Desperately seeking microRNA targets

被引:404
作者
Thomas, Marshall [1 ,2 ]
Lieberman, Judy [1 ,2 ]
Lal, Ashish [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Childrens Hosp Boston, Immune Dis Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp Boston, Program Cellular & Mol Med, Boston, MA USA
关键词
MAMMALIAN MESSENGER-RNAS; 3' UNTRANSLATED REGIONS; POSTTRANSCRIPTIONAL REGULATION; SYSTEMATIC IDENTIFICATION; CELL-PROLIFERATION; BINDING-SITES; C-ELEGANS; PROTEIN; RECOGNITION; EXPRESSION;
D O I
10.1038/nsmb.1921
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) suppress gene expression by inhibiting translation, promoting mRNA decay or both. Each miRNA may regulate hundreds of genes to control the cell's response to developmental and other environmental cues. The best way to understand the function of a miRNA is to identify the genes that it regulates. Target gene identification is challenging because miRNAs bind to their target mRNAs by partial complementarity over a short sequence, suppression of an individual target gene is often small, and the rules of targeting are not completely understood. Here we review computational and experimental approaches to the identification of miRNA-regulated genes. The examination of changes in gene expression that occur when miRNA expression is altered and biochemical isolation of miRNA-associated transcripts complement target prediction algorithms. Bioinformatic analysis of over-represented pathways and nodes in protein-DNA interactomes formed from experimental candidate miRNA gene target lists can focus attention on biologically significant target genes.
引用
收藏
页码:1169 / 1174
页数:6
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