell</i>. 2023;35(6). doi:<a
    href="https://doi.org/10.1093/plcell/koac346">10.1093/plcell/koac346</a>'
  apa: 'Manavella, P. A., Godoy Herz, M. A., Kornblihtt, A. R., Sorenson, R., Sieburth,
    L. E., Nakaminami, K., … Pikaard, C. S. (2023). Beyond transcription: compelling
    open questions in plant RNA biology. <i>The Plant Cell</i>. Oxford University
    Press. <a href="https://doi.org/10.1093/plcell/koac346">https://doi.org/10.1093/plcell/koac346</a>'
  chicago: 'Manavella, Pablo A, Micaela A Godoy Herz, Alberto R Kornblihtt, Reed Sorenson,
    Leslie E Sieburth, Kentaro Nakaminami, Motoaki Seki, et al. “Beyond Transcription:
    Compelling Open Questions in Plant RNA Biology.” <i>The Plant Cell</i>. Oxford
    University Press, 2023. <a href="https://doi.org/10.1093/plcell/koac346">https://doi.org/10.1093/plcell/koac346</a>.'
  ieee: 'P. A. Manavella <i>et al.</i>, “Beyond transcription: compelling open questions
    in plant RNA biology,” <i>The Plant Cell</i>, vol. 35, no. 6. Oxford University
    Press, 2023.'
  ista: 'Manavella PA, Godoy Herz MA, Kornblihtt AR, Sorenson R, Sieburth LE, Nakaminami
    K, Seki M, Ding Y, Sun Q, Kang H, Ariel FD, Crespi M, Giudicatti AJ, Cai Q, Jin
    H, Feng X, Qi Y, Pikaard CS. 2023. Beyond transcription: compelling open questions
    in plant RNA biology. The Plant Cell. 35(6), koac346.'
  mla: 'Manavella, Pablo A., et al. “Beyond Transcription: Compelling Open Questions
    in Plant RNA Biology.” <i>The Plant Cell</i>, vol. 35, no. 6, koac346, Oxford
    University Press, 2023, doi:<a href="https://doi.org/10.1093/plcell/koac346">10.1093/plcell/koac346</a>.'
  short: P.A. Manavella, M.A. Godoy Herz, A.R. Kornblihtt, R. Sorenson, L.E. Sieburth,
    K. Nakaminami, M. Seki, Y. Ding, Q. Sun, H. Kang, F.D. Ariel, M. Crespi, A.J.
    Giudicatti, Q. Cai, H. Jin, X. Feng, Y. Qi, C.S. Pikaard, The Plant Cell 35 (2023).
date_created: 2023-02-23T09:14:59Z
date_published: 2023-06-01T00:00:00Z
date_updated: 2023-10-04T09:48:43Z
day: '01'
department:
- _id: XiFe
doi: 10.1093/plcell/koac346
extern: '1'
external_id:
  pmid:
  - '36477566'
intvolume: '        35'
issue: '6'
keyword:
- Cell Biology
- Plant Science
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/plcell/koac346
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: The Plant Cell
publication_identifier:
  eissn:
  - 1532-298X
  issn:
  - 1040-4651
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Beyond transcription: compelling open questions in plant RNA biology'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 35
year: '2023'
...
---
_id: '12672'
abstract:
- lang: eng
  text: Cytosine methylation within CG dinucleotides (mCG) can be epigenetically inherited
    over many generations. Such inheritance is thought to be mediated by a semiconservative
    mechanism that produces binary present/absent methylation patterns. However, we
    show here that in Arabidopsis thaliana h1ddm1 mutants, intermediate heterochromatic
    mCG is stably inherited across many generations and is quantitatively associated
    with transposon expression. We develop a mathematical model that estimates the
    rates of semiconservative maintenance failure and de novo methylation at each
    transposon, demonstrating that mCG can be stably inherited at any level via a
    dynamic balance of these activities. We find that DRM2 – the core methyltransferase
    of the RNA-directed DNA methylation pathway – catalyzes most of the heterochromatic
    de novo mCG, with de novo rates orders of magnitude higher than previously thought,
    whereas chromomethylases make smaller contributions. Our results demonstrate that
    stable epigenetic inheritance of mCG in plant heterochromatin is enabled by extensive
    de novo methylation.
acknowledgement: The authors would like to thank Jasper Rine for advice and mentorship
  to D.B.L., Lesley Philips, Timothy Wells, Sophie Able, and Christina Wistrom for
  support with plant growth, and Bhagyshree Jamge and Frédéric Berger for help with
  analysis of ddm1 × WT RNA-sequencing data. This work was supported by BBSRC Institute
  Strategic Program GEN (BB/P013511/1) to X.F., M.H., and D.Z., a European Research
  Council grant MaintainMeth (725746) to D.Z., and a postdoctoral fellowship from
  the Helen Hay Whitney Foundation to D.B.L.
article_number: '112132'
article_processing_charge: Yes
article_type: original
author:
- first_name: David B.
  full_name: Lyons, David B.
  last_name: Lyons
- first_name: Amy
  full_name: Briffa, Amy
  last_name: Briffa
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Jaemyung
  full_name: Choi, Jaemyung
  last_name: Choi
- first_name: Elizabeth
  full_name: Hollwey, Elizabeth
  id: b8c4f54b-e484-11eb-8fdc-a54df64ef6dd
  last_name: Hollwey
- first_name: Jack
  full_name: Colicchio, Jack
  last_name: Colicchio
- first_name: Ian
  full_name: Anderson, Ian
  last_name: Anderson
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Martin
  full_name: Howard, Martin
  last_name: Howard
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Lyons DB, Briffa A, He S, et al. Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons. <i>Cell Reports</i>.
    2023;42(3). doi:<a href="https://doi.org/10.1016/j.celrep.2023.112132">10.1016/j.celrep.2023.112132</a>
  apa: Lyons, D. B., Briffa, A., He, S., Choi, J., Hollwey, E., Colicchio, J., … Zilberman,
    D. (2023). Extensive de novo activity stabilizes epigenetic inheritance of CG
    methylation in Arabidopsis transposons. <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.112132">https://doi.org/10.1016/j.celrep.2023.112132</a>
  chicago: Lyons, David B., Amy Briffa, Shengbo He, Jaemyung Choi, Elizabeth Hollwey,
    Jack Colicchio, Ian Anderson, Xiaoqi Feng, Martin Howard, and Daniel Zilberman.
    “Extensive de Novo Activity Stabilizes Epigenetic Inheritance of CG Methylation
    in Arabidopsis Transposons.” <i>Cell Reports</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.celrep.2023.112132">https://doi.org/10.1016/j.celrep.2023.112132</a>.
  ieee: D. B. Lyons <i>et al.</i>, “Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons,” <i>Cell Reports</i>,
    vol. 42, no. 3. Elsevier, 2023.
  ista: Lyons DB, Briffa A, He S, Choi J, Hollwey E, Colicchio J, Anderson I, Feng
    X, Howard M, Zilberman D. 2023. Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons. Cell Reports. 42(3),
    112132.
  mla: Lyons, David B., et al. “Extensive de Novo Activity Stabilizes Epigenetic Inheritance
    of CG Methylation in Arabidopsis Transposons.” <i>Cell Reports</i>, vol. 42, no.
    3, 112132, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.112132">10.1016/j.celrep.2023.112132</a>.
  short: D.B. Lyons, A. Briffa, S. He, J. Choi, E. Hollwey, J. Colicchio, I. Anderson,
    X. Feng, M. Howard, D. Zilberman, Cell Reports 42 (2023).
corr_author: '1'
date_created: 2023-02-23T09:17:44Z
date_published: 2023-03-28T00:00:00Z
date_updated: 2025-04-14T07:57:43Z
day: '28'
ddc:
- '580'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1016/j.celrep.2023.112132
ec_funded: 1
external_id:
  isi:
  - '000944921600001'
file:
- access_level: open_access
  checksum: 6cbc44fdb18bf18834c9e2a5b9c67123
  content_type: application/pdf
  creator: kschuh
  date_created: 2023-05-11T10:41:42Z
  date_updated: 2023-05-11T10:41:42Z
  file_id: '12941'
  file_name: 2023_CellReports_Lyons.pdf
  file_size: 8401261
  relation: main_file
  success: 1
file_date_updated: 2023-05-11T10:41:42Z
has_accepted_license: '1'
intvolume: '        42'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
project:
- _id: 62935a00-2b32-11ec-9570-eff30fa39068
  call_identifier: H2020
  grant_number: '725746'
  name: Quantitative analysis of DNA methylation maintenance with chromatin
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Extensive de novo activity stabilizes epigenetic inheritance of CG methylation
  in Arabidopsis transposons
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 42
year: '2023'
...
---
_id: '12670'
abstract:
- lang: eng
  text: DNA methylation plays essential homeostatic functions in eukaryotic genomes.
    In animals, DNA methylation is also developmentally regulated and, in turn, regulates
    development. In the past two decades, huge research effort has endorsed the understanding
    that DNA methylation plays a similar role in plant development, especially during
    sexual reproduction. The power of whole-genome sequencing and cell isolation techniques,
    as well as bioinformatics tools, have enabled recent studies to reveal dynamic
    changes in DNA methylation during germline development. Furthermore, the combination
    of these technological advances with genetics, developmental biology and cell
    biology tools has revealed functional methylation reprogramming events that control
    gene and transposon activities in flowering plant germlines. In this review, we
    discuss the major advances in our knowledge of DNA methylation dynamics during
    male and female germline development in flowering plants.
article_processing_charge: No
article_type: review
author:
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: He S, Feng X. DNA methylation dynamics during germline development. <i>Journal
    of Integrative Plant Biology</i>. 2022;64(12):2240-2251. doi:<a href="https://doi.org/10.1111/jipb.13422">10.1111/jipb.13422</a>
  apa: He, S., &#38; Feng, X. (2022). DNA methylation dynamics during germline development.
