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Cited 2 time in webofscience Cited 2 time in scopus
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HuR stabilizes a polyadenylated form of replication-dependent histone mRNAs under stress conditions

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dc.contributor.authorRyu, Incheol-
dc.contributor.authorPark, Yeonkyoung-
dc.contributor.authorSeo, Jwa-Won-
dc.contributor.authorPark, Ok Hyun-
dc.contributor.authorHa, Hongseok-
dc.contributor.authorNam, Jin-Wu-
dc.contributor.authorKim, Yoon Ki-
dc.date.accessioned2021-08-02T12:27:05Z-
dc.date.available2021-08-02T12:27:05Z-
dc.date.created2021-05-12-
dc.date.issued2019-02-
dc.identifier.issn0892-6638-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/15054-
dc.description.abstractAll metazoan mRNAs have a poly(A) tail at the 3′ end with the exception of replication-dependent histone (RDH) mRNAs, which end in a highly conserved stem-loop (SL) structure. However, a subset of RDH mRNAs are reported to be polyadenylated under physiologic conditions. The molecular details of the biogenesis of polyadenylated RDH [poly(A)+ RDH] mRNAs remain unknown. In this study, our genome-wide analyses reveal that puromycin treatment or UVC irradiation stabilizes poly(A)+ RDH mRNAs, relative to canonical RDH mRNAs, which end in an SL structure. We demonstrate that the stabilization of poly(A)+ RDH mRNAs occurs in a translation-independent manner and is regulated via human antigen R (HuR) binding to the extended 3′ UTR under stress conditions. Our data suggest that HuR regulates the expression of poly(A)+ RDH mRNAs.—Ryu, I., Park, Y., Seo, J.-W., Park, O. H., Ha, H., Nam, J.-W., Kim, Y. K. HuR stabilizes a polyadenylated form of replication-dependent histone mRNAs under stress conditions. FASEB J. 33, 2680–2693 (2019). www.fasebj.org-
dc.language영어-
dc.language.isoen-
dc.publisherFEDERATION AMER SOC EXP BIOL-
dc.titleHuR stabilizes a polyadenylated form of replication-dependent histone mRNAs under stress conditions-
dc.typeArticle-
dc.contributor.affiliatedAuthorNam, Jin-Wu-
dc.identifier.doi10.1096/fj.201800431R-
dc.identifier.scopusid2-s2.0-85061059167-
dc.identifier.wosid000457296600092-
dc.identifier.bibliographicCitationFASEB JOURNAL, v.33, no.2, pp.2680 - 2693-
dc.relation.isPartOfFASEB JOURNAL-
dc.citation.titleFASEB JOURNAL-
dc.citation.volume33-
dc.citation.number2-
dc.citation.startPage2680-
dc.citation.endPage2693-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaLife Sciences & Biomedicine - Other Topics-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusLOOP-BINDING-PROTEIN-
dc.subject.keywordPlusALTERNATIVE POLYADENYLATION-
dc.subject.keywordPlusSTEM-LOOP-
dc.subject.keywordPlusRAPID DEGRADATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusCLEAVAGE-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusINTERACTS-
dc.subject.keywordAuthormRNA stability-
dc.subject.keywordAuthor3UTR-
dc.subject.keywordAuthorpolyadenylation signal-
dc.subject.keywordAuthorUVC-
dc.identifier.urlhttps://faseb.onlinelibrary.wiley.com/doi/full/10.1096/fj.201800431R-
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