Mammalian miRNA RISC Recruits CAF1 and PABP to Affect PABP-Dependent Deadenylation

被引:297
作者
Fabian, Marc R. [1 ,2 ]
Mathonnet, Geraldine [1 ,2 ]
Sundermeier, Thomas [1 ,2 ]
Mathys, Hansruedi [3 ]
Zipprich, Jakob T. [3 ]
Svitkin, Yuri V. [1 ,2 ]
Rivas, Fabiola [4 ,5 ]
Jinek, Martin [6 ]
Wohischlegel, James [7 ]
Doudna, Jennifer A. [6 ]
Chen, Chyi-Ying A. [8 ]
Shyu, Ann-Bin [8 ]
Yates, John R., III [7 ]
Hannon, Gregory J. [4 ,5 ]
Filipowicz, Witold [3 ]
Duchaine, Thomas F. [1 ,2 ]
Sonenberg, Nahum [1 ,2 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Goodman Canc Ctr, Montreal, PQ H3G 1Y6, Canada
[3] Friedrich Miescher Inst Biomed Res, CH-4002 Basel, Switzerland
[4] Cold Spring Harbor Lab, Howard Hughes Med Inst, Cold Spring Harbor, NY 11724 USA
[5] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[6] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[7] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[8] Univ Texas Med Sch, Dept Biochem & Mol Biol, Houston, TX 77030 USA
关键词
MESSENGER-RNA DEADENYLATION; PROTEIN IDENTIFICATION TECHNOLOGY; TRANSLATION INITIATION-FACTOR; POLY(A) BINDING-PROTEIN; 3' UNTRANSLATED REGION; POLY(A)-BINDING PROTEIN; HUMAN-CELLS; GW182; PROTEINS; IN-VITRO; SACCHAROMYCES-CEREVISIAE;
D O I
10.1016/j.molcel.2009.08.004
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) inhibit mRNA expression in general by base pairing to the 3'UTR of target mRNAs and consequently inhibiting translation and/or initiating poly(A) tail deadenylation and mRNA destabilization. Here we examine the mechanism and kinetics of miRNA-mediated deadenylation in mouse Krebs-2 ascites extract. We demonstrate that miRNA-mediated mRNA deadenylation occurs subsequent to initial translational inhibition, indicating a two-step mechanism of miRNA action, which serves to consolidate repression. We show that a let-7 miRNA-loaded RNA-induced silencing complex (miRISC) interacts with the poly(A)-binding protein (PABP) and the CAF1 and CCR4 deadenylases. In addition, we demonstrate that miRNA-mediated deadenylation is dependent upon CAF1 activity and PABP, which serves as a bona fide miRNA coactivator. Importantly, we present evidence that GW182, a core component of the miRISC, directly interacts with PABP via its C-terminal region and that this interaction is required for miRNA-mediated deadenylation.
引用
收藏
页码:868 / 880
页数:13
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