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dc.contributor.authorJunker, Jan Philipp
dc.contributor.authorGill, Mark E.
dc.contributor.authorMueller, Jacob L.
dc.contributor.authorvan Oudenaarden, Alexander
dc.contributor.authorSoh, Ying Qi Shirleen
dc.contributor.authorPage, David C
dc.date.accessioned2015-11-09T16:45:58Z
dc.date.available2015-11-09T16:45:58Z
dc.date.issued2015-09
dc.date.submitted2015-06
dc.identifier.issn1553-7404
dc.identifier.issn1553-7390
dc.identifier.urihttp://hdl.handle.net/1721.1/99763
dc.description.abstractThe chromosomal program of meiotic prophase, comprising events such as laying down of meiotic cohesins, synapsis between homologs, and homologous recombination, must be preceded and enabled by the regulated induction of meiotic prophase genes. This gene regulatory program is poorly understood, particularly in organisms with a segregated germline. We characterized the gene regulatory program of meiotic prophase as it occurs in the mouse fetal ovary. By profiling gene expression in the mouse fetal ovary in mutants with whole tissue and single-cell techniques, we identified 104 genes expressed specifically in pre-meiotic to pachytene germ cells. We characterized the regulation of these genes by 1) retinoic acid (RA), which induces meiosis, 2) Dazl, which is required for germ cell competence to respond to RA, and 3) Stra8, a downstream target of RA required for the chromosomal program of meiotic prophase. Initial induction of practically all identified meiotic prophase genes requires Dazl. In the presence of Dazl, RA induces at least two pathways: one Stra8-independent, and one Stra8-dependent. Genes vary in their induction by Stra8, spanning fully Stra8-independent, partially Stra8-independent, and fully Stra8-dependent. Thus, Stra8 regulates the entirety of the chromosomal program but plays a more nuanced role in governing the gene expression program. We propose that Stra8-independent gene expression enables the stockpiling of selected meiotic structural proteins prior to the commencement of the chromosomal program. Unexpectedly, we discovered that Stra8 is required for prompt down-regulation of itself and Rec8. Germ cells that have expressed and down-regulated Stra8 are refractory to further Stra8 expression. Negative feedback of Stra8, and subsequent resistance to further Stra8 expression, may ensure a single, restricted pulse of Stra8 expression. Collectively, our findings reveal a gene regulatory logic by which germ cells prepare for the chromosomal program of meiotic prophase, and ensure that it is induced only once.en_US
dc.description.sponsorshipHoward Hughes Medical Instituteen_US
dc.description.sponsorshipEuropean Research Council (Grant ERC-AdG 294325-GeneNoiseControl)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-GM068957)en_US
dc.description.sponsorshipHoward Hughes Medical Institute (International Student Research Fellowship)en_US
dc.description.sponsorshipWhitehead Institute for Biomedical Research (Abraham Siegal Fellowship)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pgen.1005531en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePublic Library of Scienceen_US
dc.titleA Gene Regulatory Program for Meiotic Prophase in the Fetal Ovaryen_US
dc.typeArticleen_US
dc.identifier.citationSoh, Y. Q. Shirleen, Jan Philipp Junker, Mark E. Gill, Jacob L. Mueller, Alexander van Oudenaarden, and David C. Page. “A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary.” Edited by R. Scott Hawley. PLOS Genetics 11, no. 9 (September 17, 2015): e1005531.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorSoh, Y. Q. Shirleenen_US
dc.contributor.mitauthorJunker, Jan Philippen_US
dc.contributor.mitauthorGill, Mark E.en_US
dc.contributor.mitauthorvan Oudenaarden, Alexanderen_US
dc.contributor.mitauthorPage, David C.en_US
dc.relation.journalPLOS Geneticsen_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.orderedauthorsSoh, Y. Q. Shirleen; Junker, Jan Philipp; Gill, Mark E.; Mueller, Jacob L.; van Oudenaarden, Alexander; Page, David C.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9920-3411
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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