Functional relevance of the conserved DNA-binding domain of STAT2

J Biol Chem. 2005 Apr 1;280(13):13029-36. doi: 10.1074/jbc.M500426200. Epub 2005 Jan 24.

Abstract

Several distinct type I interferon (IFN)-inducible STAT2-containing complexes have been identified. For the IFN-stimulated gene factor 3 (ISGF3), STAT1 and IRF-9 mediate IFN-stimulated response element (ISRE) binding, whereas STAT2 provides a potent transactivational domain. ISGF3-independent STAT2-containing complexes, specifically STAT2:1 and STAT2:3, bind a gamma-activated sequence (GAS)-like element, yet the contribution of each STAT to DNA binding is unknown. Moreover, the contribution of these ISGF3-independent STAT2-containing complexes to IFN-inducible responses is not defined. Accordingly, we generated mutant cDNAs, targeting the DNA-binding domain in STAT2. These cDNAs were introduced by transfection into U6A cells lacking STAT2, resulting in a panel of cell lines expressing mutant STAT2 proteins. Studies assessed the sensitivity of U6A cells reconstituted with intact STAT2 (U6A-2) and cells expressing mutant STAT2s (U6A-2E426A,E427A (EE-AA), U6A-2V453I, U6A-2V454I, U6A-2V454A, U6A-2V453I,V454I(VV-II), U6A-2N458A) to IFN-inducible responses. Our data reveal that none of the mutations in the STAT2 DNA-binding domain affected IFN-inducible ISGF3 activation, and only the VV-II mutation restricted antiviral and growth inhibitory responses to IFN. Indeed, U6A-2VV-II cells are refractory to these IFN-inducible biological activities and also exhibit impaired IFN-inducible GAS-driven transcriptional activation and subsequent gene expression. Chromatin immunoprecipitation assays revealed that the VV-II mutation in STAT2 does not abrogate, but reduces the DNA binding activity of STAT2:1 heterodimers. Taken together, these data suggest a role for the conserved DNA-binding domain of STAT2 specific to the activity of ISGF3-independent STAT2-containing complexes.

MeSH terms

  • Cell Nucleus / metabolism
  • Cell Proliferation
  • Chromatin / metabolism
  • Chromatin Immunoprecipitation
  • Conserved Sequence
  • DNA / chemistry
  • DNA / metabolism
  • DNA, Complementary / chemistry
  • DNA, Complementary / metabolism
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / physiology
  • Dimerization
  • Fibroblasts / metabolism
  • Gene Expression Regulation
  • Humans
  • Immunoblotting
  • Interferons / metabolism
  • Luciferases / metabolism
  • Models, Molecular
  • Mutagenesis
  • Mutation
  • Oligonucleotides / chemistry
  • Protein Binding
  • Protein Structure, Tertiary
  • RNA / metabolism
  • STAT2 Transcription Factor
  • Time Factors
  • Trans-Activators / chemistry*
  • Trans-Activators / physiology
  • Transcriptional Activation
  • Transfection
  • Tyrosine / chemistry

Substances

  • Chromatin
  • DNA, Complementary
  • DNA-Binding Proteins
  • Oligonucleotides
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • Trans-Activators
  • Tyrosine
  • RNA
  • DNA
  • Interferons
  • Luciferases