RAVER1 is a coactivator of MDA5-mediated cellular antiviral response

J Mol Cell Biol. 2013 Apr;5(2):111-9. doi: 10.1093/jmcb/mjt006. Epub 2013 Feb 5.

Abstract

Detection of viral nucleic acids by pattern recognition receptors initiates type I interferon (IFN) induction and innate antiviral response. The RIG-I-like receptors (RLRs), including RIG-I and MDA5, recognize cytoplasmic viral RNA in most cell types and are critically involved in innate antiviral response. RIG-I and MDA5 are structurally related and mediate similar signaling pathways. While the regulation of RIG-I activity has been extensively investigated, little is known about the regulatory mechanisms of MDA5 activity. Here we identified ribonucleoprotein PTB-binding 1 (RAVER1) as a specific MDA5-interacting protein. RAVER1 was associated with MDA5 upon viral infection. Overexpression of RAVER1 at low dosages enhanced MDA5- but not RIG-I-mediated activation of the IFN-β promoter, whereas knockdown of RAVER1 inhibited MDA5- but not RIG-I-mediated induction of downstream antiviral genes. Mechanistically, overexpression of RAVER1 enhanced the binding of MDA5 to its ligand poly(I:C), whereas knockdown of RAVER1 had opposite effect. Our findings suggest that RAVER1 specifically regulates MDA5 activity, revealing a mechanism of differential regulation of MDA5- and RIG-I-mediated innate antiviral response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics
  • Carrier Proteins / immunology*
  • Carrier Proteins / metabolism
  • Cell Line
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / immunology*
  • DEAD-box RNA Helicases / metabolism
  • Herpes Simplex / genetics
  • Herpes Simplex / immunology*
  • Herpes Simplex / metabolism
  • Herpesvirus 1, Human / genetics
  • Herpesvirus 1, Human / immunology*
  • Herpesvirus 1, Human / metabolism
  • Humans
  • Immunity, Innate*
  • Interferon Inducers / pharmacology
  • Interferon-Induced Helicase, IFIH1
  • Nuclear Proteins / genetics
  • Nuclear Proteins / immunology*
  • Nuclear Proteins / metabolism
  • Poly I-C / pharmacology
  • Protein Binding / drug effects
  • Protein Binding / genetics
  • Protein Binding / immunology
  • RNA, Viral / genetics
  • RNA, Viral / immunology*
  • RNA, Viral / metabolism
  • Receptors, Immunologic
  • Ribonucleoproteins

Substances

  • Carrier Proteins
  • Interferon Inducers
  • Nuclear Proteins
  • RAVER1 protein, human
  • RNA, Viral
  • Receptors, Immunologic
  • Ribonucleoproteins
  • RIGI protein, human
  • IFIH1 protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases
  • Interferon-Induced Helicase, IFIH1
  • Poly I-C