    <i>Journal of Integrative Plant Biology</i>. Wiley. <a href="https://doi.org/10.1111/jipb.13422">https://doi.org/10.1111/jipb.13422</a>
  chicago: He, Shengbo, and Xiaoqi Feng. “DNA Methylation Dynamics during Germline
    Development.” <i>Journal of Integrative Plant Biology</i>. Wiley, 2022. <a href="https://doi.org/10.1111/jipb.13422">https://doi.org/10.1111/jipb.13422</a>.
  ieee: S. He and X. Feng, “DNA methylation dynamics during germline development,”
    <i>Journal of Integrative Plant Biology</i>, vol. 64, no. 12. Wiley, pp. 2240–2251,
    2022.
  ista: He S, Feng X. 2022. DNA methylation dynamics during germline development.
    Journal of Integrative Plant Biology. 64(12), 2240–2251.
  mla: He, Shengbo, and Xiaoqi Feng. “DNA Methylation Dynamics during Germline Development.”
    <i>Journal of Integrative Plant Biology</i>, vol. 64, no. 12, Wiley, 2022, pp.
    2240–51, doi:<a href="https://doi.org/10.1111/jipb.13422">10.1111/jipb.13422</a>.
  short: S. He, X. Feng, Journal of Integrative Plant Biology 64 (2022) 2240–2251.
date_created: 2023-02-23T09:15:57Z
date_published: 2022-12-07T00:00:00Z
date_updated: 2024-10-14T12:03:14Z
day: '07'
department:
- _id: XiFe
doi: 10.1111/jipb.13422
extern: '1'
external_id:
  pmid:
  - '36478632'
intvolume: '        64'
issue: '12'
keyword:
- Plant Science
- General Biochemistry
- Genetics and Molecular Biology
- Biochemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1111/jipb.13422
month: '12'
oa: 1
oa_version: Published Version
page: 2240-2251
pmid: 1
publication: Journal of Integrative Plant Biology
publication_identifier:
  eissn:
  - 1744-7909
  issn:
  - 1672-9072
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA methylation dynamics during germline development
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 64
year: '2022'
...
---
_id: '12671'
abstract:
- lang: eng
  text: Sperm chromatin is typically transformed by protamines into a compact and
    transcriptionally inactive state1,2. Sperm cells of flowering plants lack protamines,
    yet they have small, transcriptionally active nuclei with chromatin condensed
    through an unknown mechanism3,4. Here we show that a histone variant, H2B.8, mediates
    sperm chromatin and nuclear condensation in Arabidopsis thaliana. Loss of H2B.8
    causes enlarged sperm nuclei with dispersed chromatin, whereas ectopic expression
    in somatic cells produces smaller nuclei with aggregated chromatin. This result
    demonstrates that H2B.8 is sufficient for chromatin condensation. H2B.8 aggregates
    transcriptionally inactive AT-rich chromatin into phase-separated condensates,
    which facilitates nuclear compaction without reducing transcription. Reciprocal
    crosses show that mutation of h2b.8 reduces male transmission, which suggests
    that H2B.8-mediated sperm compaction is important for fertility. Altogether, our
    results reveal a new mechanism of nuclear compaction through global aggregation
    of unexpressed chromatin. We propose that H2B.8 is an evolutionary innovation
    of flowering plants that achieves nuclear condensation compatible with active
    transcription.
article_processing_charge: No
article_type: original
author:
- first_name: Toby
  full_name: Buttress, Toby
  last_name: Buttress
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Liang
  full_name: Wang, Liang
  last_name: Wang
- first_name: Shaoli
  full_name: Zhou, Shaoli
  last_name: Zhou
- first_name: Gerhard
  full_name: Saalbach, Gerhard
  last_name: Saalbach
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Guohong
  full_name: Li, Guohong
  last_name: Li
- first_name: Pilong
  full_name: Li, Pilong
  last_name: Li
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Buttress T, He S, Wang L, et al. Histone H2B.8 compacts flowering plant sperm
    through chromatin phase separation. <i>Nature</i>. 2022;611(7936):614-622. doi:<a
    href="https://doi.org/10.1038/s41586-022-05386-6">10.1038/s41586-022-05386-6</a>
  apa: Buttress, T., He, S., Wang, L., Zhou, S., Saalbach, G., Vickers, M., … Feng,
    X. (2022). Histone H2B.8 compacts flowering plant sperm through chromatin phase
    separation. <i>Nature</i>. Springer Nature. <a href="https://doi.org/10.1038/s41586-022-05386-6">https://doi.org/10.1038/s41586-022-05386-6</a>
  chicago: Buttress, Toby, Shengbo He, Liang Wang, Shaoli Zhou, Gerhard Saalbach,
    Martin Vickers, Guohong Li, Pilong Li, and Xiaoqi Feng. “Histone H2B.8 Compacts
    Flowering Plant Sperm through Chromatin Phase Separation.” <i>Nature</i>. Springer
    Nature, 2022. <a href="https://doi.org/10.1038/s41586-022-05386-6">https://doi.org/10.1038/s41586-022-05386-6</a>.
  ieee: T. Buttress <i>et al.</i>, “Histone H2B.8 compacts flowering plant sperm through
    chromatin phase separation,” <i>Nature</i>, vol. 611, no. 7936. Springer Nature,
    pp. 614–622, 2022.
  ista: Buttress T, He S, Wang L, Zhou S, Saalbach G, Vickers M, Li G, Li P, Feng
    X. 2022. Histone H2B.8 compacts flowering plant sperm through chromatin phase
    separation. Nature. 611(7936), 614–622.
  mla: Buttress, Toby, et al. “Histone H2B.8 Compacts Flowering Plant Sperm through
    Chromatin Phase Separation.” <i>Nature</i>, vol. 611, no. 7936, Springer Nature,
    2022, pp. 614–22, doi:<a href="https://doi.org/10.1038/s41586-022-05386-6">10.1038/s41586-022-05386-6</a>.
  short: T. Buttress, S. He, L. Wang, S. Zhou, G. Saalbach, M. Vickers, G. Li, P.
    Li, X. Feng, Nature 611 (2022) 614–622.
date_created: 2023-02-23T09:17:05Z
date_published: 2022-11-17T00:00:00Z
date_updated: 2024-10-14T12:03:36Z
day: '17'
department:
- _id: XiFe
doi: 10.1038/s41586-022-05386-6
extern: '1'
external_id:
  pmid:
  - '36323776'
intvolume: '       611'
issue: '7936'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1038/s41586-022-05386-6
month: '11'
oa: 1
oa_version: Published Version
page: 614-622
pmid: 1
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Histone H2B.8 compacts flowering plant sperm through chromatin phase separation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 611
year: '2022'
...
---
_id: '12186'
abstract:
- lang: eng
  text: Activation of cell-surface and intracellular receptor-mediated immunity results
    in rapid transcriptional reprogramming that underpins disease resistance. However,
    the mechanisms by which co-activation of both immune systems lead to transcriptional
    changes are not clear. Here, we combine RNA-seq and ATAC-seq to define changes
    in gene expression and chromatin accessibility. Activation of cell-surface or
    intracellular receptor-mediated immunity, or both, increases chromatin accessibility
    at induced defence genes. Analysis of ATAC-seq and RNA-seq data combined with
    publicly available information on transcription factor DNA-binding motifs enabled
    comparison of individual gene regulatory networks activated by cell-surface or
    intracellular receptor-mediated immunity, or by both. These results and analyses
    reveal overlapping and conserved transcriptional regulatory mechanisms between
    the two immune systems.
acknowledgement: "We thank the Gatsby Foundation (UK) for funding to the JDGJ laboratory.
