We describe plans for establishment of The Alliance for Cellular Signaling - a large-scale (multidisciplinary 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 cells from the mouse: the cardiac myocyte and the B lymphocyte. Most of 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 of the Alliance is designed to foster and catalyze conventionally funded research in laboratories throughout the entire signaling research community and thereby to leverage these efforts for the overall goals of the Alliance. We will also organize a large membership to assemble an informational database, whose core elements will be Molecule Pages that describe the properties and interactions of hundreds of relevant signaling molecules. Bridging Projects will be utilized for development and application of critical technologies. 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 all participants. All data from Alliance Laboratories will be placed in the public domain by dissemination on the Internet. Funding for the Alliance will be sought from a consortium of major pharmaceutical companies, in addition to this response to RFA GM-99- 007.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
3U54GM062114-03S1
Application #
6655363
Study Section
Special Emphasis Panel (ZGM1 (01))
Program Officer
Long, Rochelle M
Project Start
2000-09-01
Project End
2005-08-31
Budget Start
2002-09-01
Budget End
2003-08-31
Support Year
3
Fiscal Year
2002
Total Cost
$1,574,900
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Stefan, Eduard; Malleshaiah, Mohan K; Breton, Billy et al. (2011) PKA regulatory subunits mediate synergy among conserved G-protein-coupled receptor cascades. Nat Commun 2:598
Rebres, Robert A; Roach, Tamara I A; Fraser, Iain D C et al. (2011) Synergistic Ca2+ responses by G{alpha}i- and G{alpha}q-coupled G-protein-coupled receptors require a single PLC{beta} isoform that is sensitive to both G{beta}{gamma} and G{alpha}q. J Biol Chem 286:942-51
Callender, Hannah L; Horn, Mary Ann; DeCamp, Dianne L et al. (2010) Modeling species-specific diacylglycerol dynamics in the RAW 264.7 macrophage. J Theor Biol 262:679-90
Rebres, Robert A; Moon, Christina; Decamp, Dianne et al. (2010) Clostridium difficile toxin B differentially affects GPCR-stimulated Ca2+ responses in macrophages: independent roles for Rho and PLA2. J Leukoc Biol 87:1041-57
Bao, Xiaoyan Robert; Fraser, Iain D C; Wall, Estelle A et al. (2010) Variability in G-protein-coupled signaling studied with microfluidic devices. Biophys J 99:2414-22
Wall, Estelle A; Zavzavadjian, Joelle R; Chang, Mi Sook et al. (2009) Suppression of LPS-induced TNF-alpha production in macrophages by cAMP is mediated by PKA-AKAP95-p105. Sci Signal 2:ra28
N'Diaye, Elsa-Noah; Branda, Catherine S; Branda, Steven S et al. (2009) TREM-2 (triggering receptor expressed on myeloid cells 2) is a phagocytic receptor for bacteria. J Cell Biol 184:215-23
Hsueh, Robert C; Natarajan, Madhusudan; Fraser, Iain et al. (2009) Deciphering signaling outcomes from a system of complex networks. Sci Signal 2:ra22
Maurya, M R; Bornheimer, S J; Venkatasubramanian, V et al. (2009) Mixed-integer nonlinear optimisation approach to coarse-graining biochemical networks. IET Syst Biol 3:24-39
Jiang, Lily I; Collins, Julie; Davis, Richard et al. (2008) Regulation of cAMP responses by the G12/13 pathway converges on adenylyl cyclase VII. J Biol Chem 283:23429-39

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