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First published online 10 February 2009
doi: 10.1242/jcs.042424
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Research Article |
1 Department of Biosciences, University of Kent, Canterbury, Kent CT2 7NJ, UK
2 School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD
3 Department of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK
4 Department of Biotecnologie e Bioscienze University Milano-Bicocca, Piazza della Scienza 2, 20126, Milano, Italy
* Author for correspondence (e-mail: c.w.gourlay{at}kent.ac.uk)
Accepted 3 November 2008
Elucidating the mechanisms by which eukaryotic cells coordinate environmental signals with intracellular `fate' decisions, such as apoptosis, remains one of the important challenges facing cell biologists. It has recently emerged that the dynamic nature of the actin cytoskeleton is an important factor in the linkage of sensation of extracellular stimuli to signalling mechanisms that regulate programmed cell death. In yeast, actin has been shown to play a role in the regulation of apoptosis as cells prepare themselves for quiescence in the face of nutritional exhaustion, by facilitating the shutdown of Ras-cAMP-PKA pathway activity. Here, we demonstrate that the loss of Whi2p function, a protein known to influence cell cycle exit under conditions of nutritional stress, leads to cell death in yeast that displays the hallmarks of actin-mediated apoptosis. We show that actin-mediated apoptosis occurs as a result of inappropriate Ras-cAMP-PKA activity in
whi2 cells. Cells lacking Whi2p function exhibit an aberrant accumulation of activated Ras2 at the mitochondria in response to nutritional depletion. This study provides evidence that the shutdown of cAMP-PKA signalling activity in wild-type cells involves Whi2p-dependent targeting of Ras2p to the vacuole for proteolysis. We also demonstrate for the first time that Whi2p-dependent regulation of cAMP-PKA signalling plays a physiological role in the differentiation of yeast colonies by facilitating elaboration of distinct zones of cell death.
Key words: PKA, ROS, Ras, Actin, Mitochondria, Yeast
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