Described herein are plans for establishment of The Alliance for Cellular Signaling-a large-scale (multi-disciplinary and multi-institutional) collaborative effort to understand G protein-regulated and related cellular signaling systems, qualitatively and quantitatively. The Alliance will study signaling in two murine cellular systems: the cardiac myocyte and the B lymphocyte. The experimental efforts of the Alliance will be carried out in its own laboratories (rather than those of its Participating Investigators) under the direction of two System Committees. These laboratories will conduct research on a scale that is larger than practical in individual laboratories and/or that is too specialized for most individuals. However, the experimental plan is also designed to foster and catalyze conventionally-funded research in laboratories through the entire signaling research community and to leverage these efforts for the overall goals. We will also organize a large membership to assemble an informational database, whose core elements will be molecule pages describing the properties and interactions of hundreds of relevant signaling molecules. Bridging projects will be utilized for development of technology A Steering Committee will oversee all aspects of this effort. The experimental efforts of the Alliance will be directed at (1) identification and localization of all relevant molecules in the cells of interest, (2) documentation of the physical and functional interactions of these molecules with each other, (3) quantification of information flow through the signaling systems, and (4) representation of the entire system as a set of interacting processing modules that can be modeled mathematically. The Alliance has promulgated a Policy on Intellectual Property that has been accepted by most participants; we expect all to conform eventually.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Resource-Related Research Projects (R24)
Project #
1R24GM061503-01
Application #
6144551
Study Section
Special Emphasis Panel (ZGM1-BT-1 (01))
Program Officer
Long, Rochelle M
Project Start
1999-12-15
Project End
2000-01-31
Budget Start
1999-12-15
Budget End
2000-01-31
Support Year
1
Fiscal Year
2000
Total Cost
$39,000
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Pharmacology
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Weinmann, A S; Bartley, S M; Zhang, T et al. (2001) Use of chromatin immunoprecipitation to clone novel E2F target promoters. Mol Cell Biol 21:6820-32