  PD acknowledges support from the European Union’s Horizon 2020 Research and Innovation
  Program under Marie Skłodowska Curie Actions (grant agreement: 656243) and a Future
  Leader Fellowship from the Biotechnology and Biological Sciences Research Council
  (BBSRC) (grant agreement: BB/R012172/1). TS, RKS, DM, and JDGJ were supported by
  the Gatsby Foundation funding to the\r\nSainsbury Laboratory. NMP and KV were supported
  by a BOF grant from Ghent University (grant agreement: BOF24Y2019001901). WG and
  RZ were supported by the Scottish Government Rural and Environment Science and Analytical
  Services division (RESAS), and RZ also acknowledges the support from a BBSRC Bioinformatics
  and Biological Resources Fund (grant agreement: BB/S020160/1).BPMN was supported
  by the Norwich Research Park (NRP) Biosciences Doctoral Training Partnership (DTP)
  funded by the BBSRC (grant agreement: BB/M011216/1). SH and XF were supported by
  a BBSRC Responsive Mode grant (grant agreement: BB/S009620/1) and a European Research
  Council Starting grant ‘SexMeth’ (grant agreement: 804981). CL was supported by
  Deutsche Forschungsgemeinschaft (grant agreement: LI 2862/4). "
article_processing_charge: No
article_type: original
author:
- first_name: Pingtao
  full_name: Ding, Pingtao
  last_name: Ding
- first_name: Toshiyuki
  full_name: Sakai, Toshiyuki
  last_name: Sakai
- first_name: Ram
  full_name: Krishna Shrestha, Ram
  last_name: Krishna Shrestha
- first_name: Nicolas
  full_name: Manosalva Perez, Nicolas
  last_name: Manosalva Perez
- first_name: Wenbin
  full_name: Guo, Wenbin
  last_name: Guo
- first_name: Bruno Pok Man
  full_name: Ngou, Bruno Pok Man
  last_name: Ngou
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Chang
  full_name: Liu, Chang
  last_name: Liu
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Runxuan
  full_name: Zhang, Runxuan
  last_name: Zhang
- first_name: Klaas
  full_name: Vandepoele, Klaas
  last_name: Vandepoele
- first_name: Dan
  full_name: MacLean, Dan
  last_name: MacLean
- first_name: Jonathan D G
  full_name: Jones, Jonathan D G
  last_name: Jones
citation:
  ama: Ding P, Sakai T, Krishna Shrestha R, et al. Chromatin accessibility landscapes
    activated by cell-surface and intracellular immune receptors. <i>Journal of Experimental
    Botany</i>. 2021;72(22):7927-7941. doi:<a href="https://doi.org/10.1093/jxb/erab373">10.1093/jxb/erab373</a>
  apa: Ding, P., Sakai, T., Krishna Shrestha, R., Manosalva Perez, N., Guo, W., Ngou,
    B. P. M., … Jones, J. D. G. (2021). Chromatin accessibility landscapes activated
    by cell-surface and intracellular immune receptors. <i>Journal of Experimental
    Botany</i>. Oxford University Press. <a href="https://doi.org/10.1093/jxb/erab373">https://doi.org/10.1093/jxb/erab373</a>
  chicago: Ding, Pingtao, Toshiyuki Sakai, Ram Krishna Shrestha, Nicolas Manosalva
    Perez, Wenbin Guo, Bruno Pok Man Ngou, Shengbo He, et al. “Chromatin Accessibility
    Landscapes Activated by Cell-Surface and Intracellular Immune Receptors.” <i>Journal
    of Experimental Botany</i>. Oxford University Press, 2021. <a href="https://doi.org/10.1093/jxb/erab373">https://doi.org/10.1093/jxb/erab373</a>.
  ieee: P. Ding <i>et al.</i>, “Chromatin accessibility landscapes activated by cell-surface
    and intracellular immune receptors,” <i>Journal of Experimental Botany</i>, vol.
    72, no. 22. Oxford University Press, pp. 7927–7941, 2021.
  ista: Ding P, Sakai T, Krishna Shrestha R, Manosalva Perez N, Guo W, Ngou BPM, He
    S, Liu C, Feng X, Zhang R, Vandepoele K, MacLean D, Jones JDG. 2021. Chromatin
    accessibility landscapes activated by cell-surface and intracellular immune receptors.
    Journal of Experimental Botany. 72(22), 7927–7941.
  mla: Ding, Pingtao, et al. “Chromatin Accessibility Landscapes Activated by Cell-Surface
    and Intracellular Immune Receptors.” <i>Journal of Experimental Botany</i>, vol.
    72, no. 22, Oxford University Press, 2021, pp. 7927–41, doi:<a href="https://doi.org/10.1093/jxb/erab373">10.1093/jxb/erab373</a>.
  short: P. Ding, T. Sakai, R. Krishna Shrestha, N. Manosalva Perez, W. Guo, B.P.M.
    Ngou, S. He, C. Liu, X. Feng, R. Zhang, K. Vandepoele, D. MacLean, J.D.G. Jones,
    Journal of Experimental Botany 72 (2021) 7927–7941.
date_created: 2023-01-16T09:14:35Z
date_published: 2021-08-13T00:00:00Z
date_updated: 2023-05-08T11:01:18Z
day: '13'
department:
- _id: XiFe
doi: 10.1093/jxb/erab373
extern: '1'
external_id:
  pmid:
  - '34387350'
intvolume: '        72'
issue: '22'
keyword:
- Plant Science
- Physiology
language:
- iso: eng
month: '08'
oa_version: None
page: 7927-7941
pmid: 1
publication: Journal of Experimental Botany
publication_identifier:
  issn:
  - 0022-0957
  - 1460-2431
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Chromatin accessibility landscapes activated by cell-surface and intracellular
  immune receptors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 72
year: '2021'
...
---
OA_place: repository
OA_type: green
_id: '12187'
abstract:
- lang: eng
  text: Genomes of germ cells present an existential vulnerability to organisms because
    germ cell mutations will propagate to future generations. Transposable elements
    are one source of such mutations. In the small flowering plant Arabidopsis, Long
    et al. found that genome methylation in the male germline is directed by small
    interfering RNAs (siRNAs) imperfectly transcribed from transposons (see the Perspective
    by Mosher). These germline siRNAs silence germline transposons and establish inherited
    methylation patterns in sperm, thus maintaining the integrity of the plant genome
    across generations.
acknowledgement: 'We thank the John Innes Centre Bioimaging Facility (S. Lopez, E.
  Wegel, and K. Findlay) for their assistance with microscopy and the Norwich BioScience
  Institute Partnership Computing Infrastructure for Science Group for high-performance
  computing resources. Funding: This work was funded by a European Research Council
  Starting Grant (“SexMeth” 804981; J.L., J.W., and X.F.), a Sainsbury Charitable
  Foundation studentship (J.W.), two Biotechnology and Biological Sciences Research
  Council (BBSRC) grants (BBS0096201 and BBP0135111; W.S., M.V., and X.F.), two John
  Innes Foundation studentships (B.A. and S.D.), and a BBSRC David Phillips Fellowship
  (BBL0250431; H.G. and X.F.). Author contributions: J.L., J.W., and X.F. designed
  the study and wrote the manuscript; J.L., W.S., B.A., H.G., and S.D. performed the
  experiments; and J.L., J.W., B.A., H.G., S.D., M.V., and X.F. analyzed the data.
  Competing interests: The authors declare no competing interests. Data and material
  availability: All sequencing data have been deposited in the Gene Expression Omnibus
  (GEO) under accession no. GSE161625. Accession nos. of published datasets used in
  this study are listed in table S6. Published software used in this study include
  Bowtie v1.2.2 (https://doi.org/10.1002/0471250953.bi1107s32), Bismark v0.22.2 (https://doi.org/10.1093/bioinformatics/btr167),
  Kallisto v0.43.0 (https://doi.org/10.1038/nbt0816-888d), Shortstack v3.8.5 (https://doi.org/10.1534/g3.116.030452),
  and Cutadapt v1.15 (https://doi.org/10.1089/cmb.2017.0096). TrimGalore v0.4.1 and
  MarkDuplicates v1.141 are available from https://github.com/FelixKrueger/TrimGalore
  and https://github.com/broadinstitute/picard, respectively. All remaining data are
  in the main paper or the supplementary materials.'
article_processing_charge: No
article_type: original
author:
- first_name: Jincheng
  full_name: Long, Jincheng
  last_name: Long
- first_name: James
  full_name: Walker, James
  last_name: Walker
- first_name: Wenjing
  full_name: She, Wenjing
  last_name: She
- first_name: Billy
  full_name: Aldridge, Billy
  last_name: Aldridge
- first_name: Hongbo
  full_name: Gao, Hongbo
  last_name: Gao
- first_name: Samuel
  full_name: Deans, Samuel
  last_name: Deans
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Long J, Walker J, She W, et al. Nurse cell-derived small RNAs define paternal
    epigenetic inheritance in Arabidopsis. <i>Science</i>. 2021;373(6550). doi:<a
    href="https://doi.org/10.1126/science.abh0556">10.1126/science.abh0556</a>
  apa: Long, J., Walker, J., She, W., Aldridge, B., Gao, H., Deans, S., … Feng, X.
    (2021). Nurse cell-derived small RNAs define paternal epigenetic inheritance in
    Arabidopsis. <i>Science</i>. American Association for the Advancement of Science.
    <a href="https://doi.org/10.1126/science.abh0556">https://doi.org/10.1126/science.abh0556</a>
  chicago: Long, Jincheng, James Walker, Wenjing She, Billy Aldridge, Hongbo Gao,
    Samuel Deans, Martin Vickers, and Xiaoqi Feng. “Nurse Cell-Derived Small RNAs
    Define Paternal Epigenetic Inheritance in Arabidopsis.” <i>Science</i>. American
    Association for the Advancement of Science, 2021. <a href="https://doi.org/10.1126/science.abh0556">https://doi.org/10.1126/science.abh0556</a>.
  ieee: J. Long <i>et al.</i>, “Nurse cell-derived small RNAs define paternal epigenetic
    inheritance in Arabidopsis,” <i>Science</i>, vol. 373, no. 6550. American Association
    for the Advancement of Science, 2021.
  ista: Long J, Walker J, She W, Aldridge B, Gao H, Deans S, Vickers M, Feng X. 2021.
    Nurse cell-derived small RNAs define paternal epigenetic inheritance in Arabidopsis.
    Science. 373(6550).
  mla: Long, Jincheng, et al. “Nurse Cell-Derived Small RNAs Define Paternal Epigenetic
    Inheritance in Arabidopsis.” <i>Science</i>, vol. 373, no. 6550, American Association
    for the Advancement of Science, 2021, doi:<a href="https://doi.org/10.1126/science.abh0556">10.1126/science.abh0556</a>.
  short: J. Long, J. Walker, W. She, B. Aldridge, H. Gao, S. Deans, M. Vickers, X.
