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Conserved microRNA miR-8 controls body size in response to steroid signaling in Drosophila

DC Field Value Language
dc.contributor.authorJin, Hua-
dc.contributor.authorKim, V. Narry-
dc.contributor.authorHyun, Seogang-
dc.date.accessioned2021-01-31T08:12:34Z-
dc.date.available2021-01-31T08:12:34Z-
dc.date.created2020-07-16-
dc.date.created2020-07-16-
dc.date.issued2012-07-
dc.identifier.citationGenes and Development, Vol.26 No.13, pp.1427-1432-
dc.identifier.issn0890-9369-
dc.identifier.other107051-
dc.identifier.urihttps://hdl.handle.net/10371/171901-
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.language영어-
dc.publisherCold Spring Harbor Laboratory Press-
dc.titleConserved microRNA miR-8 controls body size in response to steroid signaling in Drosophila-
dc.typeArticle-
dc.contributor.AlternativeAuthor김빛내리-
dc.identifier.doi10.1101/gad.192872.112-
dc.citation.journaltitleGenes and Development-
dc.identifier.wosid000306175400004-
dc.identifier.scopusid2-s2.0-84863685771-
dc.citation.endpage1432-
dc.citation.number13-
dc.citation.startpage1427-
dc.citation.volume26-
dc.identifier.sci000306175400004-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, V. Narry-
dc.type.docTypeArticle-
dc.description.journalClass1-
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.subject.keywordAuthorbody size-
dc.subject.keywordAuthorecdysone-
dc.subject.keywordAuthorinsulin signaling-
dc.subject.keywordAuthormaturation-
dc.subject.keywordAuthormir-8-
dc.subject.keywordAuthorush-
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

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