Iwasaki Shintaro, Tomari Yukihide
Institute of Molecular and Cellular Biosciences, The University of Tokyo, Bunkyo-ku, Tokyo, 113-0032, Japan.
RNA Systems Biochemistry Laboratory, RIKEN, Wako, Saitama, 351-0198, Japan.
Methods Mol Biol. 2018;1680:131-143. doi: 10.1007/978-1-4939-7339-2_9.
Small RNAs, including small interfering RNAs (siRNAs) and microRNAs (miRNAs), silence protein expression from target mRNAs bearing their complementary sequences, via the formation of the effector complex called RNA-induced silencing complex (RISC). Although the mechanism of RISC assembly has been studied for nearly two decades, the detailed mechanism has still remained unclear in part due to the lack of a pure reconstitution system. Recently, we identified all the core proteins necessary for RISC assembly in flies and successfully recapitulated the assembly of catalytically active RISC with eight recombinant proteins. The reconstitution system provides a versatile framework for detailed studies of RISC assembly, including single molecule analysis as described in another chapter in this issue.
小RNA,包括小干扰RNA(siRNA)和微小RNA(miRNA),通过形成称为RNA诱导沉默复合体(RISC)的效应复合体,使携带与其互补序列的靶mRNA的蛋白质表达沉默。尽管RISC组装机制已研究了近二十年,但由于缺乏纯重组系统,详细机制仍部分不明。最近,我们鉴定出果蝇中RISC组装所需的所有核心蛋白,并成功地用八种重组蛋白重现了具有催化活性的RISC的组装。该重组系统为详细研究RISC组装提供了一个通用框架,包括本期另一章中所述的单分子分析。