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In-depth study of lin-28 suggests selectively conserved let-7 independent mechanism in Drosophila

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dc.contributor.authorLee, Mihye-
dc.contributor.authorThanh My Thi Nguyen-
dc.contributor.authorKim, Kiyoung-
dc.date.accessioned2021-08-11T10:23:29Z-
dc.date.available2021-08-11T10:23:29Z-
dc.date.issued2019-03-01-
dc.identifier.issn0378-1119-
dc.identifier.issn1879-0038-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/4664-
dc.description.abstractLin-28 is a conserved RNA-binding protein that is involved in a wide range of developmental processes and pathogenesis. At the molecular level, Lin-28 blocks the maturation of let-7 and regulates translation of certain mRNA targets. In Drosophila, Lin-28 is reported to play a role in oogenesis, muscle formation, and the symmetric division of adult intestinal stem cells. In this study, we characterized Drosophila Lin-28 through a detailed examination of its temporal and spatial expression. Lin-28 is specifically expressed in embryonic nervous and cardiac systems. However, loss or gain of lin-28 function does not cause any abnormality during embryonic development. Instead, the ubiquitous overexpression of Lin-28 leads to lethality from late larval stage to pupal stage, and eye-specific overexpression causes severe cell loss. The ectopic expression of human Lin28A has the same effect as Drosophila Lin-28, indicating functional conservation in Lin-28 orthologs. We also examined the effect of Lin-28 on let-7 biogenesis through the mutant and overexpression analysis. Lin-28 does not block the production of let-7 in Drosophila, which suggests the let-7 independent pathway as a molecular mechanism of Lin-28.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleIn-depth study of lin-28 suggests selectively conserved let-7 independent mechanism in Drosophila-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.gene.2018.11.017-
dc.identifier.scopusid2-s2.0-85056641862-
dc.identifier.wosid000456753500010-
dc.identifier.bibliographicCitationGene, v.687, pp 64 - 72-
dc.citation.titleGene-
dc.citation.volume687-
dc.citation.startPage64-
dc.citation.endPage72-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusRNA-BINDING PROTEINS-
dc.subject.keywordPlusLIN28 PROTEINS-
dc.subject.keywordPlusMESSENGER-RNAS-
dc.subject.keywordPlusMICRORNA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordPlusTRANSLATION-
dc.subject.keywordPlusREGULATOR-
dc.subject.keywordPlusPANNIER-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorLin-28-
dc.subject.keywordAuthorlet-7-
dc.subject.keywordAuthorRNA binding protein-
dc.subject.keywordAuthorEmbryonic development-
dc.subject.keywordAuthorDrosophila-
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College of Medical Sciences > Department of Medical Biotechnology > 1. Journal Articles
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