MicroRNA targeting specificity in mammals: Determinants beyond seed pairing

被引:2939
作者
Grimson, Andrew
Farh, Kyle Kai-How
Johnston, Wendy K.
Garrett-Engele, Philip
Lim, Lee P.
Bartel, David P.
机构
[1] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[4] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[5] Rosetta Inpharmat, Seattle, WA 98109 USA
关键词
D O I
10.1016/j.molcel.2007.06.017
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
Mammalian microRNAs (miRNAs) pair to 3 ' UTRs of mRNAs to direct their posttranscriptional repression. Important for target recognition are similar to 7 nt sites that match the seed region of the miRNA. However, these seed matches are not always sufficient for repression, indicating that other characteristics help specify targeting. By combining computational and experimental approaches, we uncovered five general features of site context that boost site efficacy: AU-rich nucleotide composition near the site, proximity to sites for coexpressed miRNAs (which leads to cooperative action), proximity to residues pairing to miRNA nucleotides 1316, positioning within the 3 ' UTR at least 15 nt from the stop codon, and positioning away from the center of long UTRs. A model combining these context determinants quantitatively predicts site performance both for exogenously added miRNAs and for endogenous miRNA-message interactions. Because it predicts site efficacy without recourse to evolutionary conservation, the model also identifies effective nonconserved sites and siRNA off-targets.
引用
收藏
页码:91 / 105
页数:15
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