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dc.contributor.authorKim, SoonKap
dc.contributor.authorPiquerez, Sophie J M
dc.contributor.authorRamirez-Prado, Juan S
dc.contributor.authorMastorakis, Emmanouil
dc.contributor.authorVeluchamy, Alaguraj
dc.contributor.authorLatrasse, David
dc.contributor.authorManza-Mianza, Deborah
dc.contributor.authorBrik-Chaouche, Rim
dc.contributor.authorHuang, Ying
dc.contributor.authorRodriguez-Granados, Natalia Y
dc.contributor.authorConcia, Lorenzo
dc.contributor.authorBlein, Thomas
dc.contributor.authorCiterne, Sylvie
dc.contributor.authorBendahmane, Abdelhafid
dc.contributor.authorBergounioux, Catherine
dc.contributor.authorCrespi, Martin
dc.contributor.authorMahfouz, Magdy M.
dc.contributor.authorRaynaud, Cécile
dc.contributor.authorHirt, Heribert
dc.contributor.authorNtoukakis, Vardis
dc.contributor.authorBenhamed, Moussa
dc.date.accessioned2020-12-07T07:51:05Z
dc.date.available2020-12-07T07:51:05Z
dc.date.issued2020-05-13
dc.date.submitted2019-10-16
dc.identifier.citationGCN5 modulates salicylic acid homeostasis by regulating H3K14ac levels at the 5' and 3' ends of its target genes. (2020). Nucleic Acids Research. doi:10.1093/nar/gkaa369
dc.identifier.issn0305-1048
dc.identifier.pmid32396165
dc.identifier.doi10.1093/nar/gkaa369
dc.identifier.urihttp://hdl.handle.net/10754/666299
dc.description.abstractThe modification of histones by acetyl groups has a key role in the regulation of chromatin structure and transcription. The Arabidopsis thaliana histone acetyltransferase GCN5 regulates histone modifications as part of the Spt-Ada-Gcn5 Acetyltransferase (SAGA) transcriptional coactivator complex. GCN5 was previously shown to acetylate lysine 14 of histone 3 (H3K14ac) in the promoter regions of its target genes even though GCN5 binding did not systematically correlate with gene activation. Here, we explored the mechanism through which GCN5 controls transcription. First, we fine-mapped its GCN5 binding sites genome-wide and then used several global methodologies (ATAC-seq, ChIP-seq and RNA-seq) to assess the effect of GCN5 loss-of-function on the expression and epigenetic regulation of its target genes. These analyses provided evidence that GCN5 has a dual role in the regulation of H3K14ac levels in their 5' and 3' ends of its target genes. While the gcn5 mutation led to a genome-wide decrease of H3K14ac in the 5' end of the GCN5 down-regulated targets, it also led to an increase of H3K14ac in the 3' ends of GCN5 up-regulated targets. Furthermore, genome-wide changes in H3K14ac levels in the gcn5 mutant correlated with changes in H3K9ac at both 5' and 3' ends, providing evidence for a molecular link between the depositions of these two histone modifications. To understand the biological relevance of these regulations, we showed that GCN5 participates in the responses to biotic stress by repressing salicylic acid (SA) accumulation and SA-mediated immunity, highlighting the role of this protein in the regulation of the crosstalk between diverse developmental and stress-responsive physiological programs. Hence, our results demonstrate that GCN5, through the modulation of H3K14ac levels on its targets, controls the balance between biotic and abiotic stress responses and is a master regulator of plant-environmental interactions.
dc.description.sponsorshipAgence Nationale de la Recherche (ANR) [EPICLISPE ANR-18-CE20-0015]; Institut Universitaire de France (IUF); Biotechnology and Biological Science Research Council [BB/L019345/1, BB/M017982/1 to V.N., in part]; V.N. is also supported by the Royal Society. Funding for open access charge: ANR research grant.
dc.publisherOxford University Press (OUP)
dc.relation.urlhttps://academic.oup.com/nar/article/48/11/5953/5836186
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/)
dc.titleGCN5 modulates salicylic acid homeostasis by regulating H3K14ac levels at the 5' and 3' ends of its target genes.
dc.typeArticle
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentPlant Science
dc.contributor.departmentDesert Agriculture Initiative
dc.identifier.journalNucleic acids research
dc.identifier.pmcidPMC7293002
dc.eprint.versionPublisher's Version/PDF
dc.contributor.institutionInstitute of Plant Sciences Paris-Saclay (IPS2), UMR 9213/UMR1403, CNRS, INRA, Université Paris-Sud, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Bâtiment 630, 91405 Orsay, France.
dc.contributor.institutionSchool of Life Sciences and Warwick Integrative Synthetic Biology Centre, University of Warwick, Coventry CV4 7AL, UK.
dc.contributor.institutionInstitut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, Versailles 78000, France.
dc.identifier.volume48
dc.identifier.issue11
dc.identifier.pages5953-5966
kaust.personVeluchamy, Alaguraj
kaust.personMahfouz, Magdy M.
kaust.personHirt, Heribert
dc.date.accepted2020-05-02
dc.identifier.eid2-s2.0-85086522843
refterms.dateFOA2020-12-07T07:56:36Z


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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.