| Literature DB >> 18048689 |
Subba Rao Nallagatla1, Jungwook Hwang, Rebecca Toroney, Xiaofeng Zheng, Craig E Cameron, Philip C Bevilacqua.
Abstract
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.Entities:
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Year: 2007 PMID: 18048689 DOI: 10.1126/science.1147347
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728