This a revised application to study a novel cDNA that may constitute a fourth subclass of the PLC family, termed PLC-alpha. Based on primary structural features, PLC-alpha is postulated to provide a direct link for regulation between signaling pathways utilizing heterotrimeric G proteins and Ras proteins. The overall goal of this project is to identify the molecular mechanisms by which PLC-alpha is regulated and activates downstream effectors.
The specific aims are: 1) to examine functional and physical interactions between PLC-alpha and heterotrimeric G proteins, using transfection reconstitution approaches; and 2) to examine functional and physical interactions between PLC-alpha and monomeric G proteins, especially those of the Ras family, using transfection and reconstitution approaches. Structural motifs mediating the interactions of PLC-alpha with these regulatory proteins will be also delineated, using truncation and site-directed mutagenesis approaches.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL063407-03
Application #
6537681
Study Section
Pharmacology A Study Section (PHRA)
Program Officer
Rabadan-Diehl, Cristina
Project Start
2000-07-01
Project End
2004-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
3
Fiscal Year
2002
Total Cost
$220,500
Indirect Cost
Name
Northwestern University at Chicago
Department
Pathology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
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Lin, Sun; Sahai, Atul; Chugh, Sumant S et al. (2002) High glucose stimulates synthesis of fibronectin via a novel protein kinase C, Rap1b, and B-Raf signaling pathway. J Biol Chem 277:41725-35