Ontology highlight
ABSTRACT: Background
Growth factors induce a characteristically short-lived Ras activation in cells emerging from quiescence. Extensive work has shown that transient as opposed to sustained Ras activation is critical for the induction of mitogenic programs. Mitogen-induced accumulation of active Ras-GTP results from increased nucleotide exchange driven by the nucleotide exchange factor Sos. In contrast, the mechanism accounting for signal termination and prompt restoration of basal Ras-GTP levels is unclear, but has been inferred to involve feedback inhibition of Sos. Remarkably, how GTP-hydrolase activating proteins (GAPs) participate in controlling the rise and fall of Ras-GTP levels is unknown.Results
Monitoring nucleotide exchange of Ras in permeabilized cells we find, unexpected
SUBMITTER: Hennig A
PROVIDER: S-EPMC4746934 | biostudies-literature | 2016 Feb
REPOSITORIES: biostudies-literature