p38 MAPK enhances STAT1-dependent transcription independently of Ser-727 phosphorylation

Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):12859-64. doi: 10.1073/pnas.192264999. Epub 2002 Sep 13.

Abstract

The transcription factor signal transducer and activator of transcription 1 (STAT1) requires phosphorylation at both Tyr-701 and Ser-727 for full activation. IFN-gamma induces phosphorylation of both residues, whereas stress signals like UV or lipopolysaccharide stimulate phosphorylation of Ser-727 only. Using p38alpha mitogen-activated protein kinase (MAPK)-deficient cells, we show that the stress-induced phosphorylation of Ser-727 requires p38alpha MAPK activity, whereas IFN-gamma-stimulated Ser-727 phosphorylation occurs independently of the p38alpha pathway. Consistently, IFN-gamma stimulated expression of the STAT1 target gene IRF1 to a similar extent in both wild-type and p38alpha-deficient cells. However, stress-induced activation of the p38 MAPK pathway considerably enhanced the IFN-gamma-induced expression of both the endogenous IRF1 gene and a reporter driven by the IFN-gamma-activated sequence element of the IRF1 promoter. This enhancement occurred independently of increased phosphorylation of Ser-727 by the p38 pathway. Taken together, these results demonstrate an interaction between IFN-gamma signaling and the p38 pathway that leads to increased transcriptional activation by STAT1 independently of phosphorylation at Ser-727.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Blotting, Western
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation
  • Humans
  • Interferon-gamma / metabolism
  • Luciferases / metabolism
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism
  • Mitogen-Activated Protein Kinases / physiology*
  • NF-kappa B / metabolism
  • Phosphorylation
  • Precipitin Tests
  • Promoter Regions, Genetic
  • Protein Binding
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT1 Transcription Factor
  • Serine / metabolism
  • Signal Transduction
  • Trans-Activators / metabolism*
  • Transcription, Genetic*
  • Transfection
  • Tumor Cells, Cultured
  • Ultraviolet Rays
  • p38 Mitogen-Activated Protein Kinases

Substances

  • DNA-Binding Proteins
  • NF-kappa B
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Stat1 protein, mouse
  • Trans-Activators
  • Serine
  • Interferon-gamma
  • Luciferases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases