Determinants of targeting by endogenous and exogenous microRNAs and siRNAs

被引:290
作者
Nielsen, Cydney B.
Shomron, Noam
Sandberg, Rickard
Hornstein, Eran
Kitzman, Jacob
Burge, Christopher B.
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
关键词
target prediction; Dicer knockout; RNAi; miR; mouse embryonic fibroblast;
D O I
10.1261/rna.768207
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
Vertebrate mRNAs are frequently targeted for post-transcriptional repression by microRNAs ( miRNAs) through mechanisms involving pairing of 39 UTR seed matches to bases at the 59 end of miRNAs. Through analysis of expression array data following miRNA or siRNA overexpression or inhibition, we found that mRNA fold change increases multiplicatively (i.e., log-additively) with seed match count and that a single 8 mer seed match mediates down-regulation comparable to two 7 mer seed matches. We identified several targeting determinants that enhance seed match- associated mRNA repression, including the presence of adenosine opposite miRNA base 1 and of adenosine or uridine opposite miRNA base 9, independent of complementarity to the siRNA/miRNA. Increased sequence conservation in the; 50 bases 59 and 39 of the seed match and increased AU content 39 of the seed match were each independently associated with increased mRNA down-regulation. All of these determinants are enriched in the vicinity of conserved miRNA seed matches, supporting their activity in endogenous miRNA targeting. Together, our results enable improved siRNA off-target prediction, allow integrated ranking of conserved and nonconserved miRNA targets, and show that targeting by endogenous and exogenous miRNAs/siRNAs involves similar or identical determinants.
引用
收藏
页码:1894 / 1910
页数:17
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