Gregory Richard I, Chendrimada Thimmaiah P, Cooch Neil, Shiekhattar Ramin
The Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
Cell. 2005 Nov 18;123(4):631-40. doi: 10.1016/j.cell.2005.10.022. Epub 2005 Nov 3.
RNA interference is implemented through the action of the RNA-induced silencing complex (RISC). Although Argonaute2 has been identified as the catalytic center of RISC, the RISC polypeptide composition and assembly using short interfering RNA (siRNA) duplexes has remained elusive. Here we show that RISC is composed of Dicer, the double-stranded RNA binding protein TRBP, and Argonaute2. We demonstrate that this complex can cleave target RNA using precursor microRNA (pre-miRNA) hairpin as the source of siRNA. Although RISC can also utilize duplex siRNA, it displays a nearly 10-fold greater activity using the pre-miRNA Dicer substrate. RISC distinguishes the guide strand of the siRNA from the passenger strand and specifically incorporates the guide strand. Importantly, ATP is not required for miRNA processing, RISC assembly, or multiple rounds of target-RNA cleavage. These results define the composition of RISC and demonstrate that miRNA processing and target-RNA cleavage are coupled.
RNA干扰是通过RNA诱导沉默复合体(RISC)的作用来实现的。尽管已经确定Argonaute2是RISC的催化中心,但RISC的多肽组成以及使用小干扰RNA(siRNA)双链体的组装过程仍不清楚。在这里,我们表明RISC由Dicer、双链RNA结合蛋白TRBP和Argonaute2组成。我们证明,该复合体可以使用前体微小RNA(pre-miRNA)发夹作为siRNA来源来切割靶RNA。尽管RISC也可以利用双链siRNA,但使用pre-miRNA Dicer底物时其活性几乎高近10倍。RISC将siRNA的引导链与过客链区分开来,并特异性地纳入引导链。重要的是,miRNA加工、RISC组装或多轮靶RNA切割都不需要ATP。这些结果确定了RISC的组成,并证明miRNA加工和靶RNA切割是偶联的。