Estrogen receptor alpha represses transcription of early target genes via p300 and CtBP1

Mol Cell Biol. 2009 Apr;29(7):1749-59. doi: 10.1128/MCB.01476-08. Epub 2009 Feb 2.

Abstract

The regulation of gene expression by nuclear receptors controls the phenotypic properties and diverse biologies of target cells. In breast cancer cells, estrogen receptor alpha (ERalpha) is a master regulator of transcriptional stimulation and repression, yet the mechanisms by which agonist-bound ERalpha elicits repression are poorly understood. We analyzed early estrogen-repressed genes and found that ERalpha is recruited to ERalpha binding sites of these genes, albeit more transiently and less efficiently than for estrogen-stimulated genes. Of multiple cofactors studied, only p300 was recruited to ERalpha binding sites of repressed genes, and its knockdown prevented estrogen-mediated gene repression. Because p300 is involved in transcription initiation, we tested whether ERalpha might be trying to stimulate transcription at repressed genes, with ultimately failure and a shift to a repressive program. We found that estrogen increases transcription in a rapid but transient manner at early estrogen-repressed genes but that this is followed by recruitment of the corepressor CtBP1, a p300-interacting partner that plays an essential role in the repressive process. Thus, at early estrogen-repressed genes, ERalpha initiates transient stimulation of transcription but fails to maintain the transcriptional process observed at estrogen-stimulated genes; rather, it uses p300 to recruit CtBP1-containing complexes, eliciting chromatin modifications that lead to transcriptional repression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation / drug effects
  • Alcohol Oxidoreductases / metabolism*
  • Binding Sites
  • Cell Line, Tumor
  • DNA-Binding Proteins / metabolism*
  • E1A-Associated p300 Protein / metabolism*
  • Estradiol / pharmacology
  • Estrogen Receptor alpha / metabolism*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Histones / metabolism
  • Humans
  • Lysine / metabolism
  • Models, Genetic
  • Protein Binding / drug effects
  • Protein Transport / drug effects
  • RNA, Small Interfering / metabolism
  • Repressor Proteins / metabolism*
  • Time Factors
  • Transcription, Genetic* / drug effects

Substances

  • DNA-Binding Proteins
  • Estrogen Receptor alpha
  • Histones
  • RNA, Small Interfering
  • Repressor Proteins
  • estrogen receptor alpha, human
  • Estradiol
  • Alcohol Oxidoreductases
  • C-terminal binding protein
  • E1A-Associated p300 Protein
  • EP300 protein, human
  • Lysine