Ras regulates assembly of mitogenic signalling complexes through the effector protein IMP.
The signal transduction cascade comprising Raf, mitogen-activated protein (MAP) kinase kinase (MEK) and MAP kinase is a Ras effector pathway that mediates diverse cellular responses to environmental cues and contributes to Ras-dependent oncogenic transformation. Here we report that the Ras effector protein Impedes Mitogenic signal Propagation (IMP) modulates sensitivity of ... the MAP kinase cascade to stimulus-dependent activation by limiting functional assembly of the core enzymatic components through the inactivation of KSR, a scaffold/adaptor protein that couples activated Raf to its substrate MEK. IMP is a Ras-responsive E3 ubiquitin ligase that, on activation of Ras, is modified by auto-polyubiquitination, which releases the inhibition of Raf-MEK complex formation. Thus, Ras activates the MAP kinase cascade through simultaneous dual effector interactions: induction of Raf kinase activity and derepression of Raf-MEK complex formation. IMP depletion results in increased stimulus-dependent MEK activation without alterations in the timing or duration of the response. These observations suggest that IMP functions as a threshold modulator, controlling sensitivity of the cascade to stimulus and providing a mechanism to allow adaptive behaviour of the cascade in chronic or complex signalling environments.
Mesh Terms:
Animals, Cell Line, Enzyme Activation, Humans, MAP Kinase Signaling System, Mice, Mitogen-Activated Protein Kinase Kinases, Molecular Sequence Data, Protein Binding, Protein Kinases, Proto-Oncogene Proteins c-raf, Rats, Ubiquitin, Ubiquitin-Protein Ligases, Xenopus Proteins, Xenopus laevis, ras Proteins
Animals, Cell Line, Enzyme Activation, Humans, MAP Kinase Signaling System, Mice, Mitogen-Activated Protein Kinase Kinases, Molecular Sequence Data, Protein Binding, Protein Kinases, Proto-Oncogene Proteins c-raf, Rats, Ubiquitin, Ubiquitin-Protein Ligases, Xenopus Proteins, Xenopus laevis, ras Proteins
Nature
Date: Jan. 15, 2004
PubMed ID: 14724641
View in: Pubmed Google Scholar
Download Curated Data For This Publication
140494
Switch View:
- Interactions 3