We have cloned a mitogen-induced gene from T cells, GEM, that encodes a GTP-binding protein that is a novel member of the ras superfamily. GEM protein is transiently expressed in mid-G1 between 4 and 8 hours after activation. Ras proteins and their relatives function as regulatory binary switches in the cell, cycling between active (GTP-bound) and inactive (GDP-bound) states. Several lines of evidence suggest that GEM may play a role in signal transduction during G1 progression or associated with differentiation. In order to identify the signaling pathways in which Gem is involved, we have focused our efforts on identifying proteins which are either upstream regulators or downstream effectors of Gem. We have used the yeast two-hybrid system to identify several proteins which physically interact with Gem, and the characterization of the functional signifcance of these interactions is on-going. 14-3-3 proteins recognize phosphoserine motifs and are thought to act as scaffolding proteins that may stabalize signaling complexes or regulate protein-protein interactions. The binding site of 14-3-3 in the Gem protein has been mapped to two cooperating sites in the carboxy terminus of Gem. There is no evidence that 14-3-3 binding to Gem significantly changes the subcellular localization of Gem. We are testing the hypothesis that 14-3-3 association modulates the protein partners to which Gem binds. An additional protein found to bind Gem in a GTP-dependent manner is ROK (rho kinase). ROK is a major effector protein of Rho which is important in modulating the function of the actin cytoskeleton. Gem inhibited ROK activity in vitro. We are assaying the effect of Gem on several ROCK dependent functions in various cellular contexts. We have found that Gem expression decreases ROK dependent stress fibers and focal adhesions in fibroblasts. In addition, Gem inhibits Rho mediated colony formation in soft agar. Gem also stimulates neurite extension in neuroblastoma cells, an activity that appears to reflect a physiological function of Gem.

Agency
National Institute of Health (NIH)
Institute
Division of Clinical Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC009357-10
Application #
6433394
Study Section
(LP)
Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code