Regulation of interferon-gamma-activated STAT1 by the ubiquitin-proteasome pathway

Science. 1996 Sep 20;273(5282):1717-9. doi: 10.1126/science.273.5282.1717.

Abstract

STAT proteins (signal transducers and activators of transcription) are latent cytoplasmic transcription factors that are phosphorylated by Janus kinases in response to cytokines. Phosphorylated STAT proteins translocate to the nucleus, where they transiently turn on specific sets of cytokine-inducible genes. The mechanism that controls the amounts of activated STAT proteins is not understood. STAT1 proteins activated by interferon-gamma treatment in HeLa cells were shown to be stabilized by a proteasome inhibitor and ubiquitinated in vivo. Thus, the amount of activated STAT1 may be negatively regulated by the ubiquitin-proteasome pathway.

Publication types

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

MeSH terms

  • Cell Nucleus / metabolism
  • Cysteine Endopeptidases / metabolism*
  • Cysteine Proteinase Inhibitors / pharmacology
  • DNA / metabolism
  • DNA-Binding Proteins / metabolism*
  • HeLa Cells
  • Humans
  • Immunoblotting
  • Interferon-gamma / pharmacology*
  • Leupeptins / pharmacology
  • Multienzyme Complexes / metabolism*
  • Mutation
  • Phosphorylation
  • Proteasome Endopeptidase Complex
  • STAT1 Transcription Factor
  • Signal Transduction
  • Trans-Activators / metabolism*
  • Tumor Cells, Cultured
  • Ubiquitins / metabolism*

Substances

  • Cysteine Proteinase Inhibitors
  • DNA-Binding Proteins
  • Leupeptins
  • Multienzyme Complexes
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Trans-Activators
  • Ubiquitins
  • Interferon-gamma
  • DNA
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde