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G3BP1 inhibits RNA virus replication by positively regulating RIG-I-mediated cellular antiviral response.

Wenping YangYi RuJingjing RenJuncui BaiJunshu WeiShaozu FuXiangtao LiuHaixue ZhengHaixue Zheng
Published in: Cell death & disease (2019)
Retinoic acid-inducible gene I (RIG-I) is a pattern recognition receptor and is involved in the innate immune response against RNA viruses infection. Here, we demonstrate that the Ras-GTPase-activating protein SH3-domain-binding protein 1 (G3BP1) serves as a positive regulator of the RIG-I-mediated signaling pathway. G3BP1-deficient cells inhibited RNA virus-triggered induction of downstream antiviral genes. Furthermore, we found that G3BP1 inhibited the replication of Sendai virus and vesicular stomatitis virus, indicating a positive regulation of G3BP1 to cellular antiviral responses. Mechanistically, G3BP1 formed a complex with RNF125 and RIG-I, leading to decreased RNF125 via its auto-ubiquitination; thus, promoting expression of RIG-I. Overall, the results suggest a novel mechanism for G3BP1 in the positive regulation of antiviral signaling mediated by RIG-I.
Keyphrases
  • immune response
  • binding protein
  • signaling pathway
  • induced apoptosis
  • poor prognosis
  • oxidative stress
  • dna damage
  • disease virus
  • toll like receptor
  • nucleic acid
  • protein protein