Redox regulation of fos and jun DNA-binding activity in vitro

Science. 1990 Sep 7;249(4973):1157-61. doi: 10.1126/science.2118682.

Abstract

The proto-oncogenes c-fos and c-jun function cooperatively as inducible transcription factors in signal transduction processes. Their protein products, Fos and Jun, form a heterodimeric complex that interacts with the DNA regulatory element known as the activator protein-1 (AP-1) binding site. Dimerization occurs via interaction between leucine zipper domains and serves to bring into proper juxtaposition a region in each protein that is rich in basic amino acids and that forms a DNA-binding domain. DNA binding of the Fos-Jun heterodimer was modulated by reduction-oxidation (redox) of a single conserved cysteine residue in the DNA-binding domains of the two proteins. Furthermore, a nuclear protein was identified that reduced Fos and Jun and stimulated DNA-binding activity in vitro. These results suggest that transcriptional activity mediated by AP-1 binding factors may be regulated by a redox mechanism.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell-Free System
  • Cysteine / physiology
  • DNA Mutational Analysis
  • DNA-Binding Proteins / drug effects
  • DNA-Binding Proteins / physiology*
  • Diamide / pharmacology
  • Humans
  • In Vitro Techniques
  • Molecular Sequence Data
  • Oxidation-Reduction
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Rats
  • Recombinant Proteins
  • Signal Transduction
  • Structure-Activity Relationship
  • Sulfhydryl Reagents / pharmacology
  • Transcription Factors / physiology*

Substances

  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Recombinant Proteins
  • Sulfhydryl Reagents
  • Transcription Factors
  • Diamide
  • Cysteine