Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Mol Cell. 2010 Mar 12;37(5):679-89. doi: 10.1016/j.molcel.2010.01.012. Epub 2010 Jan 28.
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.
内源性 RNA 指导的 RNA 聚合酶(RdRPs)是能够从现有 RNA 模板合成新互补 RNA 的细胞成分。我们提供了证据表明,在靶向秀丽隐杆线虫体特定 mRNA 的内源性 siRNA 机制中,两种不同的 RdRPs 相继参与。在这个过程的起始阶段,一组 mRNA 被选择作为下调的靶标,导致罕见的 26 个核苷酸 5'-磷酸化反义 RNA 的积累,这依赖于 RdRP 同源物 RRF-3、Argonaute ERGO-1、DICER 和一系列相关的("ERI")因子。这个初始过程导致大量 22 个核苷酸的反义 RNA 的产生,这依赖于第二种 RdRP(RRF-1)和至少一个独特的 Argonaute(NRDE-3)的参与。在这条途径中,两种 RdRP/Argonaute 组合的需求以及由独特结构的稀有类 siRNA 引发的需求,说明了生物系统在利用 RNA 的生理复制时所使用的谨慎性和灵活性。