Please use this identifier to cite or link to this item: https://doi.org/10.7554/eLife.38389
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dc.titleImportance of miRNA stability and alternative primary miRNA isoforms in gene regulation during Drosophila development
dc.contributor.authorZhou L.
dc.contributor.authorLim M.Y.T.
dc.contributor.authorKaur P.
dc.contributor.authorSaj A.
dc.contributor.authorBortolamiol-Becet D.
dc.contributor.authorGopal V.
dc.contributor.authorTolwinski N.
dc.contributor.authorTucker-Kellogg G.
dc.contributor.authorOkamura K.
dc.date.accessioned2019-03-12T09:03:35Z
dc.date.available2019-03-12T09:03:35Z
dc.date.issued2018
dc.identifier.citationZhou L., Lim M.Y.T., Kaur P., Saj A., Bortolamiol-Becet D., Gopal V., Tolwinski N., Tucker-Kellogg G., Okamura K. (2018). Importance of miRNA stability and alternative primary miRNA isoforms in gene regulation during Drosophila development. eLife 7 : e38389. ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.38389
dc.identifier.issn2050084X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/152217
dc.description.abstractMature microRNAs (miRNAs) are processed from primary transcripts (pri-miRNAs), and their expression is controlled at transcriptional and post-transcriptional levels. However, how regulation at multiple levels achieves precise control remains elusive. Using published and new datasets, we profile a time course of mature and pri-miRNAs in Drosophila embryos and reveal the dynamics of miRNA production and degradation as well as dynamic changes in pri-miRNA isoform selection. We found that 5? nucleotides influence stability of mature miRNAs. Furthermore, distinct half-lives of miRNAs from the mir-309 cluster shape their temporal expression patterns, and the importance of rapid degradation of the miRNAs in gene regulation is detected as distinct evolutionary signatures at the target sites in the transcriptome. Finally, we show that rapid degradation of miR-3/-309 may be important for regulation of the planar cell polarity pathway component Vang. Altogether, the results suggest that complex mechanisms regulate miRNA expression to support normal development. ? Zhou et al.
dc.publishereLife Sciences Publications Ltd
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentYALE-NUS COLLEGE
dc.contributor.departmentSTATISTICS & APPLIED PROBABILITY
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.7554/eLife.38389
dc.description.sourcetitleeLife
dc.description.volume7
dc.description.pagee38389
dc.published.statepublished
dc.grant.idNRF
dc.grant.id2P40OD010949
dc.grant.idTLL
dc.grant.idMOE2014-T2-2-039
dc.grant.idR01-NS083833
dc.grant.idR01-GM083300
dc.grant.fundingagencyNational Research Foundation
dc.grant.fundingagencyNIH, National Institutes of Health
dc.grant.fundingagencyTemasek Life Sciences Laboratory
dc.grant.fundingagencyACRF, Australian Cancer Research Foundation
dc.grant.fundingagencyFNIH, Foundation for the National Institutes of Health
dc.grant.fundingagencyFNIH, Foundation for the National Institutes of Health
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