Affiliation:
1. Université de Bordeaux and Centre National de la Recherche Scientifique, Institut de Biochimie et Génétique Cellulaires, UMR 5095, F-33000 Bordeaux, France
Abstract
Quiescence is defined as a temporary arrest of proliferation, yet it likely encompasses various cellular situations. Our knowledge about this widespread cellular state remains limited. In particular, little is known about the molecular determinants that orchestrate quiescence establishment and exit. Here we show that upon carbon source exhaustion, budding yeast can enter quiescence from all cell cycle phases. Moreover, using cellular structures that are candidate markers for quiescence, we found that the first steps of quiescence exit can be triggered independently of cell growth and proliferation by the sole addition of glucose in both Saccharomyces cerevisiae and Schizosaccharomyces pombe. Importantly, glucose needs to be internalized and catabolized all the way down to glycolysis to mobilize quiescent cell specific structures, but, strikingly, ATP replenishment is apparently not the key signal. Altogether, these findings strongly suggest that quiescence entry and exit primarily rely on cellular metabolic status and can be uncoupled from the cell cycle.
Publisher
Rockefeller University Press
Reference39 articles.
1. Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures;Allen;J. Cell Biol.,2006
2. Characterization of differentiated quiescent and nonquiescent cells in yeast stationary-phase cultures;Aragon;Mol. Biol. Cell.,2008
3. Protein synthesis requirements for nuclear division, cytokinesis, and cell separation in Saccharomyces cerevisiae;Burke;Mol. Cell. Biol.,1991
4. A new description of cellular quiescence;Coller;PLoS Biol.,2006
5. Reappraisal of serum starvation, the restriction point, G0, and G1 phase arrest points;Cooper;FASEB J.,2003