Distinct Phases of siRNA Synthesis in an Endogenous RNAi Pathway in C. elegans Soma

被引:150
作者
Gent, Jonathan I. [1 ]
Lamm, Aylet T. [2 ]
Pavelec, Derek M. [4 ,5 ,6 ]
Maniar, Jay M. [1 ]
Parameswaran, Poornima [3 ]
Tao, Li [2 ]
Kennedy, Scott [4 ,5 ]
Fire, Andrew Z. [1 ,2 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
[4] Univ Wisconsin, Dept Med Genet, Madison, WI 53706 USA
[5] Univ Wisconsin, Dept Pharmacol, Madison, WI 53706 USA
[6] Univ Wisconsin, Program Mol & Cellular Pharmacol, Madison, WI 53706 USA
关键词
SMALL INTERFERING RNAS; GERM-LINE DEVELOPMENT; SECONDARY SIRNAS; GENE; POLYMERASE; RDE-1; REVEALS; DCR-1; DNA; TRANSCRIPTS;
D O I
10.1016/j.molcel.2010.01.012
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
Endogenous RNA-directed RNA polymerases (RdRPs) are cellular components capable of synthesizing new complementary RNAs from existing RNA templates. We present evidence for successive engagement of two different RdRPs in an endogenous siRNA-based mechanism targeting specific mRNAs in C. elegans soma. In the initiation stage of this process, a group of mRNA species are chosen as targets for downregulation, leading to accumulation of rare 26 nt 5'-phosphorylated antisense RNAs that depend on the RdRP homolog RRF-3, the Argonaute ERGO-1, DICER, and a series of associated ("ERI") factors. This primary process leads to production of a much more abundant class of 22 nt antisense RNAs, dependent on a secondary RdRP (RRF-1) and associating with at least one distinct Argonaute (NRDE-3). The requirement for two RdRP/Argonaute combinations and initiation by a rare class of uniquely structured siRNAs in this pathway illustrate the caution and flexibility used as biological systems exploit the physiological copying of RNA.
引用
收藏
页码:679 / 689
页数:11
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