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分子伴侣 HSP90 促进植物 RNA 诱导沉默复合物的体外组装。

In vitro assembly of plant RNA-induced silencing complexes facilitated by molecular chaperone HSP90.

机构信息

Division of Plant Sciences, National Institute of Agrobiological Sciences (NIAS), 2-1-2 Kannondai Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Mol Cell. 2010 Jul 30;39(2):282-91. doi: 10.1016/j.molcel.2010.05.014. Epub 2010 Jun 3.

Abstract

RNA-induced silencing complexes (RISCs) play central roles in posttranscriptional gene silencing. In plants, the mechanism of RISC assembly has remained elusive due to the lack of cell-free systems that recapitulate the process. In this report, we demonstrate that plant AGO1 protein synthesized by in vitro translation using an extract of evacuolated tobacco protoplasts incorporates synthetic small interfering RNA (siRNA) and microRNA (miRNA) duplexes to form RISCs that sequester the single-stranded siRNA guide strand and miRNA strand, respectively. The formed RISCs were able to recognize and cleave the complementary target RNAs. In this system, the siRNA duplex was incorporated into HSP90-bound AGO1, and subsequent removal of the passenger strand was triggered by ATP hydrolysis by HSP90. Removal of the siRNA passenger strand required the ribonuclease activity of AGO1, while that of the miRNA star strand did not. Based on these results, the mechanism of plant RISC formation is discussed.

摘要

RNA 诱导的沉默复合物(RISCs)在后转录基因沉默中发挥核心作用。在植物中,由于缺乏能够重现该过程的无细胞系统,RISC 组装的机制仍然难以捉摸。在本报告中,我们证明了使用抽空烟草原生质体提取物进行体外翻译合成的植物 AGO1 蛋白可以将合成的小干扰 RNA(siRNA)和 microRNA(miRNA)双链体组装成 RISCs,分别将单链 siRNA 引导链和 miRNA 链隔离。形成的 RISCs 能够识别并切割互补的靶 RNA。在这个系统中,siRNA 双链体被并入 HSP90 结合的 AGO1 中,随后通过 HSP90 的 ATP 水解触发过客链的去除。siRNA 过客链的去除需要 AGO1 的核糖核酸酶活性,而 miRNA 星链则不需要。基于这些结果,讨论了植物 RISC 形成的机制。

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