Andersson M Gunnar, Haasnoot P C Joost, Xu Ning, Berenjian Saideh, Berkhout Ben, Akusjärvi Göran
Department of Medical Biochemistry and Microbiology, Uppsala Biomedical Center, Sweden.
J Virol. 2005 Aug;79(15):9556-65. doi: 10.1128/JVI.79.15.9556-9565.2005.
We show that human adenovirus inhibits RNA interference (RNAi) at late times of infection by suppressing the activity of two key enzyme systems involved, Dicer and RNA-induced silencing complex (RISC). To define the mechanisms by which adenovirus blocks RNAi, we used a panel of mutant adenoviruses defective in virus-associated (VA) RNA expression. The results show that the virus-associated RNAs, VA RNAI and VA RNAII, function as suppressors of RNAi by interfering with the activity of Dicer. The VA RNAs bind Dicer and function as competitive substrates squelching Dicer. Further, we show that VA RNAI and VA RNAII are processed by Dicer, both in vitro and during a lytic infection, and that the resulting short interfering RNAs (siRNAs) are incorporated into active RISC. Dicer cleaves the terminal stem of both VA RNAI and VA RNAII. However, whereas both strands of the VA RNAI-specific siRNA are incorporated into RISC, the 3' strand of the VA RNAII-specific siRNA is selectively incorporated during a lytic infection. In summary, our work shows that adenovirus suppresses RNAi during a lytic infection and gives insight into the mechanisms of RNAi suppression by VA RNA.
我们发现,人类腺病毒在感染后期通过抑制两个关键酶系统——Dicer和RNA诱导沉默复合体(RISC)的活性来抑制RNA干扰(RNAi)。为了确定腺病毒阻断RNAi的机制,我们使用了一组病毒相关(VA)RNA表达缺陷的突变腺病毒。结果表明,病毒相关RNA,即VA RNAI和VA RNAII,通过干扰Dicer的活性发挥RNAi抑制子的作用。VA RNA与Dicer结合,作为竞争性底物抑制Dicer。此外,我们发现VA RNAI和VA RNAII在体外和裂解感染期间均被Dicer加工,产生的小干扰RNA(siRNA)被整合到活性RISC中。Dicer切割VA RNAI和VA RNAII的末端茎环。然而,虽然VA RNAI特异性siRNA的两条链都被整合到RISC中,但在裂解感染期间,VA RNAII特异性siRNA的3'链被选择性整合。总之,我们的研究表明腺病毒在裂解感染期间抑制RNAi,并深入了解了VA RNA抑制RNAi的机制。