The SRC-3/AIB1 coactivator is degraded in a ubiquitin- and ATP-independent manner by the REGgamma proteasome

Cell. 2006 Jan 27;124(2):381-92. doi: 10.1016/j.cell.2005.11.037.

Abstract

Steroid receptor coactivator-3 (SRC-3/AIB1) is an oncogene frequently amplified and overexpressed in breast cancers. Here we report that SRC-3 interacts with REGgamma, a proteasome activator known to stimulate the trypsin-like activity of the 20S proteasome. RNAi knockdown and gain-of-function experiments suggest that REGgamma promotes SRC-3 protein degradation. Cellular levels of REGgamma expression affect estrogen-receptor target-gene expression and cell growth as a result of its ability to promote degradation of the SRC-3 protein. In vitro proteasome proteolysis assays using purified REGgamma, SRC-3, and the 20S proteasome reinforce these conclusions and demonstrate that REGgamma promotes the degradation of SRC-3 in a ubiquitin- and ATP-independent manner. This work demonstrates the first example of a physiologically relevant endogenous cellular target for the REGgamma-proteasome complex. It also highlights the fact that an alternative mode of proteasome-mediated protein degradation, independent of the 19S proteasome regulatory cap, targets the SRC-3 protein for degradation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetyltransferases / drug effects
  • Acetyltransferases / metabolism*
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Autoantigens / metabolism*
  • Autoantigens / pharmacology
  • Cell Enlargement / drug effects
  • Cell Line, Tumor
  • Female
  • Gene Expression Regulation / drug effects
  • HeLa Cells
  • Histone Acetyltransferases
  • Humans
  • Nuclear Receptor Coactivator 3
  • Oncogene Proteins / drug effects
  • Oncogene Proteins / metabolism*
  • Proteasome Endopeptidase Complex / metabolism*
  • Proteasome Endopeptidase Complex / pharmacology
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Trans-Activators / drug effects
  • Trans-Activators / metabolism*
  • Ubiquitin / metabolism*
  • Up-Regulation

Substances

  • Autoantigens
  • Ki antigen
  • Oncogene Proteins
  • Receptors, Estrogen
  • Trans-Activators
  • Ubiquitin
  • Adenosine Triphosphate
  • Acetyltransferases
  • Histone Acetyltransferases
  • NCOA3 protein, human
  • Nuclear Receptor Coactivator 3
  • Proteasome Endopeptidase Complex