A combined computational-experimental approach predicts human microRNA targets

被引:552
作者
Kiriakidou, M
Nelson, PT
Kouranov, A
Fitziev, P
Bouyioukos, C
Mourelatos, Z [1 ]
Hatzigeorgiou, A
机构
[1] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Engn, Ctr Bioinformat, Philadelphia, PA 19104 USA
关键词
microRNA; microRNA targets; microRNP; argonaute; bioinformatics; RNAi;
D O I
10.1101/gad.1184704
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A new paradigm of gene expression regulation has emerged recently with the discovery of microRNAs (miRNAs). Most, if not all, miRNAs are thought to control gene expression, mostly by base pairing with miRNA-recognition elements (MREs) found in their messenger RNA (mRNA) targets. Although a large number of human miRNAs have been reported, many of their mRNA targets remain unknown. Here we used a combined bioinformatics and experimental approach to identify important rules governing miRNA-MRE recognition that allow prediction of human miRNA targets. We describe a computational program, "DIANA-microT", that identifies mRNA targets for animal miRNAs and predicts mRNA targets, bearing single MREs, for human and mouse miRNAs.
引用
收藏
页码:1165 / 1178
页数:14
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