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dc.contributor.authorMedeiros, Lea Ann
dc.contributor.authorDennis, Lucas M.
dc.contributor.authorGill, Mark E.
dc.contributor.authorHoubaviy, Hristo
dc.contributor.authorMarkoulaki, Styliani
dc.contributor.authorFu, Dongdong
dc.contributor.authorWhite, Amy C.
dc.contributor.authorKirak, Oktay
dc.contributor.authorSharp, Phillip A.
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorPage, David C
dc.date.accessioned2012-05-02T19:57:58Z
dc.date.available2012-05-02T19:57:58Z
dc.date.issued2011-08
dc.date.submitted2011-01
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/70485
dc.description.abstractMir-290 through mir-295 (mir-290–295) is a mammalian-specific microRNA (miRNA) cluster that, in mice, is expressed specifically in early embryos and embryonic germ cells. Here, we show that mir-290–295 plays important roles in embryonic development as indicated by the partially penetrant lethality of mutant embryos. In addition, we show that in surviving mir-290–295-deficient embryos, female but not male fertility is compromised. This impairment in fertility arises from a defect in migrating primordial germ cells and occurs equally in male and female mutant animals. Male mir-290–295−/− mice, due to the extended proliferative lifespan of their germ cells, are able to recover from this initial germ cell loss and are fertile. Female mir-290–295−/− mice are unable to recover and are sterile, due to premature ovarian failure.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5-F32-HD051190)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant RO1-GM34277)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5R37CA084198)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5R01-HD045022)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant PO1-CA42063)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Core Grant P30-CA14051)en_US
dc.description.sponsorshipHoward Hughes Medical Instituteen_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1111241108en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePNASen_US
dc.titleMir-290–295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defectsen_US
dc.typeArticleen_US
dc.identifier.citationMedeiros, L. A. et al. “Mir-290-295 Deficiency in Mice Results in Partially Penetrant Embryonic Lethality and Germ Cell Defects.” Proceedings of the National Academy of Sciences 108.34 (2011): 14163–14168. Web. ©2011 by the National Academy of Sciences.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverJaenisch, Rudolf
dc.contributor.mitauthorMedeiros, Lea Ann
dc.contributor.mitauthorDennis, Lucas M.
dc.contributor.mitauthorGill, Mark E.
dc.contributor.mitauthorMarkoulaki, Styliani
dc.contributor.mitauthorFu, Dongdong
dc.contributor.mitauthorWhite, Amy C.
dc.contributor.mitauthorKirak, Oktay
dc.contributor.mitauthorSharp, Phillip A.
dc.contributor.mitauthorPage, David C.
dc.contributor.mitauthorJaenisch, Rudolf
dc.relation.journalProceedings of the National Academy of Sciences of the United States of Americaen_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.orderedauthorsMedeiros, L. A.; Dennis, L. M.; Gill, M. E.; Houbaviy, H.; Markoulaki, S.; Fu, D.; White, A. C.; Kirak, O.; Sharp, P. A.; Page, D. C.; Jaenisch, R.en
dc.identifier.orcidhttps://orcid.org/0000-0001-9920-3411
dc.identifier.orcidhttps://orcid.org/0000-0003-1465-1691
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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