Making RISC

被引:403
作者
Kawamata, Tomoko [1 ,2 ]
Tomari, Yukihide [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Univ Tokyo, Dept Med Genome Sci, Bunkyo Ku, Tokyo 1130032, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
关键词
GUIDE-STRAND; RNA CLEAVAGE; MICRORNA MATURATION; ARGONAUTE COMPLEXES; SILENCING COMPLEX; PASSENGER-STRAND; DISTINCT ROLES; SIRNA; SPECIFICITY; RECOGNITION;
D O I
10.1016/j.tibs.2010.03.009
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
It is well established that 20- to 30-nt small RNAs, including small interfering RNAs, microRNAs and Piwi-interacting RNAs, play crucial roles in regulating gene expression and control a surprisingly diverse array of biological processes. These small RNAs cannot work alone: they must form effector ribonucleoprotein complexes RNA-induced silencing complexes (RISCs) - to exert their function. Thus, RISC assembly is a key process in small RNA-mediated silencing. Recent biochemical analyses of RISC assembly, together with new structural studies of Argonaute, the core protein component of RISC, suggest a revised view of how mature RISC, which contains single-stranded guide RNA, is built from small RNAs that are born double-stranded.
引用
收藏
页码:368 / 376
页数:9
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