Mechanism of Transcriptional Regulation by Androgen Receptor and its Coactivators in the Context of Chromatin

Abstract

Androgens play important roles in the differentiation, development and maintenance of male reproductive functions as well as in the etiology of prostate cancer. The biological effects of androgens are believed to be mediated through the intracellular androgen receptor (AR), which belongs to the nuclear receptor (NR) superfamily of ligand-regulated transcription factors. Like other NRs, the actions of AR are subject to modulation, either positively or negatively, by an increasing number of co-regulatory proteins, termed coactivators or corepressors. Coactivators are believed to function either as bridging factors between receptors and basal transcription machinery to enhance recruitment of the basal transcription machinery and/or as factors that have capacity to actively remodel repressive chromatin. The purpose of this research is to study the mechanism by which coactivators modulate AR activity in chromatin, the physiological template of transcriptional regulation. In this progress report, we report that we have analyzed how SRC family coactivators and p300 modulate AR activity in the context of chromatin using Xenopus oocyte as a model system. We demonstrate that p300 requires both its histone acetyltransferase activity and interaction with SRC family coactivators to stimulate AR activity. By using chromatin immunoprecipitation assay, we demonstrated that R188l-stimulated transcriptional activation by AR is associated with the promoter targeting of multiple cofactors including the SRC-l, p300, SWI/SNF and TRAP Mediator complex. An increased histone acetylation over the promoter region was also observed. This histone acetylation 5 correlated with the recruitment of CBP/p300. Taken together, our data suggest that hormone-dependent activation by AR is associated with two types of chromatin remodeling, histone acetylation and chromatin remodeling induced by SWI/SNF, as well as the recruitment of TRAP/Mediator complex.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2002
Accession Number
ADA410569

Entities

People

  • Jiemin Wong

Organizations

  • Baylor College of Medicine

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Androgen Receptors
  • Anti-Bacterial Agents
  • Cell Line
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Enzyme Inhibitors
  • Eukaryotes
  • Gene Expression
  • Identification
  • Molecular Biology
  • Protein-Protein Interactions
  • Proteins
  • Thyroid Hormones
  • Transcription Factors
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Prostate Cancer Biology.