    Feng, Science 373 (2021).
date_created: 2023-01-16T09:15:14Z
date_published: 2021-07-02T00:00:00Z
date_updated: 2026-03-19T10:52:21Z
day: '02'
department:
- _id: XiFe
doi: 10.1126/science.abh0556
extern: '1'
external_id:
  pmid:
  - '34210850'
intvolume: '       373'
issue: '6550'
keyword:
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2021.01.25.428150
month: '07'
oa: 1
oa_version: Preprint
pmid: 1
publication: Science
publication_identifier:
  eissn:
  - 1095-9203
  issn:
  - 0036-8075
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nurse cell-derived small RNAs define paternal epigenetic inheritance in Arabidopsis
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 373
year: '2021'
...
---
_id: '12188'
abstract:
- lang: eng
  text: Molecular mechanisms enabling the switching and maintenance of epigenetic
    states are not fully understood. Distinct histone modifications are often associated
    with ON/OFF epigenetic states, but how these states are stably maintained through
    DNA replication, yet in certain situations switch from one to another remains
    unclear. Here, we address this problem through identification of Arabidopsis INCURVATA11
    (ICU11) as a Polycomb Repressive Complex 2 accessory protein. ICU11 robustly immunoprecipitated
    in vivo with PRC2 core components and the accessory proteins, EMBRYONIC FLOWER
    1 (EMF1), LIKE HETEROCHROMATIN PROTEIN1 (LHP1), and TELOMERE_REPEAT_BINDING FACTORS
    (TRBs). ICU11 encodes a 2-oxoglutarate-dependent dioxygenase, an activity associated
    with histone demethylation in other organisms, and mutant plants show defects
    in multiple aspects of the Arabidopsis epigenome. To investigate its primary molecular
    function we identified the Arabidopsis FLOWERING LOCUS C (FLC) as a direct target
    and found icu11 disrupted the cold-induced, Polycomb-mediated silencing underlying
    vernalization. icu11 prevented reduction in H3K36me3 levels normally seen during
    the early cold phase, supporting a role for ICU11 in H3K36me3 demethylation. This
    was coincident with an attenuation of H3K27me3 at the internal nucleation site
    in FLC, and reduction in H3K27me3 levels across the body of the gene after plants
    were returned to the warm. Thus, ICU11 is required for the cold-induced epigenetic
    switching between the mutually exclusive chromatin states at FLC, from the active
    H3K36me3 state to the silenced H3K27me3 state. These data support the importance
    of physical coupling of histone modification activities to promote epigenetic
    switching between opposing chromatin states.
acknowledgement: We would like to thank Scott Berry for help with ICU-GFP nuclear
  localization microscopy, Hao Yu and Lisha Shen for assistance with 6mA DNA methylation
  analysis, Donna Gibson for graphic design assistance, and members of the C.D. and
  Howard laboratories for helpful discussions. This work was funded by the European
  Research Council grants to “MEXTIM” (to C.D.) and “SexMeth” (to X. Feng), by the
  Biotechnological and Biological Sciences Research Council (BBSRC) Institute Strategic
  Programmes GRO (BB/J004588/1), GEN (BB/P013511/1), BBSRC grant (to X. Feng) (BB/S009620/1),
  and the Marie Sklodowska–Curie Postdoctoral Fellowships “UNRAVEL” (to R.H.B.) and
  "WISDOM" (to X. Fang). Additional funding via the Wellcome Trust through a Senior
  Research Fellowship (to J.R.) (103139) and a multiuser equipment grant (108504).
  The Wellcome Centre for Cell Biology is supported by core funding from the Wellcome
  Trust (203149).
article_processing_charge: No
article_type: original
author:
- first_name: Rebecca H.
  full_name: Bloomer, Rebecca H.
  last_name: Bloomer
- first_name: Claire E.
  full_name: Hutchison, Claire E.
  last_name: Hutchison
- first_name: Isabel
  full_name: Bäurle, Isabel
  last_name: Bäurle
- first_name: James
  full_name: Walker, James
  last_name: Walker
- first_name: Xiaofeng
  full_name: Fang, Xiaofeng
  last_name: Fang
- first_name: Pumi
  full_name: Perera, Pumi
  last_name: Perera
- first_name: Christos N.
  full_name: Velanis, Christos N.
  last_name: Velanis
- first_name: Serin
  full_name: Gümüs, Serin
  last_name: Gümüs
- first_name: Christos
  full_name: Spanos, Christos
  last_name: Spanos
- first_name: Juri
  full_name: Rappsilber, Juri
  last_name: Rappsilber
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Justin
  full_name: Goodrich, Justin
  last_name: Goodrich
- first_name: Caroline
  full_name: Dean, Caroline
  last_name: Dean
citation:
  ama: Bloomer RH, Hutchison CE, Bäurle I, et al. The  Arabidopsis epigenetic regulator
    ICU11 as an accessory protein of polycomb repressive complex 2. <i>Proceedings
    of the National Academy of Sciences</i>. 2020;117(28):16660-16666. doi:<a href="https://doi.org/10.1073/pnas.1920621117">10.1073/pnas.1920621117</a>
  apa: Bloomer, R. H., Hutchison, C. E., Bäurle, I., Walker, J., Fang, X., Perera,
    P., … Dean, C. (2020). The  Arabidopsis epigenetic regulator ICU11 as an accessory
    protein of polycomb repressive complex 2. <i>Proceedings of the National Academy
    of Sciences</i>. Proceedings of the National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1920621117">https://doi.org/10.1073/pnas.1920621117</a>
  chicago: Bloomer, Rebecca H., Claire E. Hutchison, Isabel Bäurle, James Walker,
    Xiaofeng Fang, Pumi Perera, Christos N. Velanis, et al. “The  Arabidopsis Epigenetic
    Regulator ICU11 as an Accessory Protein of Polycomb Repressive Complex 2.” <i>Proceedings
    of the National Academy of Sciences</i>. Proceedings of the National Academy of
    Sciences, 2020. <a href="https://doi.org/10.1073/pnas.1920621117">https://doi.org/10.1073/pnas.1920621117</a>.
  ieee: R. H. Bloomer <i>et al.</i>, “The  Arabidopsis epigenetic regulator ICU11
    as an accessory protein of polycomb repressive complex 2,” <i>Proceedings of the
    National Academy of Sciences</i>, vol. 117, no. 28. Proceedings of the National
    Academy of Sciences, pp. 16660–16666, 2020.
  ista: Bloomer RH, Hutchison CE, Bäurle I, Walker J, Fang X, Perera P, Velanis CN,
    Gümüs S, Spanos C, Rappsilber J, Feng X, Goodrich J, Dean C. 2020. The  Arabidopsis
    epigenetic regulator ICU11 as an accessory protein of polycomb repressive complex
    2. Proceedings of the National Academy of Sciences. 117(28), 16660–16666.
  mla: Bloomer, Rebecca H., et al. “The  Arabidopsis Epigenetic Regulator ICU11 as
    an Accessory Protein of Polycomb Repressive Complex 2.” <i>Proceedings of the
    National Academy of Sciences</i>, vol. 117, no. 28, Proceedings of the National
    Academy of Sciences, 2020, pp. 16660–66, doi:<a href="https://doi.org/10.1073/pnas.1920621117">10.1073/pnas.1920621117</a>.
  short: R.H. Bloomer, C.E. Hutchison, I. Bäurle, J. Walker, X. Fang, P. Perera, C.N.
    Velanis, S. Gümüs, C. Spanos, J. Rappsilber, X. Feng, J. Goodrich, C. Dean, Proceedings
    of the National Academy of Sciences 117 (2020) 16660–16666.
date_created: 2023-01-16T09:15:44Z
date_published: 2020-05-22T00:00:00Z
date_updated: 2023-05-08T10:53:55Z
day: '22'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.1073/pnas.1920621117
extern: '1'
external_id:
  pmid:
  - '32601198'
file:
- access_level: open_access
  checksum: cedee184cb12f454f2fba4158ff47db9
  content_type: application/pdf
  creator: alisjak
  date_created: 2023-02-07T11:29:55Z
  date_updated: 2023-02-07T11:29:55Z
  file_id: '12526'
  file_name: 2020_PNAS_Bloomer.pdf
  file_size: 1105414
  relation: main_file
  success: 1
file_date_updated: 2023-02-07T11:29:55Z
has_accepted_license: '1'
intvolume: '       117'
issue: '28'
keyword:
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368280/
month: '05'
oa: 1
oa_version: Published Version
page: 16660-16666
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  issn:
  - 0027-8424
  - 1091-6490
publication_status: published
publisher: Proceedings of the National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: The  Arabidopsis epigenetic regulator ICU11 as an accessory protein of polycomb
  repressive complex 2
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: 117
year: '2020'
...
---
_id: '12189'
abstract:
- lang: eng
  text: Meiotic crossovers (COs) are important for reshuffling genetic information
    between homologous chromosomes and they are essential for their correct segregation.
