The cAMP response element binding protein, CREB, is a potent inhibitor of diverse transcriptional activators

Nucleic Acids Res. 1993 Jun 25;21(12):2907-11. doi: 10.1093/nar/21.12.2907.

Abstract

Cyclic AMP response element binding protein (CREB) activates transcription of cAMP response element (CRE)-containing promoters following an elevation of intracellular cAMP. Here we show that CREB and the highly related protein ATF-1 are also potent transcription inhibitors. Strikingly, CREB inhibits transcription of multiple activators, whose DNA-binding domains and activation regions are unrelated to one another. Inhibition requires that the CREB dimerization and DNA-binding domains are intact. However, inhibition is not dependent upon the presence of a CRE in the promoter, and does not involve heterodimer formation between CREB and the activator. The ability of an activator protein to inhibit transcription in such a promiscuous fashion has not been previously reported.

Publication types

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

MeSH terms

  • Activating Transcription Factors
  • Animals
  • Binding Sites
  • Blood Proteins / genetics
  • Blood Proteins / pharmacology
  • Cell Line
  • Cyclic AMP Response Element-Binding Protein / chemistry
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Cyclic AMP Response Element-Binding Protein / pharmacology*
  • DNA / chemistry
  • DNA / metabolism
  • DNA-Binding Proteins
  • Fungal Proteins / genetics
  • Gene Expression
  • Haplorhini
  • Macromolecular Substances
  • Plasmids
  • Protein Kinases / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae Proteins*
  • Transcription Factors / antagonists & inhibitors*
  • Transcription Factors / genetics
  • Transcription Factors / pharmacology
  • Transcription, Genetic / drug effects

Substances

  • Activating Transcription Factors
  • Blood Proteins
  • Cyclic AMP Response Element-Binding Protein
  • DNA-Binding Proteins
  • Fungal Proteins
  • GAL4 protein, S cerevisiae
  • Macromolecular Substances
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • DNA
  • Protein Kinases