Publication:
Essential role of p18Hamlet/SRCAP-mediated histone H2A.Z chromatin incorporation in muscle differentiation.

dc.contributor.authorCuadrado Garcia, Ana
dc.contributor.authorCorrado, Nadia
dc.contributor.authorPerdiguero, Eusebio
dc.contributor.authorLafarga, Vanesa
dc.contributor.authorMuñoz-Canoves, Pura
dc.contributor.authorNebreda, Angel R
dc.contributor.funderMINISTERIO DE CIENCIA E INNOVACION (ESPAÑA)
dc.contributor.funderFundacion Cientifica de la AECC
dc.contributor.funderEuropean Union (EU)
dc.contributor.funderFUNDACION LA CAIXA
dc.contributor.funderICREA
dc.date.accessioned2025-01-21T12:22:05Z
dc.date.available2025-01-21T12:22:05Z
dc.date.issued2010-06-16
dc.description.abstractThe chromatin-remodelling complex SNF2-related CBP activator protein (SRCAP) regulates chromatin structure in yeast by modulating the exchange of histone H2A for the H2A.Z variant. Here, we have investigated the contribution of H2A.Z-mediated chromatin remodelling to mammalian cell differentiation reprogramming. We show that the SRCAP subunit named ZNHIT1 or p18(Hamlet), which is a substrate of p38 MAPK, is recruited to the myogenin promoter at the onset of muscle differentiation, in a p38 MAPK-dependent manner. We also show that p18(Hamlet) is required for H2A.Z accumulation into this genomic region and for subsequent muscle gene transcriptional activation. Accordingly, downregulation of several subunits or the SRCAP complex impairs muscle gene expression. These results identify SRCAP/H2A.Z-mediated chromatin remodelling as a key early event in muscle differentiation-specific gene expression. We also propose a mechanism by which p38 MAPK-mediated signals are converted into chromatin structural changes, thereby facilitating transcriptional activation during mammalian cell differentiation.
dc.description.peerreviewed
dc.description.tableofcontentsWe are grateful to AL Serrano (UPF) for advice on in vivo analysis of de novo myogenesis and to M Berciano (Universidad de Cantabria) for help with immunofluorescence studies. NC was supported by the Marie Curie-FP6 training project Onco-Train. This work was funded by CNIO and by grants from the Spanish Ministerio de Ciencia e Innovacion (MICINN) (BFU2007-60575, RD06/0020/0083 and SAF2009-09782), the European Commission FP7 program grant 'INFLA-CARE' (EC contract number 223151), Fundacion Cientifica de la AECC and Fundacion La Caixa
dc.format.number12
dc.format.page2014-2025
dc.format.volume29
dc.identifier.citationEMBO J . 2010 Jun 16;29(12):2014-25
dc.identifier.journalEMBO Journal
dc.identifier.pubmedID20473270
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26087
dc.language.isoeng
dc.publisherWiley
dc.relation.projectIDinfo:eu-repo/grantAgreement/MEC//BFU2007-60575/ES/INTEGRACION DE SEÑALES POR P38 MAPK: FUNCIONES FISIOLOGICAS IN VIVO Y MECANISMOS DE REGULACION TUMORAL/
dc.relation.projectIDinfo:eu-repo/grantAgreement/MSC//RD06%2F0020%2F0083/ES/RED TEMÁTICA DE INVESTIGACIÓN COOPERATIVA DEL CANCER/
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//SAF2009-09782/ES/Mecanismos Reguladores De La Regeneracion Y El Crecimiento Del Musculo Esqueletico: Distrofia Muscular/
dc.relation.projectID223151
dc.relation.publisherversionhttp://doi: 10.1038/emboj.2010.85.
dc.repisalud.institucionCNIO
dc.repisalud.orgCNIOCNIO::Grupos de investigación::Grupo de Inestabilidad Genómica
dc.rights.accessRightsopen access
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjecthistone H2A.Z
dc.subjectmyogenesis
dc.subjectp38MAPK
dc.subjectSCRAP
dc.titleEssential role of p18Hamlet/SRCAP-mediated histone H2A.Z chromatin incorporation in muscle differentiation.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublicatione5f71313-2258-41e7-9712-d23295ef6e60
relation.isAuthorOfPublication259ea37c-41fc-4f09-b2f0-a909a24d048b
relation.isAuthorOfPublication.latestForDiscoverye5f71313-2258-41e7-9712-d23295ef6e60

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