Role of the PY Motif Containing Protein, WBP-2 in ER, PR Signaling and Breast Tumorigenesis

Abstract

Our data demonstrates that WBP-2 is recruited onto the hormone responsive promoters in the presence of hormone and it specifically enhances the transactivation functions of PR and ER. Our data also demonstrates that WBP-2 contains an intrinsic activation domain and the cPPXY of WBP-2 is essential for its coactivation and intrinsic activation functions. Our preliminary data also demonstrates that the WBP-2 binding protein, YAP1 enhances PR and ER transactivation but YAP1 s coactivation function is absolutely dependent on WBP-2. Furthermore, cPPXY motif of WBP-2 and WW-domain of YAP1 is required for YAP1 to work as a transcriptional coactiva-tor. Additionally, our data also indicate that the coactivation functions of WBP-2 and YAP1 are suppressed by WWOX1, suggesting that WWOX1 may regulates the transactivation functions of ER and PR by antagonizing the functions of WBP-2 and YAP1. Taken together our data estab-lished the role of WBP-2 and YAP1 as coactivators and WWOX1 as a repressor for ER and PR transactivation pathways.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2007
Accession Number
ADA469779

Entities

People

  • Sarath C. Dhananjayan
  • Zafar Nawaz

Organizations

  • University of Miami

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Androgen Receptors
  • Biomedical And Dental Materials
  • Breast Cancer
  • Carrier Proteins
  • Cell Physiological Processes
  • Cells
  • Chemical Reactions
  • Chemistry
  • Diseases And Disorders
  • Fungi
  • Genetic Structures
  • Molecular Biology
  • Molecules
  • Proteins
  • Transcription Factors
  • Tumor Cell Line

Fields of Study

  • Computer science

Readers

  • Breast cancer cell signaling and growth regulation.
  • Geochemistry