Interaction of AP-1 with a cluster of NF-kappa B binding elements in the human TNF promoter region

Biochem Biophys Res Commun. 2001 Nov 23;289(1):25-33. doi: 10.1006/bbrc.2001.5929.

Abstract

Transcriptional activation of the human TNF gene involves multiple regulatory elements whose functional properties vary between stimuli and cell types. Here we have used a COS-7 expression system to dissect the transactivating potential of NF-kappa B binding sites in the human TNF promoter region from other regulatory influences. In this model, NF-kappa B acts largely through a dense cluster of three binding sites located 600 nt upstream of the transcription start site. We show that the transcriptional activity of this complex is highly sensitive to the p65:p50 ratio that is expressed. We demonstrate that the AP-1 complex c-Jun/Fra2 is capable of binding to this region and that this inhibits the transactivating effects of NF-kappa B. These results are suggestive of a complex regulatory element that mediates fine control rather than acting as a simple on-off switch for TNF gene expression.

MeSH terms

  • Animals
  • Binding Sites / genetics
  • COS Cells
  • DNA-Binding Proteins / metabolism
  • Fos-Related Antigen-2
  • Humans
  • NF-kappa B / chemistry
  • NF-kappa B / metabolism*
  • NF-kappa B p50 Subunit
  • Promoter Regions, Genetic*
  • Protein Subunits
  • Proto-Oncogene Proteins c-fos / metabolism
  • Proto-Oncogene Proteins c-jun / metabolism
  • Sequence Deletion
  • Transcription Factor AP-1 / metabolism*
  • Transcription Factor RelA
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Tumor Necrosis Factor-alpha / genetics*

Substances

  • DNA-Binding Proteins
  • FOSL2 protein, human
  • Fos-Related Antigen-2
  • NF-kappa B
  • NF-kappa B p50 Subunit
  • Protein Subunits
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Transcription Factor AP-1
  • Transcription Factor RelA
  • Transcription Factors
  • Tumor Necrosis Factor-alpha