    COs are unevenly distributed along chromosomes and the underlying mechanisms controlling
    CO localization are not well understood. We previously showed that meiotic COs
    are mis-localized in the absence of AXR1, an enzyme involved in the neddylation/rubylation
    protein modification pathway in Arabidopsis thaliana. Here, we report that in
    axr1-/-, male meiocytes show a strong defect in chromosome pairing whereas the
    formation of the telomere bouquet is not affected. COs are also redistributed
    towards subtelomeric chromosomal ends where they frequently form clusters, in
    contrast to large central regions depleted in recombination. The CO suppressed
    regions correlate with DNA hypermethylation of transposable elements (TEs) in
    the CHH context in axr1-/- meiocytes. Through examining somatic methylomes, we
    found axr1-/- affects DNA methylation in a plant, causing hypermethylation in
    all sequence contexts (CG, CHG and CHH) in TEs. Impairment of the main pathways
    involved in DNA methylation is epistatic over axr1-/- for DNA methylation in somatic
    cells but does not restore regular chromosome segregation during meiosis. Collectively,
    our findings reveal that the neddylation pathway not only regulates hormonal perception
    and CO distribution but is also, directly or indirectly, a major limiting pathway
    of TE DNA methylation in somatic cells.
acknowledgement: The authors wish to thank Cécile Raynaud, Eric Jenczewski, Rajeev
  Kumar, Raphaël Mercier and Jean Molinier for critical reading of the manuscript.
article_number: e1008894
article_processing_charge: No
article_type: original
author:
- first_name: Nicolas
  full_name: Christophorou, Nicolas
  last_name: Christophorou
- first_name: Wenjing
  full_name: She, Wenjing
  last_name: She
- first_name: Jincheng
  full_name: Long, Jincheng
  last_name: Long
- first_name: Aurélie
  full_name: Hurel, Aurélie
  last_name: Hurel
- first_name: Sébastien
  full_name: Beaubiat, Sébastien
  last_name: Beaubiat
- first_name: Yassir
  full_name: Idir, Yassir
  last_name: Idir
- first_name: Marina
  full_name: Tagliaro-Jahns, Marina
  last_name: Tagliaro-Jahns
- first_name: Aurélie
  full_name: Chambon, Aurélie
  last_name: Chambon
- first_name: Victor
  full_name: Solier, Victor
  last_name: Solier
- first_name: Daniel
  full_name: Vezon, Daniel
  last_name: Vezon
- first_name: Mathilde
  full_name: Grelon, Mathilde
  last_name: Grelon
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Nicolas
  full_name: Bouché, Nicolas
  last_name: Bouché
- first_name: Christine
  full_name: Mézard, Christine
  last_name: Mézard
citation:
  ama: Christophorou N, She W, Long J, et al. AXR1 affects DNA methylation independently
    of its role in regulating meiotic crossover localization. <i>PLOS Genetics</i>.
    2020;16(6). doi:<a href="https://doi.org/10.1371/journal.pgen.1008894">10.1371/journal.pgen.1008894</a>
  apa: Christophorou, N., She, W., Long, J., Hurel, A., Beaubiat, S., Idir, Y., …
    Mézard, C. (2020). AXR1 affects DNA methylation independently of its role in regulating
    meiotic crossover localization. <i>PLOS Genetics</i>. Public Library of Science
    (PLoS). <a href="https://doi.org/10.1371/journal.pgen.1008894">https://doi.org/10.1371/journal.pgen.1008894</a>
  chicago: Christophorou, Nicolas, Wenjing She, Jincheng Long, Aurélie Hurel, Sébastien
    Beaubiat, Yassir Idir, Marina Tagliaro-Jahns, et al. “AXR1 Affects DNA Methylation
    Independently of Its Role in Regulating Meiotic Crossover Localization.” <i>PLOS
    Genetics</i>. Public Library of Science (PLoS), 2020. <a href="https://doi.org/10.1371/journal.pgen.1008894">https://doi.org/10.1371/journal.pgen.1008894</a>.
  ieee: N. Christophorou <i>et al.</i>, “AXR1 affects DNA methylation independently
    of its role in regulating meiotic crossover localization,” <i>PLOS Genetics</i>,
    vol. 16, no. 6. Public Library of Science (PLoS), 2020.
  ista: Christophorou N, She W, Long J, Hurel A, Beaubiat S, Idir Y, Tagliaro-Jahns
    M, Chambon A, Solier V, Vezon D, Grelon M, Feng X, Bouché N, Mézard C. 2020. AXR1
    affects DNA methylation independently of its role in regulating meiotic crossover
    localization. PLOS Genetics. 16(6), e1008894.
  mla: Christophorou, Nicolas, et al. “AXR1 Affects DNA Methylation Independently
    of Its Role in Regulating Meiotic Crossover Localization.” <i>PLOS Genetics</i>,
    vol. 16, no. 6, e1008894, Public Library of Science (PLoS), 2020, doi:<a href="https://doi.org/10.1371/journal.pgen.1008894">10.1371/journal.pgen.1008894</a>.
  short: N. Christophorou, W. She, J. Long, A. Hurel, S. Beaubiat, Y. Idir, M. Tagliaro-Jahns,
    A. Chambon, V. Solier, D. Vezon, M. Grelon, X. Feng, N. Bouché, C. Mézard, PLOS
    Genetics 16 (2020).
date_created: 2023-01-16T09:16:10Z
date_published: 2020-06-29T00:00:00Z
date_updated: 2023-05-08T10:54:39Z
day: '29'
department:
- _id: XiFe
doi: 10.1371/journal.pgen.1008894
extern: '1'
external_id:
  pmid:
  - '32598340'
intvolume: '        16'
issue: '6'
keyword:
- Cancer Research
- Genetics (clinical)
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351236/
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLOS Genetics
publication_identifier:
  issn:
  - 1553-7404
publication_status: published
publisher: Public Library of Science (PLoS)
quality_controlled: '1'
scopus_import: '1'
status: public
title: AXR1 affects DNA methylation independently of its role in regulating meiotic
  crossover localization
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2020'
...
---
_id: '12190'
abstract:
- lang: eng
  text: Meiotic crossover frequency varies within genomes, which influences genetic
    diversity and adaptation. In turn, genetic variation within populations can act
    to modify crossover frequency in cis and trans. To identify genetic variation
    that controls meiotic crossover frequency, we screened Arabidopsis accessions
    using fluorescent recombination reporters. We mapped a genetic modifier of crossover
    frequency in Col × Bur populations of Arabidopsis to a premature stop codon within
    TBP-ASSOCIATED FACTOR 4b (TAF4b), which encodes a subunit of the RNA polymerase
    II general transcription factor TFIID. The Arabidopsis taf4b mutation is a rare
    variant found in the British Isles, originating in South-West Ireland. Using genetics,
    genomics, and immunocytology, we demonstrate a genome-wide decrease in taf4b crossovers,
    with strongest reduction in the sub-telomeric regions. Using RNA sequencing (RNA-seq)
    from purified meiocytes, we show that TAF4b expression is meiocyte enriched, whereas
    its paralog TAF4 is broadly expressed. Consistent with the role of TFIID in promoting
    gene expression, RNA-seq of wild-type and taf4b meiocytes identified widespread
    transcriptional changes, including in genes that regulate the meiotic cell cycle
    and recombination. Therefore, TAF4b duplication is associated with acquisition
    of meiocyte-specific expression and promotion of germline transcription, which
    act directly or indirectly to elevate crossovers. This identifies a novel mode
    of meiotic recombination control via a general transcription factor.
acknowledgement: "We thank Gregory Copenhaver (University of North Carolina), Avraham
  Levy (The Weizmann Institute), and Scott Poethig (University of Pennsylvania) for
  FTLs; Piotr Ziolkowski for Col-420/Bur seed; Sureshkumar Balasubramanian\r\n(Monash
  University) for providing British and Irish Arabidopsis accessions; Mathilde Grelon
  (INRA, Versailles) for providing the MLH1 antibody; and the Gurdon Institute for
  access to microscopes. This work was supported by a BBSRC DTP studentship (E.J.L.),
  European Research Area Network for Coordinating Action in Plant Sciences/BBSRC ‘‘DeCOP’’
  (BB/M004937/1; C.L.), a BBSRC David Phillips Fellowship (BB/L025043/1; H.G. and
  X.F.), the European Research Council (CoG ‘‘SynthHotspot,’’ A.J.T., C.L., and I.R.H.;
  StG ‘‘SexMeth,’’ X.F.), and a Sainsbury Charitable Foundation Studentship (A.R.B.)."
article_processing_charge: No
article_type: original
author:
- first_name: Emma J.
  full_name: Lawrence, Emma J.
  last_name: Lawrence
- first_name: Hongbo
  full_name: Gao, Hongbo
  last_name: Gao
- first_name: Andrew J.
  full_name: Tock, Andrew J.
  last_name: Tock
- first_name: Christophe
  full_name: Lambing, Christophe
  last_name: Lambing
- first_name: Alexander R.
  full_name: Blackwell, Alexander R.
  last_name: Blackwell
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Ian R.
  full_name: Henderson, Ian R.
  last_name: Henderson
citation:
  ama: Lawrence EJ, Gao H, Tock AJ, et al. Natural variation in TBP-ASSOCIATED FACTOR
    4b controls meiotic crossover and germline transcription in Arabidopsis. <i>Current
    Biology</i>. 2019;29(16):2676-2686.e3. doi:<a href="https://doi.org/10.1016/j.cub.2019.06.084">10.1016/j.cub.2019.06.084</a>
  apa: Lawrence, E. J., Gao, H., Tock, A. J., Lambing, C., Blackwell, A. R., Feng,
    X., &#38; Henderson, I. R. (2019). Natural variation in TBP-ASSOCIATED FACTOR
    4b controls meiotic crossover and germline transcription in Arabidopsis. <i>Current
    Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.cub.2019.06.084">https://doi.org/10.1016/j.cub.2019.06.084</a>
  chicago: Lawrence, Emma J., Hongbo Gao, Andrew J. Tock, Christophe Lambing, Alexander
    R. Blackwell, Xiaoqi Feng, and Ian R. Henderson. “Natural Variation in TBP-ASSOCIATED
    FACTOR 4b Controls Meiotic Crossover and Germline Transcription in Arabidopsis.”
