Spatial segregation of Ras signaling - New evidence from fission yeast

被引:18
作者
Chang, Eric C.
Philips, Mark R.
机构
[1] Baylor Coll Med, Dept Mol & Cell Biol, Breast Ctr, Houston, TX 77030 USA
[2] NYU, Sch Med, Dept Med Cell Biol & Pharmacol, New York, NY USA
关键词
signal transduction; oncogene cancer; Rho; GTPase; lipid rafts; S; pombe; Prenylation;
D O I
10.4161/cc.5.17.3187
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Ras GTPases act as binary switches for signal transduction pathways that are important for growth regulation and tumorigenesis. Despite the biochemical simplicity of this switch, Ras proteins control multiple pathways, and the functions of the four mammalian Ras proteins are not overlapping. This raises an important question - how does a Ras protein selectively regulate a particular activity? One recently emerging model suggests that a single Ras protein can control different functions by acting in distinct cellular compartments. A critical test of this model is to identify pathways that are selectively controlled by Ras when it is localized to a particular compartment. A recent study has examined Ras signaling in the fission yeast Schizosaccharomyces pombe, which expresses only one Ras protein that controls two separate evolutionarily conserved pathways. This study demonstrates that whereas Ras localized to the plasma membrane selectively regulates a MAP kinase pathway to mediate mating pheromone signaling, Ras localized to the endomembrane activates a Cdc42 pathway to mediate cell polarity and protein trafficking. This study has provided unambiguous evidence for compartmentalized signaling of Ras.
引用
收藏
页码:1936 / 1939
页数:4
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