Prostate Cell-Specific Regulation of Androgen Receptor Phosphorylation In Vivo

Abstract

We propose that AR phosphorylation at serines 213 and 650 regulate differential target gene expression and recruitment to gene promoters via altered interaction with other cellular transcription factors. To test this hypothesis we have conducted yeast two-hybrid analysis with the N-terminus of wild type AR as well as AR S213A and AR S213E variants. Our preliminary analysis indicates that the screen is preferentially isolating proteins with a known role in gene transcription and we are currently assessing the phosphorylation-dependence of the putative AR interacting proteins. Additionally, we have generated PC3 cells stably transfected with wild type, S650A and S650E AR. We have shown that the cells activate endogenous target genes in response to androgens and are currently investigating classes of genes affected by differential AR phosphorylation. Further, we have optimized conditions to isolate pools of hyper- and hypo-phosphorylated AR in order to isolate proteins that interact with AR in a phosphorylation-dependent manner. These proteins will be identified via mass spectrometry.

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Document Details

Document Type
Technical Report
Publication Date
Nov 01, 2007
Accession Number
ADA482292

Entities

People

  • Samir S. Taneja

Organizations

  • New York University

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Androgen Receptors
  • Androgens
  • Antibodies
  • Cell Line
  • Cells
  • Gene Expression
  • Inhibitors
  • Molecules
  • New York
  • Phosphorylation
  • Prostate
  • Prostate Cancer
  • Proteins
  • Regulations
  • Spectrometry
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Molecular Genetics
  • Prostate Cancer Biology.