4.8 Article

Compartmentalized signaling of Ras in fission yeast

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0603318103

Keywords

cancer; Cdc42; Int6; mitogen-activated protein kinase; eIF3

Funding

  1. NCI NIH HHS [CA107187, CA116034, R01 CA116034, R01 CA090464, R01 CA107187, CA118495, R01 CA118495, CA90464] Funding Source: Medline
  2. NCRR NIH HHS [RR00592, P41 RR000592] Funding Source: Medline
  3. NIGMS NIH HHS [GM55279, R01 GM055279] Funding Source: Medline

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Compartment-specific Ras signaling is an emerging paradigm that may explain the multiplex outputs from a single GTPase. The fission yeast, Schizosaccharomyces pombe, affords a simple system in which to study Ras signaling because it has a single Ras protein, Ras1, that regulates two distinct pathways: one that controls mating through a Byr2-mitogen-activated protein kinase cascade and one that signals through Scd1-Cdc42 to maintain elongated cell morphology. We generated Ras1 mutants that are restricted to either the endomembrane or the plasma membrane. Protein binding studies showed that each could interact with the effectors of both pathways However, when examined in ras1 null cells, endomembrane-restricted Ras1 supported morphology but not mating, and, conversely, plasma membrane-restricted Ras1 supported mating but did not signal to Scd1-Cdc42. These observations provide a striking demonstration of compartment-specific Ras signaling and indicate that spatial specificity in the Ras pathway is evolutionarily conserved.

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