The Menu of Features that Define Primary MicroRNAs and Enable De Novo Design of MicroRNA Genes

被引:155
作者
Fang, Wenwen [1 ,2 ,3 ]
Bartel, David P. [1 ,2 ,3 ]
机构
[1] MIT, Howard Hughes Med Inst, Cambridge, MA 02142 USA
[2] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
RNAI ENZYME COMPLEX; MICROPROCESSOR COMPLEX; DROSHA-DGCR8; COMPLEX; HUMAN-CELLS; IN-VIVO; DICER; RECOGNITION; DETERMINANTS; MECHANISMS; EXPRESSION;
D O I
10.1016/j.molcel.2015.08.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:131 / 145
页数:15
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