Ligand-induced transrepression by VDR through association of WSTF with acetylated histones

EMBO J. 2005 Nov 16;24(22):3881-94. doi: 10.1038/sj.emboj.7600853. Epub 2005 Oct 27.


We have previously shown that the novel ATP-dependent chromatin-remodeling complex WINAC is required for the ligand-bound vitamin D receptor (VDR)-mediated transrepression of the 25(OH)D3 1alpha-hydroxylase (1alpha(OH)ase) gene. However, the molecular basis for VDR promoter association, which does not involve its binding to specific DNA sequences, remains unclear. To address this issue, we investigated the function of WSTF in terms of the association between WINAC and chromatin for ligand-induced transrepression by VDR. Results of in vitro experiments using chromatin templates showed that the association of unliganded VDR with the promoter required physical interactions between WSTF and both VDR and acetylated histones prior to VDR association with chromatin. The acetylated histone-interacting region of WSTF was mapped to the bromodomain, and a WSTF mutant lacking the bromodomain served as a dominant-negative mutant in terms of ligand-induced transrepression of the 1alpha(OH)ase gene. Thus, our findings indicate that WINAC associates with chromatin through a physical interaction between the WSTF bromodomain and acetylated his tones, which appears to be indispensable for VDR/promoter association for ligand-induced transrepression of 1alpha(OH)ase gene expression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / genetics
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / metabolism
  • Acetylation
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Chromatin / metabolism
  • Gene Expression Regulation*
  • HeLa Cells
  • Histone Deacetylases / metabolism
  • Histones / chemistry
  • Histones / metabolism*
  • Humans
  • Ligands
  • Macromolecular Substances
  • Mice
  • Models, Genetic
  • Nucleosomes / chemistry
  • Nucleosomes / metabolism
  • Promoter Regions, Genetic
  • Protein Structure, Tertiary
  • RNA Interference
  • Rats
  • Receptors, Calcitriol / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*


  • BAZ1B protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Chromatin
  • Histones
  • Ligands
  • Macromolecular Substances
  • Nucleosomes
  • Receptors, Calcitriol
  • Transcription Factors
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
  • Histone Deacetylases