Ras signalling on the endoplasmic reticulum and the Golgi
- 2 April 2002
- journal article
- research article
- Published by Springer Nature in Nature Cell Biology
- Vol. 4 (5) , 343-350
- https://doi.org/10.1038/ncb783
Abstract
Current models evoke the plasma membrane (PM) as the exclusive platform from which Ras regulates signalling. We developed a fluorescent probe that reports where and when Ras is activated in living cells. We show that oncogenic H-Ras and N-Ras engage Raf-1 on the Golgi and that endogenous Ras and unpalmitoylated H-Ras are activated in response to mitogens on the Golgi and endoplasmic reticulum (ER), respectively. We also demonstrate that H-Ras that is restricted to the ER can activate the Erk pathway and transform fibroblasts, and that Ras localized on different membrane compartments differentially engages various signalling pathways. Thus, Ras signalling is not limited to the PM, but also proceeds on the endomembrane.Keywords
This publication has 36 references indexed in Scilit:
- Endocytosis and mitogenic signalingCurrent Opinion in Cell Biology, 1999
- Endomembrane Trafficking of RasCell, 1999
- Endoplasmic reticulum membrane localization of Rce1p and Ste24p, yeast proteases involved in carboxyl-terminal CAAX protein processing and amino-terminal a-factor cleavageProceedings of the National Academy of Sciences, 1998
- Control of EGF Receptor Signaling by Clathrin-Mediated EndocytosisScience, 1996
- Activation of Raf as a Result of Recruitment to the Plasma MembraneScience, 1994
- Requirement for Ras in Raf activation is overcome by targeting Raf to the plasma membraneNature, 1994
- The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signalingCell, 1992
- PROTEIN ISOPRENYLATION AND METHYLATION AT CARBOXYL-TERMINAL CYSTEINE RESIDUESAnnual Review of Biochemistry, 1992
- A polybasic domain or palmitoylation is required in addition to the CAAX motif to localize p21ras to the plasma membraneCell, 1990
- Localization of the src gene product of the Harvey strain of MSV to plasma membrane of transformed cells by electron microscopic immunocytochemistryCell, 1980