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miR-29 miRNAs activate p53 by targeting p85α and CDC42

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dc.contributor.authorPark, Seong-Yeon-
dc.contributor.authorLee, Jung Hyun-
dc.contributor.authorHa, Minju-
dc.contributor.authorNam, Jin-Wu-
dc.contributor.authorKim, V. Narry-
dc.date.accessioned2021-01-31T08:15:14Z-
dc.date.available2021-01-31T08:15:14Z-
dc.date.created2020-07-16-
dc.date.issued2009-01-
dc.identifier.citationNature Structural and Molecular Biology, Vol.16 No.1, pp.23-29-
dc.identifier.issn1545-9993-
dc.identifier.other107010-
dc.identifier.urihttps://hdl.handle.net/10371/171947-
dc.description.abstractThe tumor suppressor p53 is central to many cellular stress responses. Although numerous protein factors that control p53 have been identified, the role of microRNAs (miRNAs) in regulating p53 remains unexplored. In a screen for miRNAs that modulate p53 activity, we find that miR-29 family members (miR-29a, miR-29b and miR-29c) upregulate p53 levels and induce apoptosis in a p53-dependent manner. We further find that miR-29 family members directly suppress p85a (the regulatory subunit of PI3 kinase) and CDC42 (a Rho family GTPase), both of which negatively regulate p53. Our findings provide new insights into the role of miRNAs in the p53 pathway.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titlemiR-29 miRNAs activate p53 by targeting p85α and CDC42-
dc.typeArticle-
dc.contributor.AlternativeAuthor김빛내리-
dc.identifier.doi10.1038/nsmb.1533-
dc.citation.journaltitleNature Structural and Molecular Biology-
dc.identifier.wosid000262267600008-
dc.identifier.scopusid2-s2.0-58149215802-
dc.citation.endpage29-
dc.citation.number1-
dc.citation.startpage23-
dc.citation.volume16-
dc.identifier.sci000262267600008-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, V. Narry-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusWILD-TYPE P53-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusHUMAN CANCER-
dc.subject.keywordPlusLUNG-CANCER-
dc.subject.keywordPlusMICRORNAS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusRESTORATION-
dc.subject.keywordPlusMIR-34A-
dc.subject.keywordPlusTUMORS-
dc.subject.keywordPlusTRANSACTIVATION-
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

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