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dc.contributor.authorKojima, Mina
dc.contributor.authorde Rooij, Dirk G.
dc.contributor.authorPage, David C
dc.date.accessioned2020-06-09T19:58:52Z
dc.date.available2020-06-09T19:58:52Z
dc.date.issued2019-02
dc.date.submitted2018-11
dc.identifier.issn2050-084X
dc.identifier.urihttps://hdl.handle.net/1721.1/125746
dc.description.abstractThe germ line provides the cellular link between generations of multicellular organisms, its cells entering the meiotic cell cycle only once each generation. However, the mechanisms governing this initiation of meiosis remain poorly understood. Here, we examined cells undergoing meiotic initiation in mice, and we found that initiation involves the dramatic upregulation of a transcriptional network of thousands of genes whose expression is not limited to meiosis. This broad gene expression program is directly upregulated by STRA8, encoded by a germ cell-specific gene required for meiotic initiation. STRA8 binds its own promoter and those of thousands of other genes, including meiotic prophase genes, factors mediating DNA replication and the G1-S cell-cycle transition, and genes that promote the lengthy prophase unique to meiosis I. We conclude that, in mice, the robust amplification of this extraordinarily broad transcription program by a common factor triggers initiation of meiosis.en_US
dc.language.isoen
dc.publishereLife Sciences Publications, Ltden_US
dc.relation.isversionof10.7554/ELIFE.43738en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceeLifeen_US
dc.titleAmplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in miceen_US
dc.typeArticleen_US
dc.identifier.citationKojima, Mina, Dirk G. de Rooij, and David C. Page, "Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice." eLife 2019 (Feb. 2019): doi 10.7554/ELIFE.43738 ©2019 Author(s)en_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journaleLifeen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-01-15T15:43:23Z
dspace.date.submission2020-01-15T15:43:25Z
mit.journal.volume2019en_US
mit.metadata.statusComplete


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