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The endogenous siRNA pathway in Drosophila impacts stress resistance and lifespan by regulating metabolic homeostasis

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dc.contributor.authorLim, Do-Hwan-
dc.contributor.authorOh, Chun-Taek-
dc.contributor.authorLee, Langho-
dc.contributor.authorHong, Jae-Sang-
dc.contributor.authorNoh, Su-Hyun-
dc.contributor.authorHwang, Seungwoo-
dc.contributor.authorKim, Sungchan-
dc.contributor.authorHan, Sung-Jun-
dc.contributor.authorLee, Young Sik-
dc.date.accessioned2021-09-07T07:37:03Z-
dc.date.available2021-09-07T07:37:03Z-
dc.date.created2021-06-19-
dc.date.issued2011-10-03-
dc.identifier.issn0014-5793-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/111395-
dc.description.abstractSmall non-coding RNAs regulate gene expression in a sequence-specific manner. In Drosophila, Dicer-2 (Dcr-2) functions in the biogenesis of endogenous small interfering RNAs (endo-siRNAs). We identified 21 distinct proteins that exhibited a >= 1.5-fold change as a consequence of loss of dcr-2 function. Most of these were metabolic genes implicated in stress resistance and aging. dcr-2 Mutants had reduced lifespan and were hypersensitive to oxidative, endoplasmic reticulum, starvation, and cold stresses. Furthermore, loss of dcr-2 function led to abnormal lipid and carbohydrate metabolism. Our results suggest roles for the endo-siRNA pathway in metabolic regulation and defense against stress and aging in Drosophila. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectRNA PATHWAY-
dc.subjectDISTINCT ROLES-
dc.subjectMESSENGER-RNAS-
dc.subjectDICER-2-
dc.subjectGENE-
dc.subjectLONGEVITY-
dc.subjectVIRUSES-
dc.subjectDEFENSE-
dc.subjectINSULIN-
dc.subjectBIND-
dc.titleThe endogenous siRNA pathway in Drosophila impacts stress resistance and lifespan by regulating metabolic homeostasis-
dc.typeArticle-
dc.contributor.affiliatedAuthorHong, Jae-Sang-
dc.contributor.affiliatedAuthorLee, Young Sik-
dc.identifier.doi10.1016/j.febslet.2011.08.034-
dc.identifier.scopusid2-s2.0-80053240762-
dc.identifier.wosid000295473600024-
dc.identifier.bibliographicCitationFEBS LETTERS, v.585, no.19, pp.3079 - 3085-
dc.relation.isPartOfFEBS LETTERS-
dc.citation.titleFEBS LETTERS-
dc.citation.volume585-
dc.citation.number19-
dc.citation.startPage3079-
dc.citation.endPage3085-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusRNA PATHWAY-
dc.subject.keywordPlusDISTINCT ROLES-
dc.subject.keywordPlusMESSENGER-RNAS-
dc.subject.keywordPlusDICER-2-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusLONGEVITY-
dc.subject.keywordPlusVIRUSES-
dc.subject.keywordPlusDEFENSE-
dc.subject.keywordPlusINSULIN-
dc.subject.keywordPlusBIND-
dc.subject.keywordAuthorEndogenous siRNA-
dc.subject.keywordAuthorDicer-2-
dc.subject.keywordAuthorStress response-
dc.subject.keywordAuthorLifespan-
dc.subject.keywordAuthorMetabolic homeostasis-
dc.subject.keywordAuthorDrosophila-
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