Despite considerable effort and characterization, the precise role of PKA in regulating sperm development arid the acquisition ofmotility and fertilization competence remains unclear. A major roadblock in these studies has been the lack of techniques tomanipulate the expression and activity of PKA in sperm cells since no readily accessible cell culture model is available that allowsgenetic intervention. This proposal continues our efforts to apply mouse genetic approaches to modify the subunits of PKA andaddress questions that relate to the importance of subcellular localization, PKA activation state, and developmental changes insubunit isoforms.
The specific aims of our proposal include: (1) Analyze the role of S-AKAP84/D-AKAP1 in the development andsurvival of spermatids (2) Determine the role of C subunit during spermatogenesis (3) Examine the anchoring of Rl and itsphysiological significance during spermatogenesis (4) Identify specific PKA substrates in sperm and develop a mechanism toinhibit sperm PKA In vivo. These studies are relevant to larger questions concerning the treatment of infertility and the developmentof male-specific contraceptive approaches.

Project Start
2008-04-01
Project End
2011-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
29
Fiscal Year
2008
Total Cost
$214,667
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Roth, M Y; Amory, J K (2011) Pharmacologic development of male hormonal contraceptive agents. Clin Pharmacol Ther 89:133-6

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