A transcriptional coactivator, steroid receptor coactivator-3, selectively augments steroid receptor transcriptional activity

J Biol Chem. 1998 Oct 16;273(42):27645-53. doi: 10.1074/jbc.273.42.27645.

Abstract

Estrogen receptors ERalpha and ERbeta are members of the family of nuclear hormone receptors and act as ligand-inducible transcriptional factors, which regulate the expression of target genes on binding to cognate response elements. We report here the characterization of steroid receptor coactivator-3 (SRC-3), a coactivator of nuclear receptor transcription that is a member of a family of steroid receptor coactivators that includes SRC-1 and transcription intermediate factor-2. SRC-3 enhanced ERalpha and progesterone receptor-stimulated gene transcription in a ligand-dependent manner, but stimulation of ERbeta-mediated transcription was not observed. Protein-protein interaction assays, including real-time interaction analyses with BIAcore, demonstrated that the affinity of the ERalpha interaction with SRC-3 was much higher than that observed for the ERbeta interaction with SRC-3. Mutational analysis suggests a potential interplay between the transactivation function-1 and -2 domains of ERalpha and SRC-3. Furthermore, an intrinsic transactivation function was observed in the C-terminal half of SRC-3. Finally, SRC-3 was differentially expressed in various tissues and, among several tumor cells examined, was most abundant in the nuclear fraction of MCF-7 breast cancer cells. Therefore, SRC-3, a third member of a family of steroid receptor coactivators, has a distinct tissue distribution and intriguing selectivity between ERalpha and ERbeta.

MeSH terms

  • Acetyltransferases
  • Biosensing Techniques
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Estrogen Receptor alpha
  • Gene Expression Regulation
  • Histone Acetyltransferases
  • Humans
  • Nuclear Receptor Coactivator 3
  • Oncogene Proteins
  • Protein Binding
  • Receptors, Estrogen / metabolism*
  • Receptors, Progesterone / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Tissue Distribution
  • Trans-Activators / metabolism*
  • Transcription, Genetic*

Substances

  • DNA, Complementary
  • Estrogen Receptor alpha
  • Oncogene Proteins
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Trans-Activators
  • Acetyltransferases
  • Histone Acetyltransferases
  • NCOA3 protein, human
  • Nuclear Receptor Coactivator 3