Conversion of pre-RISC to holo-RISC by Ago2 during assembly of RNAi complexes

被引:69
作者
Kim, Kevin
Lee, Young Sik
Carthew, Richard W.
机构
[1] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[2] Korea Univ, Coll Life Sci & Biotechnol, Div Biotechnol, Seoul 136713, South Korea
关键词
RNAi; RISC assembly; Ago2; siRNA; Drosophila; DOUBLE-STRANDED-RNA; CRYSTAL-STRUCTURE; PASSENGER-STRAND; SLICER ACTIVITY; DISTINCT ROLES; DROSOPHILA; SIRNA; INTERFERENCE; ARGONAUTE2; CLEAVAGE;
D O I
10.1261/rna.283207
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
In the Drosophila RNA interference (RNAi) pathway, small interfering RNAs (siRNAs) direct Argonaute2 (Ago2), an endonuclease, within the RNA-induced silencing complex ( RISC) to cleave complementary mRNA targets. In vitro studies have shown that, for each siRNA duplex, RISC retains only one strand, the guide, and releases the other, the passenger, to form a holo-RISC complex. Here, we have isolated a new Ago2 mutant allele and provide, for the first time, in vivo evidence that endogenous Ago2 slicer activity is important to mount an RNAi response in Drosophila. We demonstrate in vivo that efficient removal of the passenger strand from RISC requires the cleavage activity of Ago2. We have also identified a new intermediate complex in the RISC assembly pathway, pre-RISC, in which Ago2 is stably bound to double-stranded siRNA.
引用
收藏
页码:22 / 29
页数:8
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