Combinatorial microRNA target predictions

被引:3744
作者
Krek, A
Grun, D
Poy, MN
Wolf, R
Rosenberg, L
Epstein, EJ
MacMenamin, P
da Piedade, I
Gunsalus, KC
Stoffel, M
Rajewsky, N
机构
[1] NYU, Dept Biol, Ctr Comparat Funct Genom, New York, NY 10003 USA
[2] NYU, Dept Phys, New York, NY 10003 USA
[3] Rockefeller Univ, Lab Metab Dis, New York, NY 10021 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1038/ng1536
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs are small noncoding RNAs that recognize and bind to partially complementary sites in the 3' untranslated regions of target genes in animals and, by unknown mechanisms, regulate protein production of the target transcript(1-3). Different combinations of microRNAs are expressed in different cell types and may coordinately regulate cell-specific target genes. Here, we present PicTar, a computational method for identifying common targets of microRNAs. Statistical tests using genome-wide alignments of eight vertebrate genomes, PicTar's ability to specifically recover published microRNA targets, and experimental validation of seven predicted targets suggest that PicTar has an excellent success rate in predicting targets for single microRNAs and for combinations of microRNAs. We find that vertebrate microRNAs target, on average, roughly 200 transcripts each. Furthermore, our results suggest widespread coordinate control executed by microRNAs. In particular, we experimentally validate common regulation of Mtpn by miR-375, miR-124 and let-7b and thus provide evidence for coordinate microRNA control in mammals.
引用
收藏
页码:495 / 500
页数:6
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