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dc.contributor.authorUlitsky, Igor
dc.contributor.authorShkumatava, Alena
dc.contributor.authorJan, Calvin H.
dc.contributor.authorSive, Hazel L.
dc.contributor.authorBartel, David
dc.contributor.authorJan, Calvin H.
dc.date.accessioned2014-02-07T17:54:02Z
dc.date.available2014-02-07T17:54:02Z
dc.date.issued2011-12
dc.identifier.issn00928674
dc.identifier.urihttp://hdl.handle.net/1721.1/84684
dc.description.abstractThousands of long intervening noncoding RNAs (lincRNAs) have been identified in mammals. To better understand the evolution and functions of these enigmatic RNAs, we used chromatin marks, poly(A)-site mapping and RNA-Seq data to identify more than 550 distinct lincRNAs in zebrafish. Although these shared many characteristics with mammalian lincRNAs, only 29 had detectable sequence similarity with putative mammalian orthologs, typically restricted to a single short region of high conservation. Other lincRNAs had conserved genomic locations without detectable sequence conservation. Antisense reagents targeting conserved regions of two zebrafish lincRNAs caused developmental defects. Reagents targeting splice sites caused the same defects and were rescued by adding either the mature lincRNA or its human or mouse ortholog. Our study provides a roadmap for identification and analysis of lincRNAs in model organisms and shows that lincRNAs play crucial biological roles during embryonic development with functionality conserved despite limited sequence conservation.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant GM067031)en_US
dc.description.sponsorshipEuropean Molecular Biology Organization (long-term fellowship)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Predoctoral fellowship)en_US
dc.description.sponsorshipHuman Frontier Science Program (Strasbourg, France) (Long-term Fellowship)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2011.11.055en_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.titleConserved Function of lincRNAs in Vertebrate Embryonic Development despite Rapid Sequence Evolutionen_US
dc.typeArticleen_US
dc.identifier.citationUlitsky, Igor, Alena Shkumatava, Calvin H. Jan, Hazel Sive, and David P. Bartel. “Conserved Function of lincRNAs in Vertebrate Embryonic Development despite Rapid Sequence Evolution.” Cell 147, no. 7 (December 2011): 1537-1550. © 2011 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorUlitsky, Igoren_US
dc.contributor.mitauthorShkumatava, Alenaen_US
dc.contributor.mitauthorJan, Calvin H.en_US
dc.contributor.mitauthorSive, Hazel L.en_US
dc.contributor.mitauthorBartel, Daviden_US
dc.relation.journalCellen_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.orderedauthorsUlitsky, Igor; Shkumatava, Alena; Jan, Calvin H.; Sive, Hazel; Bartel, David P.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3872-2856
dc.identifier.orcidhttps://orcid.org/0000-0002-4890-424X
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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