The 26S proteasome is required for estrogen receptor-alpha and coactivator turnover and for efficient estrogen receptor-alpha transactivation

Mol Cell. 2000 Jun;5(6):939-48. doi: 10.1016/s1097-2765(00)80259-2.

Abstract

Estrogen receptor-alpha (ER alpha) is downregulated in the presence of its cognate ligand, estradiol (E2), through the ubiquitin proteasome pathway. Here, we show that ubiquitin proteasome function is required for ER alpha to serve as a transcriptional activator. Deletion of the last 61 amino acids of ER alpha, including residues that form helix 12, abolishes ligand-mediated downregulation of the receptor as do point mutations in the ligand binding domain that impair coactivator binding. In addition, coactivators also are subject to degradation by the 26S proteasome, but their intrinsic transcriptional activity is not affected. These data provide evidence that protein interactions with ER alpha coactivator binding surfaces are important for ligand-mediated receptor down-regulation and suggest that receptor and coactivator turnover contributes to ER alpha transcriptional activity.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Cysteine Proteinase Inhibitors / pharmacology
  • Down-Regulation / drug effects
  • Estradiol / metabolism
  • Estradiol / pharmacology
  • Estrogen Receptor alpha
  • Humans
  • Leupeptins / pharmacology
  • Ligands
  • Ligases / antagonists & inhibitors
  • Ligases / metabolism
  • Molecular Sequence Data
  • Mutation
  • Peptide Hydrolases / metabolism*
  • Proteasome Endopeptidase Complex*
  • Protein Binding
  • Receptors, Estrogen / chemistry
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Sequence Alignment
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcriptional Activation* / drug effects
  • Transfection
  • Tumor Cells, Cultured
  • Ubiquitin-Protein Ligases

Substances

  • Cysteine Proteinase Inhibitors
  • Estrogen Receptor alpha
  • Leupeptins
  • Ligands
  • Receptors, Estrogen
  • Trans-Activators
  • Estradiol
  • Ubiquitin-Protein Ligases
  • Peptide Hydrolases
  • Proteasome Endopeptidase Complex
  • ATP dependent 26S protease
  • Ligases
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde