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dc.contributor.authorFang, Wenwen
dc.contributor.authorBartel, David
dc.date.accessioned2018-06-15T13:25:26Z
dc.date.available2018-06-15T13:25:26Z
dc.date.issued2015-09
dc.date.submitted2015-07
dc.identifier.issn1097-2765
dc.identifier.issn1097-4164
dc.identifier.urihttp://hdl.handle.net/1721.1/116324
dc.description.abstractMicroRNAs (miRNAs) are small regulatory RNAs processed from stem-loop regions of primary transcripts (pri-miRNAs), with the choice of stem loops for initial processing largely determining what becomes a miRNA. To identify sequence and structural features influencing this choice, we determined cleavage efficiencies of > 50,000 variants of three human pri-miRNAs, focusing on the regions intractable to previous high-throughput analyses. Our analyses revealed a mismatched motif in the basal stem region, a preference for maintaining or improving base pairing throughout the remainder of the stem, and a narrow stem-length preference of 35 ± 1 base pairs. Incorporating these features with previously identified features, including three primary-sequence motifs, yielded a unifying model defining mammalian pri-miRNAs in which motifs help orient processing and increase efficiency, with the presence of more motifs compensating for structural defects. This model enables generation of artificial pri-miRNAs, designed de novo, without reference to any natural sequence yet processed more efficiently than natural pri-miRNAs.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant NIH GM067031)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.MOLCEL.2015.08.015en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleThe Menu of Features that Define Primary MicroRNAs and Enable De Novo Design of MicroRNA Genesen_US
dc.typeArticleen_US
dc.identifier.citationFang, Wenwen and David P. Bartel. “The Menu of Features That Define Primary MicroRNAs and Enable De Novo Design of MicroRNA Genes.” Molecular Cell 60, 1 (October 2015): 131–145 © 2015 Elsevier Incen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorFang, Wenwen
dc.contributor.mitauthorBartel, David
dc.relation.journalMolecular Cellen_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
dc.date.updated2018-06-12T18:44:47Z
dspace.orderedauthorsFang, Wenwen; Bartel, David P.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3872-2856
mit.licensePUBLISHER_CCen_US


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