    <i>Current Biology</i>. Elsevier, 2019. <a href="https://doi.org/10.1016/j.cub.2019.06.084">https://doi.org/10.1016/j.cub.2019.06.084</a>.
  ieee: E. J. Lawrence <i>et al.</i>, “Natural variation in TBP-ASSOCIATED FACTOR
    4b controls meiotic crossover and germline transcription in Arabidopsis,” <i>Current
    Biology</i>, vol. 29, no. 16. Elsevier, p. 2676–2686.e3, 2019.
  ista: Lawrence EJ, Gao H, Tock AJ, Lambing C, Blackwell AR, Feng X, Henderson IR.
    2019. Natural variation in TBP-ASSOCIATED FACTOR 4b controls meiotic crossover
    and germline transcription in Arabidopsis. Current Biology. 29(16), 2676–2686.e3.
  mla: Lawrence, Emma J., et al. “Natural Variation in TBP-ASSOCIATED FACTOR 4b Controls
    Meiotic Crossover and Germline Transcription in Arabidopsis.” <i>Current Biology</i>,
    vol. 29, no. 16, Elsevier, 2019, p. 2676–2686.e3, doi:<a href="https://doi.org/10.1016/j.cub.2019.06.084">10.1016/j.cub.2019.06.084</a>.
  short: E.J. Lawrence, H. Gao, A.J. Tock, C. Lambing, A.R. Blackwell, X. Feng, I.R.
    Henderson, Current Biology 29 (2019) 2676–2686.e3.
date_created: 2023-01-16T09:16:33Z
date_published: 2019-08-19T00:00:00Z
date_updated: 2025-01-14T14:31:02Z
day: '19'
department:
- _id: XiFe
doi: 10.1016/j.cub.2019.06.084
extern: '1'
external_id:
  pmid:
  - '31378616'
intvolume: '        29'
issue: '16'
keyword:
- General Agricultural and Biological Sciences
- General Biochemistry
- Genetics and Molecular Biology
language:
- iso: eng
month: '08'
oa_version: None
page: 2676-2686.e3
pmid: 1
publication: Current Biology
publication_identifier:
  issn:
  - 0960-9822
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Natural variation in TBP-ASSOCIATED FACTOR 4b controls meiotic crossover and
  germline transcription in Arabidopsis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 29
year: '2019'
...
---
_id: '12192'
abstract:
- lang: eng
  text: Transposable elements (TEs), the movement of which can damage the genome,
    are epigenetically silenced in eukaryotes. Intriguingly, TEs are activated in
    the sperm companion cell – vegetative cell (VC) – of the flowering plant Arabidopsis
    thaliana. However, the extent and mechanism of this activation are unknown. Here
    we show that about 100 heterochromatic TEs are activated in VCs, mostly by DEMETER-catalyzed
    DNA demethylation. We further demonstrate that DEMETER access to some of these
    TEs is permitted by the natural depletion of linker histone H1 in VCs. Ectopically
    expressed H1 suppresses TEs in VCs by reducing DNA demethylation and via a methylation-independent
    mechanism. We demonstrate that H1 is required for heterochromatin condensation
    in plant cells and show that H1 overexpression creates heterochromatic foci in
    the VC progenitor cell. Taken together, our results demonstrate that the natural
    depletion of H1 during male gametogenesis facilitates DEMETER-directed DNA demethylation,
    heterochromatin relaxation, and TE activation.
acknowledgement: We thank David Twell for the pDONR-P4-P1R-pLAT52 and pDONR-P2R-P3-mRFP
  vectors, the John Innes Centre Bioimaging Facility (Elaine Barclay and Grant Calder)
  for their assistance with microscopy, and the Norwich BioScience Institute Partnership
  Computing infrastructure for Science Group for High Performance Computing resources.
  This work was funded by a Biotechnology and Biological Sciences Research Council
  (BBSRC) David Phillips Fellowship (BB/L025043/1; SH, JZ and XF), a European Research
  Council Starting Grant ('SexMeth' 804981; XF) and a Grant to Exceptional Researchers
  by the Gatsby Charitable Foundation (SH and XF).
article_number: '42530'
article_processing_charge: No
article_type: original
author:
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Jingyi
  full_name: Zhang, Jingyi
  last_name: Zhang
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: He S, Vickers M, Zhang J, Feng X. Natural depletion of histone H1 in sex cells
    causes DNA demethylation, heterochromatin decondensation and transposon activation.
    <i>eLife</i>. 2019;8. doi:<a href="https://doi.org/10.7554/elife.42530">10.7554/elife.42530</a>
  apa: He, S., Vickers, M., Zhang, J., &#38; Feng, X. (2019). Natural depletion of
    histone H1 in sex cells causes DNA demethylation, heterochromatin decondensation
    and transposon activation. <i>ELife</i>. eLife Sciences Publications. <a href="https://doi.org/10.7554/elife.42530">https://doi.org/10.7554/elife.42530</a>
  chicago: He, Shengbo, Martin Vickers, Jingyi Zhang, and Xiaoqi Feng. “Natural Depletion
    of Histone H1 in Sex Cells Causes DNA Demethylation, Heterochromatin Decondensation
    and Transposon Activation.” <i>ELife</i>. eLife Sciences Publications, 2019. <a
    href="https://doi.org/10.7554/elife.42530">https://doi.org/10.7554/elife.42530</a>.
  ieee: S. He, M. Vickers, J. Zhang, and X. Feng, “Natural depletion of histone H1
    in sex cells causes DNA demethylation, heterochromatin decondensation and transposon
    activation,” <i>eLife</i>, vol. 8. eLife Sciences Publications, 2019.
  ista: He S, Vickers M, Zhang J, Feng X. 2019. Natural depletion of histone H1 in
    sex cells causes DNA demethylation, heterochromatin decondensation and transposon
    activation. eLife. 8, 42530.
  mla: He, Shengbo, et al. “Natural Depletion of Histone H1 in Sex Cells Causes DNA
    Demethylation, Heterochromatin Decondensation and Transposon Activation.” <i>ELife</i>,
    vol. 8, 42530, eLife Sciences Publications, 2019, doi:<a href="https://doi.org/10.7554/elife.42530">10.7554/elife.42530</a>.
  short: S. He, M. Vickers, J. Zhang, X. Feng, ELife 8 (2019).
date_created: 2023-01-16T09:17:21Z
date_published: 2019-05-28T00:00:00Z
date_updated: 2025-01-14T14:31:41Z
day: '28'
ddc:
- '580'
department:
- _id: XiFe
doi: 10.7554/elife.42530
extern: '1'
external_id:
  unknown:
  - '31135340'
file:
- access_level: open_access
  checksum: ea6b89c20d59e5eb3646916fe5d568ad
  content_type: application/pdf
  creator: alisjak
  date_created: 2023-02-07T09:42:46Z
  date_updated: 2023-02-07T09:42:46Z
  file_id: '12525'
  file_name: 2019_elife_He.pdf
  file_size: 2493837
  relation: main_file
  success: 1
file_date_updated: 2023-02-07T09:42:46Z
has_accepted_license: '1'
intvolume: '         8'
keyword:
- General Immunology and Microbiology
- General Biochemistry
- Genetics and Molecular Biology
- General Medicine
- General Neuroscience
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
publication: eLife
publication_identifier:
  issn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Natural depletion of histone H1 in sex cells causes DNA demethylation, heterochromatin
  decondensation and transposon activation
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2019'
...
---
OA_place: repository
OA_type: green
_id: '12193'
abstract:
- lang: eng
  text: DNA methylation regulates eukaryotic gene expression and is extensively reprogrammed
    during animal development. However, whether developmental methylation reprogramming
    during the sporophytic life cycle of flowering plants regulates genes is presently
    unknown. Here we report a distinctive gene-targeted RNA-directed DNA methylation
    (RdDM) activity in the Arabidopsis thaliana male sexual lineage that regulates
    gene expression in meiocytes. Loss of sexual-lineage-specific RdDM causes mis-splicing
    of the MPS1 gene (also known as PRD2), thereby disrupting meiosis. Our results
    establish a regulatory paradigm in which de novo methylation creates a cell-lineage-specific
    epigenetic signature that controls gene expression and contributes to cellular
    function in flowering plants.
acknowledgement: We thank Daniel Zilberman for intellectual contributions to this
  work and assistance with manuscript preparation. We also thank Caroline Dean, Kirsten
  Bomblies, Vinod Kumar, Siobhan Brady and Sophien Kamoun for comments on the manuscript,
  Hugh Dickinson and Josephine Hellberg for developing the meiocyte isolation method,
  Giles Oldroyd for the pGWB13-Bar vector, Elisa Fiume for the pMDC107-NTF vector,
  Matthew Hartley, Matthew Couchman and Tjelvar Sten Gunnar Olsson for bioinformatics
  support, and the John Innes Centre Bioimaging Facility (Elaine Barclay and Grant
  Calder) for their assistance with microscopy. This work was funded by a Biotechnology
  and Biological Sciences Research Council (BBSRC) David Phillips Fellowship (BBL0250431)
  to X.F., a BBSRC grant (BBM01973X1) to J.H., and a Sainsbury PhD Studentship to
  J.W.
article_processing_charge: No
article_type: original
author:
- first_name: James
  full_name: Walker, James
  last_name: Walker
- first_name: Hongbo
  full_name: Gao, Hongbo
  last_name: Gao
- first_name: Jingyi
  full_name: Zhang, Jingyi
  last_name: Zhang
- first_name: Billy
  full_name: Aldridge, Billy
  last_name: Aldridge
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: James D.
