Mitogenic stimulation of quiescent cells results in the expression of new gene products that play a role in monitoring the extracellular environment relative to the progression of cells through the cell cycle. 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 family. Ras proteins and their relatives function as regulatory binary switches in the cell, cycling between active and inactive states. GEM protein is transiently expressed in mid-G1 between 4 and 8 hours after activation. Several lines of evidence suggest that GEM may play a role in signal transduction during G1 progression. The biological role of GEM is being investigated by utilizing constitutively activated (low GTPase activity) or dominant negative forms of GEM.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CB009357-05
Application #
5201027
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Division of Cancer Biology and Diagnosis
Department
Type
DUNS #
City
State
Country
United States
Zip Code