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dc.contributor.authorGuo, Huili
dc.contributor.authorIngolia, Nicholas T.
dc.contributor.authorWeissman, Jonathan S.
dc.contributor.authorBartel, David
dc.date.accessioned2012-08-29T20:43:55Z
dc.date.available2012-08-29T20:43:55Z
dc.date.issued2010-06
dc.date.submitted2010-02
dc.identifier.issn0028-0836
dc.identifier.issn1476-4687
dc.identifier.urihttp://hdl.handle.net/1721.1/72447
dc.description.abstractMicroRNAs (miRNAs) are endogenous ~22-nucleotide RNAs that mediate important gene-regulatory events by pairing to the mRNAs of protein-coding genes to direct their repression. Repression of these regulatory targets leads to decreased translational efficiency and/or decreased mRNA levels, but the relative contributions of these two outcomes have been largely unknown, particularly for endogenous targets expressed at low-to-moderate levels. Here, we use ribosome profiling to measure the overall effects on protein production and compare these to simultaneously measured effects on mRNA levels. For both ectopic and endogenous miRNA regulatory interactions, lowered mRNA levels account for most (≥84%) of the decreased protein production. These results show that changes in mRNA levels closely reflect the impact of miRNAs on gene expression and indicate that destabilization of target mRNAs is the predominant reason for reduced protein output.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nature09267en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleMammalian microRNAs predominantly act to decrease target mRNA levelsen_US
dc.typeArticleen_US
dc.identifier.citationGuo, Huili et al. “Mammalian microRNAs Predominantly Act to Decrease Target mRNA Levels.” Nature 466.7308 (2010): 835–840.en_US
dc.contributor.departmentmove to dc.description.sponsorshipen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.approverBartel, David
dc.contributor.mitauthorGuo, Huili
dc.contributor.mitauthorBartel, David
dc.relation.journalNatureen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsGuo, Huili; Ingolia, Nicholas T.; Weissman, Jonathan S.; Bartel, David P.en
dc.identifier.orcidhttps://orcid.org/0000-0002-3872-2856
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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