Steroid hormone receptors, among them the human androgen receptor, are maintained in an inactive state prior to hormone binding by association with hsp90 and other molecular chaperons. The studies proposed by Dr. Caplan will focus on the role of the molecular chaperon Ydj1p in this process, a DnaJ homolog that functions together with Hsp70 in protein assembly and disassembly events. Previous biochemical studies indicated that Hsp70 plays a direct role in the assembly of Hsp90 with the glucocorticoid receptor in a process requiring ATP, and a similar role of Ydj1p has been confirmed by genetic studies in vivo. Studies are proposed which will use a combination of genetic and biochemical approaches to dissect this process with a view to understanding the role of Ydj1p in receptor activation. These studies will be performed with yeast cells expressing human androgen receptor.
The specific aims of this proposal are: 1). To define the domains of YDJ1 that function in human androgen receptor activation. 2). To determine where Ydj1p functions in the process of androgen receptor activation, and 3). To characterize how a DnaJ/Hsp70 chaperon pair functions in the activation of the androgen receptor in higher eukaryotes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK049065-02
Application #
2430229
Study Section
Molecular Cytology Study Section (CTY)
Program Officer
Margolis, Ronald N
Project Start
1996-06-01
Project End
2000-05-31
Budget Start
1997-06-01
Budget End
1998-05-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
114400633
City
New York
State
NY
Country
United States
Zip Code
10029
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Caplan, A J (1999) Hsp90's secrets unfold: new insights from structural and functional studies. Trends Cell Biol 9:262-8
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