Department of Medical Microbiology & Immunology, University of Alberta, 632 Heritage Medical Research Center, Edmonton, AB, T6G 2S2, Canada.
Viruses. 2009 Dec;1(3):523-44. doi: 10.3390/v1030523. Epub 2009 Oct 27.
The interferon-induced double-stranded (ds)RNA-dependent protein kinase (PKR) limits viral replication by an eIF2α-mediated block of translation. Although many negative-strand RNA viruses activate PKR, the responsible RNAs have long remained elusive, as dsRNA, the canonical activator of PKR, has not been detected in cells infected with such viruses. In this review we focus on the activating RNA molecules of different virus families, in particular the negative-strand RNA viruses. We discuss the recently identified non-canonical activators 5'-triphosphate RNA and the vRNP of influenza virus and give an update on strategies of selected RNA and DNA viruses to prevent activation of PKR.
干扰素诱导的双链 (ds)RNA 依赖性蛋白激酶 (PKR) 通过 eIF2α 介导的翻译阻断来限制病毒复制。尽管许多负链 RNA 病毒会激活 PKR,但负责的 RNA 一直难以捉摸,因为 dsRNA 是 PKR 的经典激活剂,在感染此类病毒的细胞中并未检测到。在这篇综述中,我们重点关注不同病毒家族的激活 RNA 分子,特别是负链 RNA 病毒。我们讨论了最近发现的非典型激活剂 5'-三磷酸 RNA 和流感病毒的 vRNP,并更新了选定的 RNA 和 DNA 病毒防止 PKR 激活的策略。