RNAi Factors Are Present and Active in Human Cell Nuclei

被引:289
作者
Gagnon, Keith T. [1 ]
Li, Liande [1 ]
Chu, Yongjun [1 ]
Janowski, Bethany A. [1 ]
Corey, David R. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pharmacol & Biochem, Dallas, TX 75390 USA
来源
CELL REPORTS | 2014年 / 6卷 / 01期
基金
美国国家卫生研究院;
关键词
SMALL INTERFERING RNA; MAMMALIAN-CELLS; GENE-EXPRESSION; HUMAN RISC; ARGONAUTE PROTEINS; SILENCING COMPLEX; MESSENGER-RNA; DUPLEX RNAS; TARGET RNAS; ACTIVATION;
D O I
10.1016/j.celrep.2013.12.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNAi is widely appreciated as a powerful regulator of mRNA translation in the cytoplasm of mammalian cells. However, the presence and activity of RNAi factors in the mammalian nucleus has been the subject of considerable debate. Here, we show that Argonaute-2 (Ago2) and RNAi factors Dicer, TRBP, and TRNC6A/GW182 are in the human nucleus and associate together in multiprotein complexes. Small RNAs can silence nuclear RNA and guide site-specific cleavage of the targeted RNA, demonstrating that RNAi can function in the human nucleus. Nuclear Dicer is active and miRNAs are bound to nuclear Ago2, consistent with the existence of nuclear miRNA pathways. Notably, we do not detect loading of duplex small RNAs in nuclear extracts and known loading factors are absent. These results extend RNAi into the mammalian nucleus and suggest that regulation of RNAi via small RNA loading of Ago2 differs between the cytoplasm and the nucleus.
引用
收藏
页码:211 / 221
页数:11
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