The long term objective of this proposal is to identify the biochemical steps which transduce the initial signal of sperm-egg fusion into the various responses of the egg to fertilization. It is now established that egg activation involves the action of protein tyrosine kineses (PTKs) which function to regulate pronuclear migration and fusion, initiation of DNA synthesis, and mitosis. In addition, recent studies have demonstrated that protein tyrosine kinase activity plays a unique and essential role in the fertilized egg to program developmental events at the gastrula stage. The objective of this proposal is to identify those processes in the egg that are regulated by the fertilization induced activation of Fyn kinase activity and to determine the mechanism by which they are controlled. Using the sea urchin egg as a model system, the PI proposes that Fyn kinase functions downstream of the initial signal for egg activation, acting to regulate one or more specific PTK-dependent functions which may include pronuclear migration, DNA synthesis, and mitosis.
Specific aim I will characterize the egg isoform of Fyn kinase and study its expression in the egg. The role of Fyn kinase in egg activation will be determined through microinjection experiments using recombinant GST fusion proteins encoding the unique SH2 and SH3 domains of Fyn N-terminal as specific inhibitors of Fyn function. The hypothesis that Fyn stimulates DNA synthesis via RAS activation will be tested.
Specific aim II will identify the protein substrates of Fyn kinase in the egg. This will allow the PI to establish the specific biochemical pathways that are activated in response to Fyn activity.
Specific Aim III will study the mechanism by which Fyn kinase activity is stimulated at fertilization. Particular emphasis will be placed on the effect of other protein kinases and phosphatases in regulating Fyn catalytic activity.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD014846-19
Application #
6138748
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Tasca, Richard J
Project Start
1997-01-01
Project End
2001-06-30
Budget Start
2000-01-01
Budget End
2001-06-30
Support Year
19
Fiscal Year
2000
Total Cost
$168,939
Indirect Cost
Name
University of Kansas
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Luo, Jinping; Gupta, Vijayalaxmi; Kern, Brian et al. (2012) Role of FYN kinase in spermatogenesis: defects characteristic of Fyn-null sperm in mice. Biol Reprod 86:1-8
Jasti, Susmita; Warren, Bryce D; McGinnis, Lynda K et al. (2012) The autoimmune regulator prevents premature reproductive senescence in female mice. Biol Reprod 86:110
McGinnis, Lynda K; Hong, Xiaoman; Christenson, Lane K et al. (2011) Fer tyrosine kinase is required for germinal vesicle breakdown and meiosis-I in mouse oocytes. Mol Reprod Dev 78:33-47
McGinnis, Lynda K; Carroll, David J; Kinsey, William H (2011) Protein tyrosine kinase signaling during oocyte maturation and fertilization. Mol Reprod Dev 78:831-45
Luo, Jinping; McGinnis, Lynda K; Kinsey, William H (2010) Role of Fyn kinase in oocyte developmental potential. Reprod Fertil Dev 22:966-76
Luo, Jinping; McGinnis, Lynda K; Kinsey, William H (2009) Fyn kinase activity is required for normal organization and functional polarity of the mouse oocyte cortex. Mol Reprod Dev 76:819-31
Kinsey, William H (2009) Analysis of signaling pathways in zebrafish development by microinjection. Methods Mol Biol 518:67-76
McGinnis, Lynda K; Kinsey, William H; Albertini, David F (2009) Functions of Fyn kinase in the completion of meiosis in mouse oocytes. Dev Biol 327:280-7
Sharma, Dipika; Kinsey, William H (2008) Regionalized calcium signaling in zebrafish fertilization. Int J Dev Biol 52:561-70
McGinnis, Lynda K; Albertini, David F; Kinsey, William H (2007) Localized activation of Src-family protein kinases in the mouse egg. Dev Biol 306:241-54

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