The amino acid residues immediately carboxyl-terminal to the tyrosine phosphorylation site contribute to interleukin 6-specific activation of signal transducer and activator of transcription 3

J Biol Chem. 1997 Apr 4;272(14):9550-5. doi: 10.1074/jbc.272.14.9550.

Abstract

Signal transducers and activators of transcription (Stat) proteins play an important role in signaling through a variety of cytokine and growth factor receptors. Each of the Stat proteins is activated in a ligand-specific manner. Only the Src homology 2 (SH2) domains of Stat1 and Stat2 are critical for the ligand-specific activation of interferon signaling. In this study we determined the domains in Stat3 protein that contribute to interleukin 6 (IL-6)-specific phosphorylation. Based on evidence that Stat3, but not Stat1, is activated in the presence of low levels of IL-6 and soluble IL-6 receptor, we constructed various swap mutants between Stat3 and Stat1 and examined their response to IL-6 after their transient expression into COS7 cells. The region upstream of the SH2 domain was exchangeable between Stat1 and Stat3, whereas the region carboxyl-terminal to the SH2 domain of Stat3 was critical to phosphorylation by IL-6. However, unlike Stat1 and Stat2 in interferon signaling, the swap mutant in which 5 amino acid residues just carboxyl-terminal to the tyrosine phosphorylation site (Tyr705) in Stat3 was replaced by the corresponding region derived from Stat1 was not phosphorylated in response to IL-6. Substituting 1 amino acid (Lys709) at position +4 relative to Tyr705 abolished the tyrosine phosporylation of Stat3 in response to IL-6. Co-immunoprecipitation experiments demonstrated that these mutants were associated with gp130 at an extent similar to wild-type Stat3. Taken together, these results show that the amino acid residues immediately carboxyl-terminal to the tyrosine phosphorylation site are involved in IL-6-specific activation of Stat3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / chemistry*
  • Acute-Phase Proteins / metabolism
  • Amino Acid Sequence
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / metabolism
  • Enzyme Activation
  • Humans
  • Interleukin-6 / chemistry
  • Interleukin-6 / metabolism*
  • Molecular Sequence Data
  • Phosphorylation
  • STAT1 Transcription Factor
  • STAT3 Transcription Factor
  • Signal Transduction*
  • Structure-Activity Relationship
  • Trans-Activators / chemistry*
  • Trans-Activators / metabolism
  • Tyrosine / metabolism*
  • src Homology Domains

Substances

  • Acute-Phase Proteins
  • DNA-Binding Proteins
  • Interleukin-6
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Trans-Activators
  • Tyrosine