Genome-wide microRNA screening reveals that the evolutionary conserved miR-9a regulates body growth by targeting sNPFR1/NPYR

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dc.contributor.authorSuh, Yoon Seokko
dc.contributor.authorBhat, Shreelathako
dc.contributor.authorHong, Seung-Hyunko
dc.contributor.authorShin, Minjungko
dc.contributor.authorBahk, Suhyoungko
dc.contributor.authorCho, Kyung Sangko
dc.contributor.authorKim, Seung-Whanko
dc.contributor.authorLee, Kyu-Sunko
dc.contributor.authorKim, Young-Joonko
dc.contributor.authorJones, Walton Dko
dc.contributor.authorYu, Kweonko
dc.date.accessioned2016-04-15T03:09:49Z-
dc.date.available2016-04-15T03:09:49Z-
dc.date.created2015-09-01-
dc.date.created2015-09-01-
dc.date.created2015-09-01-
dc.date.issued2015-07-
dc.identifier.citationNATURE COMMUNICATIONS, v.6-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://hdl.handle.net/10203/204011-
dc.description.abstractMicroRNAs (miRNAs) regulate many physiological processes including body growth. Insulin/ IGF signalling is the primary regulator of animal body growth, but the extent to which miRNAs act in insulin-producing cells (IPCs) is unclear. Here we generate a UAS-miRNA library of Drosophila stocks and perform a genetic screen to identify miRNAs whose overexpression in the IPCs inhibits body growth in Drosophila. Through this screen, we identify miR-9a as an evolutionarily conserved regulator of insulin signalling and body growth. IPC-specific miR-9a overexpression reduces insulin signalling and body size. Of the predicted targets of miR-9a, we find that loss of miR-9a enhances the level of sNPFR1. We show via an in vitro binding assay that miR-9a binds to sNPFR1 mRNA in insect cells and to the mammalian orthologue NPY2R in rat insulinoma cells. These findings indicate that the conserved miR-9a regulates body growth by controlling sNPFR1/NPYR-mediated modulation of insulin signalling.-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleGenome-wide microRNA screening reveals that the evolutionary conserved miR-9a regulates body growth by targeting sNPFR1/NPYR-
dc.typeArticle-
dc.identifier.wosid000358858100037-
dc.identifier.scopusid2-s2.0-84936775014-
dc.type.rimsART-
dc.citation.volume6-
dc.citation.publicationnameNATURE COMMUNICATIONS-
dc.identifier.doi10.1038/ncomms8693-
dc.contributor.localauthorJones, Walton D-
dc.contributor.nonIdAuthorSuh, Yoon Seok-
dc.contributor.nonIdAuthorHong, Seung-Hyun-
dc.contributor.nonIdAuthorShin, Minjung-
dc.contributor.nonIdAuthorCho, Kyung Sang-
dc.contributor.nonIdAuthorKim, Seung-Whan-
dc.contributor.nonIdAuthorLee, Kyu-Sun-
dc.contributor.nonIdAuthorKim, Young-Joon-
dc.contributor.nonIdAuthorYu, Kweon-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusINSULIN-LIKE PEPTIDES-
dc.subject.keywordPlusNEUROPEPTIDE-Y-
dc.subject.keywordPlusDROSOPHILA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusCELLS-
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