Regulation of mRNA Translation and Stability by microRNAs

被引:2529
作者
Fabian, Marc Robert [1 ,2 ]
Sonenberg, Nahum [1 ,2 ]
Filipowicz, Witold [3 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ H3G 1Y6, Canada
[3] Friedrich Miescher Inst Biomed Res, CH-4002 Basel, Switzerland
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 79 | 2010年 / 79卷
基金
加拿大健康研究院;
关键词
Argonaute; deadenylation; GW182; microRNA; repression; MIRNA-MEDIATED REPRESSION; RIBOSOME ENTRY SITE; ENCEPHALOMYOCARDITIS VIRUS-RNA; POLY(A) BINDING-PROTEIN; INITIATION-FACTOR; POLY(A)-BINDING PROTEIN; LET-7; MICRORNA; IN-VITRO; P-BODIES; CAENORHABDITIS-ELEGANS;
D O I
10.1146/annurev-biochem-060308-103103
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) are small noncoding RNAs that extensively regulate gene expression in animals, plants, and protozoa. miRNAs function posttranscriptionally by usually base-pairing to the mRNA 3'-untranslated regions to repress protein synthesis by mechanisms that are not fully understood. In this review, we describe principles of miRNA-mRNA interactions and proteins that interact with miRNAs and function in miRNA-mediated repression. We discuss the multiple, often contradictory, mechanisms that miRNAs have been reported to use, which cause translational repression and mRNA decay. We also address the issue of cellular localization of miRNA-mediated events and a role for RNA-binding proteins in activation or relief of miRNA repression.
引用
收藏
页码:351 / 379
页数:29
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