A vast number of signaling systems have been shown to be regulated by heterotrimeric guanine nucleotide binding regulatory proteins (G proteins). Cellular processes controlled through G protein action including hormone, neurotransmitter and growth factor action, and these proteins have also been implicated in intracellular membrane trafficking and secretion. The broad goal of the research proposed in this application is to understand the molecular mechanisms of how specific members of the G protein family function in specific cellular signaling pathways. The proposed research centers on elucidating the signaling pathway(s) controlled by one such member, termed GZ. GZ is a G protein predominately found in neuroendocrine tissues that has been linked, among other things, to control of cyclic nucleotide levels in these tissues. GZ contains unique structural features that result in properties that distinguish it from most other characterized G proteins, including a very slow intrinsic rate of GTP hydrolysis toxin and the capacity to be regulated by direct phosphorylation mediated by protein kinase C. An interaction cloning strategy that has recently been completed has resulted in the identification of four proteins that interact with GZ. Three of the identified GZ-interacting proteins can be directly implicated in cellular signaling processes, while the fourth is the product of a recently-identified gene homologous to a Drosophila gene whose function is unknown but which has been implicated in eye development in this organism. We will employ a variety of biochemical, molecular, and cellular techniques to study these four proteins in a concerted effort to ascertain the functional consequences of their interaction with GZ and to elucidate potential involvement in GZ- mediated signaling processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM055717-03
Application #
6386685
Study Section
Pharmacology A Study Section (PHRA)
Program Officer
Cole, Alison E
Project Start
1999-05-01
Project End
2003-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
3
Fiscal Year
2001
Total Cost
$233,955
Indirect Cost
Name
Duke University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
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Nixon, Andrew B; Casey, Patrick J (2004) Analysis of the regulation of microtubule dynamics by interaction of RGSZ1 (RGS20) with the neuronal stathmin, SCG10. Methods Enzymol 390:53-64
Nixon, Andrew B; Grenningloh, Gabriele; Casey, Patrick J (2002) The interaction of RGSZ1 with SCG10 attenuates the ability of SCG10 to promote microtubule disassembly. J Biol Chem 277:18127-33
Burgon, P G; Lee, W L; Nixon, A B et al. (2001) Phosphorylation and nuclear translocation of a regulator of G protein signaling (RGS10). J Biol Chem 276:32828-34