Overlapping and distinct mechanisms regulating IRF-3 and IRF-7 function

J Interferon Cytokine Res. 2002 Jan;22(1):49-58. doi: 10.1089/107999002753452656.

Abstract

Recent molecular, biochemical, and gene disruption studies have demonstrated the essential role of interferon (IFN) regulatory factor-3, (IRF-3) and IRF-7 in the activation of type I IFN gene expression and the induction of the antiviral state. Both transcription factors share structural and functional properties, as well as a common mechanism of activation through C-terminal phosphorylation. The purpose of this review is to summarize recent investigations indicating that similar signalling pathways are likely involved in the activation of IRF-3 and IRF-7. Moreover, unique biochemical events, such as coactivator association and differential recognition of cis-acting elements, also illustrate the capacity of IRF-3 and IRF-7 to selectively regulate type I IFN and IFN-stimulated gene (ISG) expression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Humans
  • Interferon Regulatory Factor-3
  • Interferon Regulatory Factor-7
  • Phosphorylation
  • Protein Structure, Tertiary
  • Response Elements
  • Signal Transduction
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*
  • Transcription Factors / physiology
  • Transcriptional Activation
  • Viruses / pathogenicity

Substances

  • DNA-Binding Proteins
  • IRF3 protein, human
  • IRF7 protein, human
  • Interferon Regulatory Factor-3
  • Interferon Regulatory Factor-7
  • Transcription Factors