Yang Baojun, Li Hongwei
Department of Microbiology, University of Hawaii at Manoa, Honolulu, HI, USA.
Methods Mol Biol. 2011;721:215-29. doi: 10.1007/978-1-61779-037-9_13.
Double-stranded RNA (dsRNA) is the trigger of RNA interference (RNAi)-mediated gene regulation. Dicer processes dsRNAs into short interfering RNAs (siRNAs), which are incorporated into the effector RNA-induced silencing complex (RISC) and direct degradation of homologous target mRNAs. In plants and invertebrates, the RNAi machinery also acts as an antiviral mechanism through production of viral siRNAs by Dicer and silencing of replicating viruses. Viral suppressors of RNAi (VSRs) are encoded by some viruses and serve as a strategy to counteract the RNAi-based antiviral immunity. In this chapter, we describe a Dicer activity assay in extracts prepared from Drosophila melanogaster S2 cells. We also introduce a simple procedure to study VSR activity in the in vitro Dicer assay.
双链RNA(dsRNA)是RNA干扰(RNAi)介导的基因调控的触发因素。Dicer将dsRNA加工成小干扰RNA(siRNA),这些siRNA被整合到效应RNA诱导沉默复合体(RISC)中,并直接降解同源靶标mRNA。在植物和无脊椎动物中,RNAi机制还通过Dicer产生病毒siRNA以及沉默复制中的病毒来发挥抗病毒作用。RNAi病毒抑制因子(VSR)由一些病毒编码,是对抗基于RNAi的抗病毒免疫的一种策略。在本章中,我们描述了一种在从黑腹果蝇S2细胞制备的提取物中进行Dicer活性测定的方法。我们还介绍了一种在体外Dicer测定中研究VSR活性的简单程序。