The molecular choreography of IRF4 and IRF8 with immune system partners

Cold Spring Harb Symp Quant Biol. 2013:78:101-4. doi: 10.1101/sqb.2013.78.020305. Epub 2014 Apr 21.

Abstract

The transcription factors IRF4 and IRF8 represent immune-specific members of the interferon regulatory family. They play major roles in controlling the development and functioning of innate and adaptive cells. Genes encoding these factors appear to have been coopted by the immune system via gene duplication and divergence of regulatory and protein coding sequences to enable the acquisition of unique molecular properties and functions. Unlike other members of the IRF family, IRF4 and IRF8 do not activate transcription of Type 1 interferon genes or positively regulate interferon-induced gene expression. Instead, they bind to unusual composite Ets-IRF or AP-1-IRF elements with specific Ets or AP-1 family transcription factors, respectively, and regulate the expression of diverse sets of immune response genes in innate as well as adaptive cells.

MeSH terms

  • Adaptive Immunity
  • Animals
  • Cell Differentiation
  • DNA / chemistry
  • Dendritic Cells / cytology
  • Gene Expression
  • Gene Expression Regulation
  • Humans
  • Immunity, Innate
  • Interferon Regulatory Factors / physiology*
  • Interferons / metabolism
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Protein c-ets-1 / metabolism
  • Transcription Factor AP-1 / metabolism
  • Transcription Factors / genetics
  • Transcription, Genetic

Substances

  • Interferon Regulatory Factors
  • Proto-Oncogene Protein c-ets-1
  • Transcription Factor AP-1
  • Transcription Factors
  • interferon regulatory factor-4
  • interferon regulatory factor-8
  • DNA
  • Interferons