dc.contributor.author | Fang, Wenwen | |
dc.contributor.author | Bartel, David | |
dc.date.accessioned | 2018-06-15T13:25:26Z | |
dc.date.available | 2018-06-15T13:25:26Z | |
dc.date.issued | 2015-09 | |
dc.date.submitted | 2015-07 | |
dc.identifier.issn | 1097-2765 | |
dc.identifier.issn | 1097-4164 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/116324 | |
dc.description.abstract | MicroRNAs (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.sponsorship | National Institutes of Health (U.S.) (Grant NIH GM067031) | en_US |
dc.publisher | Elsevier BV | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1016/J.MOLCEL.2015.08.015 | en_US |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs License | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
dc.source | PMC | en_US |
dc.title | The Menu of Features that Define Primary MicroRNAs and Enable De Novo Design of MicroRNA Genes | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Fang, 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 Inc | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.mitauthor | Fang, Wenwen | |
dc.contributor.mitauthor | Bartel, David | |
dc.relation.journal | Molecular Cell | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2018-06-12T18:44:47Z | |
dspace.orderedauthors | Fang, Wenwen; Bartel, David P. | en_US |
dspace.embargo.terms | N | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-3872-2856 | |
mit.license | PUBLISHER_CC | en_US |