Nallagatla Subba Rao, Hwang Jungwook, Toroney Rebecca, Zheng Xiaofeng, Cameron Craig E, Bevilacqua Philip C
Department of Chemistry, Pennsylvania State University, University Park, PA 16802, USA.
Science. 2007 Nov 30;318(5855):1455-8. doi: 10.1126/science.1147347.
Molecular patterns in pathogenic RNAs can be recognized by the innate immune system, and a component of this response is the interferon-induced enzyme RNA-activated protein kinase (PKR). The major activators of PKR have been proposed to be long double-stranded RNAs. We report that RNAs with very limited secondary structures activate PKR in a 5'-triphosphate-dependent fashion in vitro and in vivo. Activation of PKR by 5'-triphosphate RNA is independent of RIG-I and is enhanced by treatment with type 1 interferon (IFN-alpha). Surveillance of molecular features at the 5' end of transcripts by PKR presents a means of allowing pathogenic RNA to be distinguished from self-RNA. The evidence presented here suggests that this form of RNA-based discrimination may be a critical step in mounting an early immune response.
致病RNA中的分子模式可被先天免疫系统识别,这种反应的一个组成部分是干扰素诱导酶RNA激活蛋白激酶(PKR)。PKR的主要激活剂被认为是长双链RNA。我们报告称,二级结构非常有限的RNA在体外和体内以5'-三磷酸依赖的方式激活PKR。5'-三磷酸RNA对PKR的激活不依赖于RIG-I,并且通过1型干扰素(IFN-α)处理而增强。PKR对转录本5'端分子特征的监测提供了一种区分致病RNA和自身RNA的方法。此处提供的证据表明,这种基于RNA的识别形式可能是启动早期免疫反应的关键步骤。