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dc.rights.licenseopenen_US
dc.contributor.authorHU, G.
dc.contributor.authorHUANG, B.
dc.contributor.authorWANG, K.
dc.contributor.authorFRASSE, P.
dc.contributor.authorMAZA, E.
dc.contributor.authorDJARI, A.
dc.contributor.authorBENHAMED, M.
hal.structure.identifierEcophysiologie et Génomique Fonctionnelle de la Vigne [UMR EGFV]
dc.contributor.authorGALLUSCI, Philippe
dc.contributor.authorLI, Z.
dc.contributor.authorZOUINE, M.
dc.contributor.authorBOUZAYEN, M.
dc.date.accessioned2021-11-29T09:12:26Z
dc.date.available2021-11-29T09:12:26Z
dc.date.issued2021
dc.identifier.issn0028-646Xen_US
dc.identifier.otherhttps://www.ebi.ac.uk/ena/dataen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/123938
dc.description.abstractEnFruit formation comprises a series of developmental transitions among which the fruit set process is essential in determining crop yield. Yet, our understanding of the epigenetic landscape remodelling associated with the flower-to-fruit transition remains poor. We investigated the epigenetic and transcriptomic reprogramming underlying pollination-dependent and auxin-induced flower-to-fruit transitions in the tomato (Solanum lycopersicum) using combined genomewide transcriptomic profiling, global ChIP-sequencing and whole genomic DNA bisulfite sequencing (WGBS). Variation in the expression of the overwhelming majority of genes was associated with change in histone mark distribution, whereas changes in DNA methylation concerned a minor fraction of differentially expressed genes. Reprogramming of genes involved in processes instrumental to fruit set correlated with their H3K9ac or H3K4me3 marking status but not with changes in cytosine methylation, indicating that histone posttranslational modifications rather than DNA methylation are associated with the remodelling of the epigenetic landscape underpinning the flower-to-fruit transition. Given the prominent role previously assigned to DNA methylation in reprogramming key genes of the transition to ripening, the outcome of the present study supports the idea that the two main developmental transitions in fleshy fruit and the underlying transcriptomic reprogramming are associated with different modes of epigenetic regulations.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enAuxin
dc.subject.enCas9
dc.subject.enCRISPR
dc.subject.enDNA methylation
dc.subject.enFruit set
dc.subject.enHistone posttranslational modification
dc.subject.enPollination
dc.subject.enSolanum lycopersicum
dc.title.enHistone posttranslational modifications rather than DNA methylation underlie gene reprogramming in pollination-dependent and pollination-independent fruit set in tomato
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/nph.16902en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
bordeaux.journalNew Phytologisten_US
bordeaux.page902-919en_US
bordeaux.volume229en_US
bordeaux.hal.laboratoriesEcophysiologie et Génomique Fonctionnelle de la Vigne (EGFV) - UMR 1287en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux Sciences Agroen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
dc.rights.ccCC BY-NC-NDen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=New%20Phytologist&rft.date=2021&rft.volume=229&rft.issue=2&rft.spage=902-919&rft.epage=902-919&rft.eissn=0028-646X&rft.issn=0028-646X&rft.au=HU,%20G.&HUANG,%20B.&WANG,%20K.&FRASSE,%20P.&MAZA,%20E.&rft.genre=article


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