Quiescence is the most common and, arguably, most poorly understood cell cycle state. This is in part because pure populations of quiescent cells are typically difficult to isolate. We report the isolation and characterization of quiescent and nonquiescent cells from stationary-phase (SP) yeast cultures by density-gradient centrifugation. Quiescent cells are dense, unbudded daughter cells formed after glucose exhaustion. They synchronously reenter the mitotic cell cycle, suggesting that they are in a G0 state. Nonquiescent cells are less dense, heterogeneous, and composed of replicatively older, asynchronous cells that rapidly lose the ability to reproduce. Microscopic and flow cytometric analysis revealed that nonquiescent cells accumulate more reactive oxygen species than quiescent cells, and over 21 d, about half exhibit signs of apoptosis and necrosis. The ability to isolate both quiescent and nonquiescent yeast cells from SP cultures provides a novel, tractable experimental system for studies of quiescence, chronological and replicative aging, apoptosis, and the cell cycle.
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3 July 2006
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July 03 2006
Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures
Sabrina Büttner,
Sabrina Büttner
4Institute of Molecular Biology, Biochemistry, and Microbiology, Karl-Franzens University, 8010 Graz, Austria
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Anthony D. Aragon,
Anthony D. Aragon
1Department of Biology
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Osorio Meirelles,
Osorio Meirelles
2Department of Mathematics and Statistics,
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Stephanie W. Ruby,
Stephanie W. Ruby
3Department of Molecular Genetics and Microbiology, Health Sciences Center, University of New Mexico, Albuquerque, NM 87131
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Marten Veenhuis,
Marten Veenhuis
5Department of Eukaryotic Microbiology, University of Groningen, Kerklaan 30, 9750 AA Haren, Netherlands
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Frank Madeo,
Frank Madeo
4Institute of Molecular Biology, Biochemistry, and Microbiology, Karl-Franzens University, 8010 Graz, Austria
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Margaret Werner-Washburne
Margaret Werner-Washburne
1Department of Biology
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Chris Allen
1Department of Biology
Sabrina Büttner
4Institute of Molecular Biology, Biochemistry, and Microbiology, Karl-Franzens University, 8010 Graz, Austria
Anthony D. Aragon
1Department of Biology
Jason A. Thomas
1Department of Biology
Osorio Meirelles
2Department of Mathematics and Statistics,
Jason E. Jaetao
1Department of Biology
Don Benn
1Department of Biology
Stephanie W. Ruby
3Department of Molecular Genetics and Microbiology, Health Sciences Center, University of New Mexico, Albuquerque, NM 87131
Marten Veenhuis
5Department of Eukaryotic Microbiology, University of Groningen, Kerklaan 30, 9750 AA Haren, Netherlands
Frank Madeo
4Institute of Molecular Biology, Biochemistry, and Microbiology, Karl-Franzens University, 8010 Graz, Austria
Margaret Werner-Washburne
1Department of Biology
Correspondence to Margaret Werner-Washburne: [email protected]
Abbreviations used in this paper: AnnV, Annexin V; ANOVA, analysis of variance; DHE, dihydroethidium; FUN-1, 2-chloro-4-(2,3-dihydro-3-methyl-[benzo-1, 3-thiazol-2-yl]-methylidene)-1-phenylquinolinium iodide; PI, propidium iodide; ROS, reactive oxygen species; SP, stationary phase.
Received:
April 17 2006
Accepted:
May 30 2006
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2006
J Cell Biol (2006) 174 (1): 89–100.
Article history
Received:
April 17 2006
Accepted:
May 30 2006
Citation
Chris Allen, Sabrina Büttner, Anthony D. Aragon, Jason A. Thomas, Osorio Meirelles, Jason E. Jaetao, Don Benn, Stephanie W. Ruby, Marten Veenhuis, Frank Madeo, Margaret Werner-Washburne; Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures . J Cell Biol 3 July 2006; 174 (1): 89–100. doi: https://doi.org/10.1083/jcb.200604072
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