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Cited 52 time in webofscience Cited 55 time in scopus
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Conserved microRNA miR-8 controls body size in response to steroid signaling in Drosophila

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dc.contributor.authorJin, Hua-
dc.contributor.authorKim, V. Narry-
dc.contributor.authorHyun, Seogang-
dc.date.available2019-05-29T05:40:29Z-
dc.date.issued2012-07-
dc.identifier.issn0890-9369-
dc.identifier.issn1549-5477-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20195-
dc.description.abstractBody size determination is a process that is tightly linked with developmental maturation. Ecdysone, an insect maturation hormone, contributes to this process by antagonizing insulin signaling and thereby suppressing juvenile growth. Here, we report that the microRNA miR-8 and its target, u-shaped (USH), a conserved microRNA/target axis that regulates insulin signaling, are critical for ecdysone-induced body size determination in Drosophila. We found that the miR-8 level is reduced in response to ecdysone, while the USH level is up-regulated reciprocally, and that miR-8 is transcriptionally repressed by ecdysone's early response genes. Furthermore, modulating the miR-8 level correlatively changes the fly body size; either overexpression or deletion of miR-8 abrogates ecdysone-induced growth control. Consistently, perturbation of USH impedes ecdysone's effect on body growth. Thus, miR-8 acts as a molecular rheostat that tunes organismal growth in response to a developmental maturation signal.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherCOLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT-
dc.titleConserved microRNA miR-8 controls body size in response to steroid signaling in Drosophila-
dc.typeArticle-
dc.identifier.doi10.1101/gad.192872.112-
dc.identifier.bibliographicCitationGENES & DEVELOPMENT, v.26, no.13, pp 1427 - 1432-
dc.description.isOpenAccessY-
dc.identifier.wosid000306175400004-
dc.identifier.scopusid2-s2.0-84863685771-
dc.citation.endPage1432-
dc.citation.number13-
dc.citation.startPage1427-
dc.citation.titleGENES & DEVELOPMENT-
dc.citation.volume26-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorbody size-
dc.subject.keywordAuthorecdysone-
dc.subject.keywordAuthorinsulin signaling-
dc.subject.keywordAuthormaturation-
dc.subject.keywordAuthormir-8-
dc.subject.keywordAuthorush-
dc.subject.keywordPlusINSULIN-LIKE PEPTIDES-
dc.subject.keywordPlusPROTHORACIC GLAND-
dc.subject.keywordPlusGROWTH-CONTROL-
dc.subject.keywordPlusECDYSONE-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusMETAMORPHOSIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusWEIGHT-
dc.subject.keywordPlusFLIES-
dc.subject.keywordPlusMELANOGASTER-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaDevelopmental Biology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryDevelopmental Biology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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