C3PO, an Endoribonuclease That Promotes RNAi by Facilitating RISC Activation

被引:194
作者
Liu, Ying [1 ]
Ye, Xuecheng [1 ]
Jiang, Feng [1 ]
Liang, Chunyang [1 ]
Chen, Dongmei [2 ]
Peng, Junmin [2 ]
Kinch, Lisa N. [1 ,3 ]
Grishin, Nick V. [1 ,3 ]
Liu, Qinghua [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
[2] Emory Univ, Dept Human Genet, Ctr Neurodegenerat Dis, Atlanta, GA 30322 USA
[3] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
DROSOPHILA TRANSLIN; SIRNA; MECHANISMS; ARGONAUTE2; COMPLEXES; PROTEIN; CLEAVES; MUTANT; STRAND; R2D2;
D O I
10.1126/science.1176325
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The catalytic engine of RNA interference (RNAi) is the RNA-induced silencing complex (RISC), wherein the endoribonuclease Argonaute and single-stranded small interfering RNA (siRNA) direct target mRNA cleavage. We reconstituted long double-stranded RNA-and duplex siRNA-initiated RISC activities with the use of recombinant Drosophila Dicer-2, R2D2, and Ago2 proteins. We used this core reconstitution system to purify an RNAi regulator that we term C3PO (component 3 promoter of RISC), a complex of Translin and Trax. C3PO is a Mg2+-dependent endoribonuclease that promotes RISC activation by removing siRNA passenger strand cleavage products. These studies establish an in vitro RNAi reconstitution system and identify C3PO as a key activator of the core RNAi machinery.
引用
收藏
页码:750 / 753
页数:4
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