A Parsimonious Model for Gene Regulation by miRNAs

被引:399
作者
Djuranovic, Sergej [1 ]
Nahvi, Ali [1 ]
Green, Rachel [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
关键词
MEDIATED TRANSLATIONAL REPRESSION; MESSENGER-RNA DEGRADATION; STRUCTURAL BASIS; PROTEIN-SYNTHESIS; CRYSTAL-STRUCTURE; LET-7; MICRORNA; GW182; PROTEINS; HUMAN-CELLS; PAZ DOMAIN; HUMAN AGO2;
D O I
10.1126/science.1191138
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) and small interfering RNAs (siRNAs) act with the Argonaute family of proteins to regulate target messenger RNAs (mRNAs) posttranscriptionally. SiRNAs typically induce endonucleolytic cleavage of mRNA with near-perfect complementarity. For targets with less complementarity, both translational repression and mRNA destabilization mechanisms have been implicated in miRNA-mediated gene repression, although the timing, coupling, and relative importance of these events have not been determined. Here, we review gene-specific and global approaches that probe miRNA function and mechanism, looking for a unifying model. More systematic analyses of the molecular specificities of the core components coupled with analysis of the relative timing of the different events will ultimately shed light on the mechanism of miRNA-mediated repression.
引用
收藏
页码:550 / 553
页数:4
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