The RNA helicase RIG-I has an essential function in double-stranded RNA-induced innate antiviral responses

被引:3131
作者
Yoneyama, M
Kikuchi, M
Natsukawa, T
Shinobu, N
Imaizumi, T
Miyagishi, M
Taira, K
Akira, S
Fujita, T
机构
[1] Tokyo Metropolitan Org Med Res, Tokyo Metropolitan Inst Med Sci, Dept Tumor Cell Biol, Bunkyo Ku, Tokyo 1138613, Japan
[2] Hirosaki Univ, Sch Med, Dept Vasc Biol, Hirosaki, Aomori 0368562, Japan
[3] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
[4] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
D O I
10.1038/ni1087
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intracellular double-stranded RNA (dsRNA) is a chief sign of replication for many viruses. Host mechanisms detect the dsRNA and initiate antiviral responses. In this report, we identify retinoic acid inducible gene I (RIG-I), which encodes a DExD/H box RNA helicase that contains a caspase recruitment domain, as an essential regulator for dsRNA-induced signaling, as assessed by functional screening and assays. A helicase domain with intact ATPase activity was responsible for the dsRNA-mediated signaling. The caspase recruitment domain transmitted 'downstream' signals, resulting in the activation of transcription factors NF-kappaB and IRF-3. Subsequent gene activation by these factors induced antiviral functions, including type I interferon production. Thus, RIG-I is key in the detection and subsequent eradication of the replicating viral genomes.
引用
收藏
页码:730 / 737
页数:8
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