  full_name: Higgins, James D.
  last_name: Higgins
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Walker J, Gao H, Zhang J, et al. Sexual-lineage-specific DNA methylation regulates
    meiosis in Arabidopsis. <i>Nature Genetics</i>. 2017;50(1):130-137. doi:<a href="https://doi.org/10.1038/s41588-017-0008-5">10.1038/s41588-017-0008-5</a>
  apa: Walker, J., Gao, H., Zhang, J., Aldridge, B., Vickers, M., Higgins, J. D.,
    &#38; Feng, X. (2017). Sexual-lineage-specific DNA methylation regulates meiosis
    in Arabidopsis. <i>Nature Genetics</i>. Nature Research. <a href="https://doi.org/10.1038/s41588-017-0008-5">https://doi.org/10.1038/s41588-017-0008-5</a>
  chicago: Walker, James, Hongbo Gao, Jingyi Zhang, Billy Aldridge, Martin Vickers,
    James D. Higgins, and Xiaoqi Feng. “Sexual-Lineage-Specific DNA Methylation Regulates
    Meiosis in Arabidopsis.” <i>Nature Genetics</i>. Nature Research, 2017. <a href="https://doi.org/10.1038/s41588-017-0008-5">https://doi.org/10.1038/s41588-017-0008-5</a>.
  ieee: J. Walker <i>et al.</i>, “Sexual-lineage-specific DNA methylation regulates
    meiosis in Arabidopsis,” <i>Nature Genetics</i>, vol. 50, no. 1. Nature Research,
    pp. 130–137, 2017.
  ista: Walker J, Gao H, Zhang J, Aldridge B, Vickers M, Higgins JD, Feng X. 2017.
    Sexual-lineage-specific DNA methylation regulates meiosis in Arabidopsis. Nature
    Genetics. 50(1), 130–137.
  mla: Walker, James, et al. “Sexual-Lineage-Specific DNA Methylation Regulates Meiosis
    in Arabidopsis.” <i>Nature Genetics</i>, vol. 50, no. 1, Nature Research, 2017,
    pp. 130–37, doi:<a href="https://doi.org/10.1038/s41588-017-0008-5">10.1038/s41588-017-0008-5</a>.
  short: J. Walker, H. Gao, J. Zhang, B. Aldridge, M. Vickers, J.D. Higgins, X. Feng,
    Nature Genetics 50 (2017) 130–137.
date_created: 2023-01-16T09:18:05Z
date_published: 2017-12-18T00:00:00Z
date_updated: 2026-03-19T10:51:18Z
day: '18'
department:
- _id: XiFe
doi: 10.1038/s41588-017-0008-5
extern: '1'
external_id:
  pmid:
  - '29255257'
intvolume: '        50'
issue: '1'
keyword:
- Genetics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611288/
month: '12'
oa: 1
oa_version: Submitted Version
page: 130-137
pmid: 1
publication: Nature Genetics
publication_identifier:
  eissn:
  - 1546-1718
  issn:
  - 1061-4036
publication_status: published
publisher: Nature Research
quality_controlled: '1'
scopus_import: '1'
status: public
title: Sexual-lineage-specific DNA methylation regulates meiosis in Arabidopsis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 50
year: '2017'
...
---
_id: '9473'
abstract:
- lang: eng
  text: Cytosine DNA methylation regulates the expression of eukaryotic genes and
    transposons. Methylation is copied by methyltransferases after DNA replication,
    which results in faithful transmission of methylation patterns during cell division
    and, at least in flowering plants, across generations. Transgenerational inheritance
    is mediated by a small group of cells that includes gametes and their progenitors.
    However, methylation is usually analyzed in somatic tissues that do not contribute
    to the next generation, and the mechanisms of transgenerational inheritance are
    inferred from such studies. To gain a better understanding of how DNA methylation
    is inherited, we analyzed purified Arabidopsis thaliana sperm and vegetative cells-the
    cell types that comprise pollen-with mutations in the DRM, CMT2, and CMT3 methyltransferases.
    We find that DNA methylation dependency on these enzymes is similar in sperm,
    vegetative cells, and somatic tissues, although DRM activity extends into heterochromatin
    in vegetative cells, likely reflecting transcription of heterochromatic transposons
    in this cell type. We also show that lack of histone H1, which elevates heterochromatic
    DNA methylation in somatic tissues, does not have this effect in pollen. Instead,
    levels of CG methylation in wild-type sperm and vegetative cells, as well as in
    wild-type microspores from which both pollen cell types originate, are substantially
    higher than in wild-type somatic tissues and similar to those of H1-depleted roots.
    Our results demonstrate that the mechanisms of methylation maintenance are similar
    between pollen and somatic cells, but the efficiency of CG methylation is higher
    in pollen, allowing methylation patterns to be accurately inherited across generations.
article_processing_charge: No
article_type: original
author:
- first_name: Ping-Hung
  full_name: Hsieh, Ping-Hung
  last_name: Hsieh
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Toby
  full_name: Buttress, Toby
  last_name: Buttress
- first_name: Hongbo
  full_name: Gao, Hongbo
  last_name: Gao
- first_name: Matthew
  full_name: Couchman, Matthew
  last_name: Couchman
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Hsieh P-H, He S, Buttress T, et al. Arabidopsis male sexual lineage exhibits
    more robust maintenance of CG methylation than somatic tissues. <i>Proceedings
    of the National Academy of Sciences</i>. 2016;113(52):15132-15137. doi:<a href="https://doi.org/10.1073/pnas.1619074114">10.1073/pnas.1619074114</a>
  apa: Hsieh, P.-H., He, S., Buttress, T., Gao, H., Couchman, M., Fischer, R. L.,
    … Feng, X. (2016). Arabidopsis male sexual lineage exhibits more robust maintenance
    of CG methylation than somatic tissues. <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1619074114">https://doi.org/10.1073/pnas.1619074114</a>
  chicago: Hsieh, Ping-Hung, Shengbo He, Toby Buttress, Hongbo Gao, Matthew Couchman,
    Robert L. Fischer, Daniel Zilberman, and Xiaoqi Feng. “Arabidopsis Male Sexual
    Lineage Exhibits More Robust Maintenance of CG Methylation than Somatic Tissues.”
    <i>Proceedings of the National Academy of Sciences</i>. National Academy of Sciences,
    2016. <a href="https://doi.org/10.1073/pnas.1619074114">https://doi.org/10.1073/pnas.1619074114</a>.
  ieee: P.-H. Hsieh <i>et al.</i>, “Arabidopsis male sexual lineage exhibits more
    robust maintenance of CG methylation than somatic tissues,” <i>Proceedings of
    the National Academy of Sciences</i>, vol. 113, no. 52. National Academy of Sciences,
    pp. 15132–15137, 2016.
  ista: Hsieh P-H, He S, Buttress T, Gao H, Couchman M, Fischer RL, Zilberman D, Feng
    X. 2016. Arabidopsis male sexual lineage exhibits more robust maintenance of CG
    methylation than somatic tissues. Proceedings of the National Academy of Sciences.
    113(52), 15132–15137.
  mla: Hsieh, Ping-Hung, et al. “Arabidopsis Male Sexual Lineage Exhibits More Robust
    Maintenance of CG Methylation than Somatic Tissues.” <i>Proceedings of the National
    Academy of Sciences</i>, vol. 113, no. 52, National Academy of Sciences, 2016,
    pp. 15132–37, doi:<a href="https://doi.org/10.1073/pnas.1619074114">10.1073/pnas.1619074114</a>.
  short: P.-H. Hsieh, S. He, T. Buttress, H. Gao, M. Couchman, R.L. Fischer, D. Zilberman,
    X. Feng, Proceedings of the National Academy of Sciences 113 (2016) 15132–15137.
date_created: 2021-06-07T06:21:39Z
date_published: 2016-12-27T00:00:00Z
date_updated: 2023-05-08T11:00:40Z
day: '27'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1073/pnas.1619074114
extern: '1'
external_id:
  pmid:
  - '27956643'
intvolume: '       113'
issue: '52'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1619074114
month: '12'
oa: 1
oa_version: Published Version
page: 15132-15137
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arabidopsis male sexual lineage exhibits more robust maintenance of CG methylation
  than somatic tissues
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 113
year: '2016'
...
---
_id: '9477'
abstract:
- lang: eng
  text: Cytosine methylation is a DNA modification with important regulatory functions
    in eukaryotes. In flowering plants, sexual reproduction is accompanied by extensive
    DNA demethylation, which is required for proper gene expression in the endosperm,
    a nutritive extraembryonic seed tissue. Endosperm arises from a fusion of a sperm
    cell carried in the pollen and a female central cell. Endosperm DNA demethylation
    is observed specifically on the chromosomes inherited from the central cell in
    Arabidopsis thaliana, rice, and maize, and requires the DEMETER DNA demethylase
    in Arabidopsis. DEMETER is expressed in the central cell before fertilization,
    suggesting that endosperm demethylation patterns are inherited from the central
    cell. Down-regulation of the MET1 DNA methyltransferase has also been proposed
    to contribute to central cell demethylation. However, with the exception of three
    maize genes, central cell DNA methylation has not been directly measured, leaving
    the origin and mechanism of endosperm demethylation uncertain. Here, we report
    genome-wide analysis of DNA methylation in the central cells of Arabidopsis and
    rice—species that diverged 150 million years ago—as well as in rice egg cells.
