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« Previous AbstractHost acceptance and discrimination byComperia merceti (Compere) (Hymenoptera: Encyrtidae) and evidence for an optimal density range for resource utilization    Next AbstractMechanical stress impairs pheromone signaling via Pkc1-mediated regulation of the MAPK scaffold Ste5 »

Nat Cell Biol


Title:MAP kinase dynamics in response to pheromones in budding yeast
Author(s):Van Drogen F; Stucke VM; Jorritsma G; Peter M;
Address:"Swiss Institute for Experimental Cancer Research (ISREC), Chemin des Boveresses 155, 1066 Epalinges/VD, Switzerland"
Journal Title:Nat Cell Biol
Year:2001
Volume:3
Issue:12
Page Number:1051 - 1059
DOI: 10.1038/ncb1201-1051
ISSN/ISBN:1465-7392 (Print) 1465-7392 (Linking)
Abstract:"Although scaffolding is a major regulator of mitogen-activated protein kinase (MAPK) pathways, scaffolding proteins are poorly understood. During yeast mating, MAPK Fus3p is phosphorylated by MAPKK Ste7p, which is activated by MAPKKK Ste11p. This MAPK module interacts with the scaffold molecule Ste5p. Here we show that Ste11p and Ste7p were predominantly cytoplasmic proteins, while Ste5p and Fus3p were found in the nucleus and the cytoplasm. Ste5p, Ste7p and Fus3p also localized to tips of mating projections in pheromone-treated cells. Using fluorescence recovery after photobleaching (FRAP), we demonstrate that Fus3p rapidly shuttles between the nucleus and the cytoplasm independently of pheromones, Fus3p phosphorylation and Ste5p. Membrane-bound Ste5p can specifically recruit Fus3p and Ste7p to the cell cortex. Ste5p remains stably bound at the plasma membrane, unlike activated Fus3p, which dissociates from Ste5p and translocates to the nucleus"
Keywords:"*Adaptor Proteins, Signal Transducing *Carrier Proteins Cell Membrane/metabolism Cell Nucleus/metabolism Cytoplasm/metabolism Enzyme Activation/drug effects/physiology Fungal Proteins/metabolism Green Fluorescent Proteins Indicators and Reagents/metabolis;"
Notes:"Medlinevan Drogen, F Stucke, V M Jorritsma, G Peter, M eng Research Support, Non-U.S. Gov't England 2002/01/10 Nat Cell Biol. 2001 Dec; 3(12):1051-9. doi: 10.1038/ncb1201-1051"

 
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