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dc.contributor.authorWilliams, Eric O
dc.contributor.authorTaylor, Amy K.
dc.contributor.authorLim, Rachelle A.
dc.contributor.authorKim, Daniel M.
dc.contributor.authorGuarente, Leonard Pershing
dc.contributor.authorBell, Eric L.
dc.date.accessioned2017-02-23T20:34:10Z
dc.date.available2017-02-23T20:34:10Z
dc.date.issued2016-10
dc.date.submitted2016-06
dc.identifier.issn2211-1247
dc.identifier.urihttp://hdl.handle.net/1721.1/107140
dc.description.abstractThe enhancer landscape is dramatically restructured as naive preimplantation epiblasts transition to the post-implantation state of primed pluripotency. A key factor in this process is Otx2, which is upregulated during the early stages of this transition and ultimately recruits Oct4 to a different set of enhancers. In this study, we discover that the acetylation status of Oct4 regulates the induction of the primed pluripotency gene network. Maintenance of the naive state requires the NAD-dependent deacetylase, SirT1, which deacetylates Oct4. The activity of SirT1 is reduced during the naive-to-primed transition; Oct4 becomes hyper-acetylated and binds to an Otx2 enhancer to induce Otx2 expression. Induction of Otx2 causes the reorganization of acetylated Oct4 and results in the induction of the primed pluripotency gene network. Regulation of Oct4 by SirT1 may link stem cell development to environmental conditions, and it may provide strategies to manipulate epiblast cell state.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.description.sponsorshipGlenn Foundation for Medical Researchen_US
dc.description.sponsorshipAmerican Cancer Societyen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2016.09.046en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElsevieren_US
dc.titleSirtuin 1 Promotes Deacetylation of Oct4 and Maintenance of Naive Pluripotencyen_US
dc.typeArticleen_US
dc.identifier.citationWilliams, Eric O. et al. “Sirtuin 1 Promotes Deacetylation of Oct4 and Maintenance of Naive Pluripotency.” Cell Reports 17.3 (2016): 809–820.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentPaul F. Glenn Center for Biology of Aging Research (Massachusetts Institute of Technology)en_US
dc.contributor.mitauthorWilliams, Eric O
dc.contributor.mitauthorTaylor, Amy K.
dc.contributor.mitauthorBell, Eric L
dc.contributor.mitauthorLim, Rachelle A.
dc.contributor.mitauthorKim, Daniel M.
dc.contributor.mitauthorGuarente, Leonard Pershing
dc.relation.journalCell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWilliams, Eric O.; Taylor, Amy K.; Bell, Eric L.; Lim, Rachelle; Kim, Daniel M.; Guarente, Leonarden_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4064-2510
mit.licensePUBLISHER_CCen_US


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