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An autoinhibitory mechanism modulates MAVS activity in antiviral innate immune response.

Abstract
In response to virus infection, RIG-I senses viral RNA and activates the adaptor protein MAVS, which then forms prion-like filaments and stimulates a specific signalling pathway leading to type I interferon production to restrict virus proliferation. However, the mechanisms by which MAVS activity is regulated remain elusive. Here we identify distinct regions of MAVS responsible for activation of transcription factors interferon regulatory factor 3 (IRF3) and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB). These IRF3- and NF-κB-stimulating regions recruit preferential TNF receptor-associated factors (TRAFs) for downstream signalling. Strikingly, these regions' activities are inhibited by their respective adjacent regions in quiescent MAVS. Our data thus show that an autoinhibitory mechanism modulates MAVS activity in unstimulated cells and, on viral infection, individual regions of MAVS are released following MAVS filament formation to activate antiviral signalling cascades.
AuthorsYuheng Shi, Bofeng Yuan, Nan Qi, Wenting Zhu, Jingru Su, Xiaoyan Li, Peipei Qi, Dan Zhang, Fajian Hou
JournalNature communications (Nat Commun) Vol. 6 Pg. 7811 (Jul 17 2015) ISSN: 2041-1723 [Electronic] England
PMID26183716 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adaptor Proteins, Signal Transducing
  • IPS-1 protein, mouse
  • Interferon Regulatory Factor-3
  • Interferon Type I
  • MAVS protein, human
  • NF-kappa B
  • RNA, Viral
  • Receptors, Immunologic
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
  • RIGI protein, human
  • Ddx58 protein, mouse
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases
Topics
  • Adaptor Proteins, Signal Transducing (genetics, immunology)
  • Animals
  • Cell Line
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases (immunology)
  • Gene Knockout Techniques
  • HEK293 Cells
  • Humans
  • Immunity, Innate (immunology)
  • Interferon Regulatory Factor-3 (immunology)
  • Interferon Type I (immunology)
  • Mice
  • NF-kappa B (immunology)
  • RNA, Viral (immunology)
  • Receptors, Immunologic
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
  • Vesiculovirus

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