    We find that DNA demethylation in both species is initiated in central cells,
    which requires DEMETER in Arabidopsis. However, we do not observe a global reduction
    of CG methylation that would be indicative of lowered MET1 activity; on the contrary,
    CG methylation efficiency is elevated in female gametes compared with nonsexual
    tissues. Our results demonstrate that locus-specific, active DNA demethylation
    in the central cell is the origin of maternal chromosome hypomethylation in the
    endosperm.
article_processing_charge: No
article_type: original
author:
- first_name: Kyunghyuk
  full_name: Park, Kyunghyuk
  last_name: Park
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Jin-Sup
  full_name: Park, Jin-Sup
  last_name: Park
- first_name: Youbong
  full_name: Hyun, Youbong
  last_name: Hyun
- first_name: Takashi
  full_name: Okamoto, Takashi
  last_name: Okamoto
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Yeonhee
  full_name: Choi, Yeonhee
  last_name: Choi
- first_name: Stefan
  full_name: Scholten, Stefan
  last_name: Scholten
citation:
  ama: Park K, Kim MY, Vickers M, et al. DNA demethylation is initiated in the central
    cells of Arabidopsis and rice. <i>Proceedings of the National Academy of Sciences</i>.
    2016;113(52):15138-15143. doi:<a href="https://doi.org/10.1073/pnas.1619047114">10.1073/pnas.1619047114</a>
  apa: Park, K., Kim, M. Y., Vickers, M., Park, J.-S., Hyun, Y., Okamoto, T., … Scholten,
    S. (2016). DNA demethylation is initiated in the central cells of Arabidopsis
    and rice. <i>Proceedings of the National Academy of Sciences</i>. National Academy
    of Sciences. <a href="https://doi.org/10.1073/pnas.1619047114">https://doi.org/10.1073/pnas.1619047114</a>
  chicago: Park, Kyunghyuk, M. Yvonne Kim, Martin Vickers, Jin-Sup Park, Youbong Hyun,
    Takashi Okamoto, Daniel Zilberman, et al. “DNA Demethylation Is Initiated in the
    Central Cells of Arabidopsis and Rice.” <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences, 2016. <a href="https://doi.org/10.1073/pnas.1619047114">https://doi.org/10.1073/pnas.1619047114</a>.
  ieee: K. Park <i>et al.</i>, “DNA demethylation is initiated in the central cells
    of Arabidopsis and rice,” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 113, no. 52. National Academy of Sciences, pp. 15138–15143, 2016.
  ista: Park K, Kim MY, Vickers M, Park J-S, Hyun Y, Okamoto T, Zilberman D, Fischer
    RL, Feng X, Choi Y, Scholten S. 2016. DNA demethylation is initiated in the central
    cells of Arabidopsis and rice. Proceedings of the National Academy of Sciences.
    113(52), 15138–15143.
  mla: Park, Kyunghyuk, et al. “DNA Demethylation Is Initiated in the Central Cells
    of Arabidopsis and Rice.” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 113, no. 52, National Academy of Sciences, 2016, pp. 15138–43, doi:<a href="https://doi.org/10.1073/pnas.1619047114">10.1073/pnas.1619047114</a>.
  short: K. Park, M.Y. Kim, M. Vickers, J.-S. Park, Y. Hyun, T. Okamoto, D. Zilberman,
    R.L. Fischer, X. Feng, Y. Choi, S. Scholten, Proceedings of the National Academy
    of Sciences 113 (2016) 15138–15143.
date_created: 2021-06-07T07:10:59Z
date_published: 2016-12-27T00:00:00Z
date_updated: 2023-05-08T11:00:07Z
day: '27'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1073/pnas.1619047114
extern: '1'
external_id:
  pmid:
  - '27956642'
intvolume: '       113'
issue: '52'
keyword:
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1619047114
month: '12'
oa: 1
oa_version: Published Version
page: 15138-15143
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA demethylation is initiated in the central cells of Arabidopsis and rice
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 113
year: '2016'
...
---
_id: '12196'
abstract:
- lang: eng
  text: SNC1 (SUPPRESSOR OF NPR1, CONSTITUTIVE 1) is one of a suite of intracellular
    Arabidopsis NOD-like receptor (NLR) proteins which, upon activation, result in
    the induction of defense responses. However, the molecular mechanisms underlying
    NLR activation and the subsequent provocation of immune responses are only partially
    characterized. To identify negative regulators of NLR-mediated immunity, a forward
    genetic screen was undertaken to search for enhancers of the dwarf, autoimmune
    gain-of-function snc1 mutant. To avoid lethality resulting from severe dwarfism,
    the screen was conducted using mos4 (modifier of snc1, 4) snc1 plants, which display
    wild-type-like morphology and resistance. M2 progeny were screened for mutant,
    snc1-enhancing (muse) mutants displaying a reversion to snc1-like phenotypes.
    The muse9 mos4 snc1 triple mutant was found to exhibit dwarf morphology, elevated
    expression of the pPR2-GUS defense marker reporter gene and enhanced resistance
    to the oomycete pathogen Hyaloperonospora arabidopsidis Noco2. Via map-based cloning
    and Illumina sequencing, it was determined that the muse9 mutation is in the gene
    encoding the SWI/SNF chromatin remodeler SYD (SPLAYED), and was thus renamed syd-10.
    The syd-10 single mutant has no observable alteration from wild-type-like resistance,
    although the syd-4 T-DNA insertion allele displays enhanced resistance to the
    bacterial pathogen Pseudomonas syringae pv. maculicola ES4326. Transcription of
    SNC1 is increased in both syd-4 and syd-10. These data suggest that SYD plays
    a subtle, specific role in the regulation of SNC1 expression and SNC1-mediated
    immunity. SYD may work with other proteins at the chromatin level to repress SNC1
    transcription; such regulation is important for fine-tuning the expression of
    NLR-encoding genes to prevent unpropitious autoimmunity.
acknowledgement: "This work was supported by the National Sciences and Engineering
  Research Council of Canada [Canada Graduate\r\nScholarship–Doctoral to K.J.; Discovery
  Grant to X.L.]; the department of Botany at the University of f British Columbia\r\n[the
  Dewar Cooper Memorial Fund to X.L.].The authors would like to thank Dr. Yuelin Zhang
  and Ms. Yan Li for their assistance with next-generation sequencing, and Mr. Charles
  Copeland for critical reading of the manuscript."
article_processing_charge: No
article_type: original
author:
- first_name: Kaeli C.M.
  full_name: Johnson, Kaeli C.M.
  last_name: Johnson
- first_name: Shitou
  full_name: Xia, Shitou
  last_name: Xia
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Xin
  full_name: Li, Xin
  last_name: Li
citation:
  ama: Johnson KCM, Xia S, Feng X, Li X. The chromatin remodeler SPLAYED negatively
    regulates SNC1-mediated immunity. <i>Plant and Cell Physiology</i>. 2015;56(8):1616-1623.
    doi:<a href="https://doi.org/10.1093/pcp/pcv087">10.1093/pcp/pcv087</a>
  apa: Johnson, K. C. M., Xia, S., Feng, X., &#38; Li, X. (2015). The chromatin remodeler
    SPLAYED negatively regulates SNC1-mediated immunity. <i>Plant and Cell Physiology</i>.
    Oxford University Press. <a href="https://doi.org/10.1093/pcp/pcv087">https://doi.org/10.1093/pcp/pcv087</a>
  chicago: Johnson, Kaeli C.M., Shitou Xia, Xiaoqi Feng, and Xin Li. “The Chromatin
    Remodeler SPLAYED Negatively Regulates SNC1-Mediated Immunity.” <i>Plant and Cell
    Physiology</i>. Oxford University Press, 2015. <a href="https://doi.org/10.1093/pcp/pcv087">https://doi.org/10.1093/pcp/pcv087</a>.
  ieee: K. C. M. Johnson, S. Xia, X. Feng, and X. Li, “The chromatin remodeler SPLAYED
    negatively regulates SNC1-mediated immunity,” <i>Plant and Cell Physiology</i>,
    vol. 56, no. 8. Oxford University Press, pp. 1616–1623, 2015.
  ista: Johnson KCM, Xia S, Feng X, Li X. 2015. The chromatin remodeler SPLAYED negatively
    regulates SNC1-mediated immunity. Plant and Cell Physiology. 56(8), 1616–1623.
  mla: Johnson, Kaeli C. M., et al. “The Chromatin Remodeler SPLAYED Negatively Regulates
    SNC1-Mediated Immunity.” <i>Plant and Cell Physiology</i>, vol. 56, no. 8, Oxford
    University Press, 2015, pp. 1616–23, doi:<a href="https://doi.org/10.1093/pcp/pcv087">10.1093/pcp/pcv087</a>.
  short: K.C.M. Johnson, S. Xia, X. Feng, X. Li, Plant and Cell Physiology 56 (2015)
    1616–1623.
date_created: 2023-01-16T09:20:22Z
date_published: 2015-08-01T00:00:00Z
date_updated: 2023-05-08T11:03:23Z
department:
- _id: XiFe
doi: 10.1093/pcp/pcv087
extern: '1'
external_id:
  pmid:
  - '26063389'
intvolume: '        56'
issue: '8'
keyword:
- Cell Biology
- Plant Science
- Physiology
- General Medicine
language:
- iso: eng
month: '08'
oa_version: None
page: 1616-1623
pmid: 1
publication: Plant and Cell Physiology
publication_identifier:
  issn:
  - 0032-0781
  - 1471-9053
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: The chromatin remodeler SPLAYED negatively regulates SNC1-mediated immunity
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 56
year: '2015'
...
