1. Academic Validation
  2. The RNA helicase RIG-I has an essential function in double-stranded RNA-induced innate antiviral responses

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

  • Nat Immunol. 2004 Jul;5(7):730-7. doi: 10.1038/ni1087.
Mitsutoshi Yoneyama 1 Mika Kikuchi Takashi Natsukawa Noriaki Shinobu Tadaatsu Imaizumi Makoto Miyagishi Kazunari Taira Shizuo Akira Takashi Fujita
Affiliations

Affiliation

  • 1 Department of Tumor Cell Biology, Tokyo Metropolitan Institute of Medical Science, Tokyo Metropolitan Organization for Medical Research, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo 113-8613, Japan.
Abstract

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.

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