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dc.contributor.authorNam, Jin-Wu
dc.contributor.authorRissland, Olivia S.
dc.contributor.authorAbreu-Goodger, Cei
dc.contributor.authorJan, Calvin H.
dc.contributor.authorAgarwal, Vikram
dc.contributor.authorYildirim, Muhammed A.
dc.contributor.authorRodriguez, Antony
dc.contributor.authorKoppstein, David Neal Pira
dc.contributor.authorBartel, David
dc.contributor.authorRissland, Olivia S.
dc.contributor.authorJan, Calvin H.
dc.contributor.authorYildirim, Muhammed A.
dc.date.accessioned2015-04-02T16:13:11Z
dc.date.available2015-04-02T16:13:11Z
dc.date.issued2014-03
dc.date.submitted2014-01
dc.identifier.issn10972765
dc.identifier.issn1097-4164
dc.identifier.urihttp://hdl.handle.net/1721.1/96328
dc.description.abstractMicroRNA (miRNA) regulation clearly impacts animal development, but the extent to which development—with its resulting diversity of cellular contexts—impacts miRNA regulation is unclear. Here, we compared cohorts of genes repressed by the same miRNAs in different cell lines and tissues and found that target repertoires were largely unaffected, with secondary effects explaining most of the differential responses detected. Outliers resulting from differential direct targeting were often attributable to alternative 3′ UTR isoform usage that modulated the presence of miRNA sites. More inclusive examination of alternative 3′ UTR isoforms revealed that they influence ~10% of predicted targets when comparing any two cell types. Indeed, considering alternative 3′ UTR isoform usage improved prediction of targeting efficacy significantly beyond the improvements observed when considering constitutive isoform usage. Thus, although miRNA targeting is remarkably consistent in different cell types, considering the 3′ UTR landscape helps predict targeting efficacy and explain differential regulation that is observed.en_US
dc.description.sponsorshipKorea (South). Ministry of Education, Science and Technology (MEST) (National Research Foundation of Korea. NRF-2013R1A1A1010185)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant RO1 GM067031)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant K99 GM102319)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.molcel.2014.02.013en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevier Open Archiveen_US
dc.titleGlobal Analyses of the Effect of Different Cellular Contexts on MicroRNA Targetingen_US
dc.typeArticleen_US
dc.identifier.citationNam, Jin-Wu, Olivia S. Rissland, David Koppstein, Cei Abreu-Goodger, Calvin H. Jan, Vikram Agarwal, Muhammed A. Yildirim, Antony Rodriguez, and David P. Bartel. “Global Analyses of the Effect of Different Cellular Contexts on MicroRNA Targeting.” Molecular Cell 53, no. 6 (March 2014): 1031–1043. © 2014 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Programen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorNam, Jin-Wuen_US
dc.contributor.mitauthorRissland, Olivia S.en_US
dc.contributor.mitauthorKoppstein, David Neal Piraen_US
dc.contributor.mitauthorJan, Calvin H.en_US
dc.contributor.mitauthorYildirim, Muhammed A.en_US
dc.contributor.mitauthorBartel, Daviden_US
dc.relation.journalMolecular Cellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsNam, Jin-Wu; Rissland, Olivia S.; Koppstein, David; Abreu-Goodger, Cei; Jan, Calvin H.; Agarwal, Vikram; Yildirim, Muhammed A.; Rodriguez, Antony; Bartel, David P.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3872-2856
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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