Proliferation/Quiescence: When to start? Where to stop? What to stock?

Cell Division

Volumn 6, Issue , 2011, Pages

  Daignan Fornier, Bertrand ^a,b   Sagot, Isabelle ^a,b  

^a UNIVERSITÉ DE BORDEAUX   (France)

^b CNRS   (France)

Author keywords

Cell cycle; Metabolism; Quiescence; Restriction point; Saccharomyces cerevisiae; Start point; Starvation

Indexed keywords

PROKARYOTA; SACCHAROMYCES CEREVISIAE;

EID: 83055168285     PISSN: None     EISSN: 17471028     Source Type: Journal    
DOI: 10.1186/1747-1028-6-20     Document Type: Note

References (41)

1. Pardee AB. A restriction point for control of normal animal cell proliferation. Proc Natl Acad Sci USA 1974, 71:1286-1290. 10.1073/pnas.71.4.1286, 388211, 4524638.
2. Hereford LM, Hartwell LH. Sequential gene function in the initiation of Saccharomyces cerevisiae DNA synthesis. J Mol Biol 1974, 84:445-461. 10.1016/0022-2836(74)90451-3, 4618856.
3. Hartwell LH, Culotti J, Pringle JR, Reid BJ. Genetic control of the cell division cycle in yeast. Science 1974, 183:46-51. 10.1126/science.183.4120.46, 4587263.
4. Davidson GS, Joe RM, Roy S, Meirelles O, Allen CP, Wilson MR, Tapia PH, Manzanilla EE, Dodson AE, Chakraborty S, et al. The proteomics of quiescent and nonquiescent cell differentiation in yeast stationary-phase cultures. Mol Biol Cell 2011, 22:988-998. 10.1091/mbc.E10-06-0499, 3069023, 21289090.
5. Gresham D, Boer VM, Caudy A, Ziv N, Brandt NJ, Storey JD, Botstein D. System-level analysis of genes and functions affecting survival during nutrient starvation in Saccharomyces cerevisiae. Genetics 2011, 187:299-317. 10.1534/genetics.110.120766, 3018308, 20944018.
6. Klosinska MM, Crutchfield CA, Bradley PH, Rabinowitz JD, Broach JR. Yeast cells can access distinct quiescent states. Genes Dev 2011, 25:336-349. 10.1101/gad.2011311, 3042157, 21289062.
7. Laporte D, Lebaudy A, Sahin A, Pinson B, Ceschin J, Daignan-Fornier B, Sagot I. Metabolic status rather than cell cycle signals control quiescence entry and exit. J Cell Biol 2011, 192:949-957. 10.1083/jcb.201009028, 3063145, 21402786.
8. Daignan-Fornier B, Sagot I. Proliferation/quiescence: the controversial "aller-retour". Cell Div 2011, 6:10. 10.1186/1747-1028-6-10, 3113920, 21554667.
9. Charvin G, Oikonomou C, Siggia ED, Cross FR. Origin of irreversibility of cell cycle start in budding yeast. PLoS Biol 2010, 8:e1000284. 10.1371/journal.pbio.1000284, 2797597, 20087409.
10. Skotheim JM, Di Talia S, Siggia ED, Cross FR. Positive feedback of G1 cyclins ensures coherent cell cycle entry. Nature 2008, 454:291-296. 10.1038/nature07118, 2606905, 18633409.
11. Cooper S. Reappraisal of serum starvation, the restriction point, G0, and G1 phase arrest points. Faseb J 2003, 17:333-340. 10.1096/fj.02-0352rev, 12631573.
12. Cooper S. On the proposal of a G0 phase and the restriction point. Faseb J 1998, 12:367-373.
13. Wei W, Nurse P, Broek D. Yeast cells can enter a quiescent state through G1, S, G2, or M phase of the cell cycle. Cancer Res 1993, 53:1867-1870.
14. Drewinko B, Yang LY, Barlogie B, Trujillo JM. Cultured human tumour cells may be arrested in all stages of the cycle during stationary phase: demonstration of quiescent cells in G1, S and G2 phase. Cell Tissue Kinet 1984, 17:453-463.
15. Baisch H. Different quiescence states of three culture cell lines detected by acridine orange staining of cellular RNA. Cytometry 1988, 9:325-331. 10.1002/cyto.990090409, 2456898.
16. Coudreuse D, Nurse P. Driving the cell cycle with a minimal CDK control network. Nature 2011, 468:1074-1079.
17. Tzur A, Kafri R, LeBleu VS, Lahav G, Kirschner MW. Cell growth and size homeostasis in proliferating animal cells. Science 2009, 325:167-171. 10.1126/science.1174294, 2905160, 19589995.
18. Goranov AI, Cook M, Ricicova M, Ben-Ari G, Gonzalez C, Hansen C, Tyers M, Amon A. The rate of cell growth is governed by cell cycle stage. Genes Dev 2009, 23:1408-1422. 10.1101/gad.1777309, 2701574, 19528319.
19. Goranov AI, Amon A. Growth and division--not a one-way road. Curr Opin Cell Biol 2010, 22:795-800. 10.1016/j.ceb.2010.06.004, 2988085, 20667436.
20. Hartwell LH, Unger MW. Unequal division in Saccharomyces cerevisiae and its implications for the control of cell division. J Cell Biol 1977, 75:422-435. 10.1083/jcb.75.2.422, 2109951, 400873.
21. Johnston GC, Pringle JR, Hartwell LH. Coordination of growth with cell division in the yeast Saccharomyces cerevisiae. Exp Cell Res 1977, 105:79-98. 10.1016/0014-4827(77)90154-9, 320023.
22. Popolo L, Vanoni M, Alberghina L. Control of the yeast cell cycle by protein synthesis. Exp Cell Res 1982, 142:69-78. 10.1016/0014-4827(82)90410-4, 6754401.
23. Slater ML, Sharrow SO, Gart JJ. Cell cycle of Saccharomyces cerevisiae in populations growing at different rates. Proc Natl Acad Sci USA 1977, 74:3850-3854. 10.1073/pnas.74.9.3850, 431757, 333447.
24. Unger MW, Hartwell LH. Control of cell division in Saccharomyces cerevisiae by methionyl-tRNA. Proc Natl Acad Sci USA 1976, 73:1664-1668. 10.1073/pnas.73.5.1664, 430360, 775494.
25. Costello G, Rodgers L, Beach D. Fission yeast enters the stationary phase G0 state from either mitotic G1 or G2. Curr Genet 1986, 11:119-125.
26. Takeo K, Tanaka R, Miyaji M, Nishimura K. Unbudded G2 as well as G1 arrest in the stationary phase of the basidiomycetous yeast Cryptococcus neoformans. FEMS Microbiol Lett 1995, 129:231-235.
27. Cameron IL, Bols NC. Effect of cell population density on G2 arrest in Tetrahymena. J Cell Biol 1975, 67:518-522. 10.1083/jcb.67.3.518, 2111659, 811669.
28. Martinez MJ, Roy S, Archuletta AB, Wentzell PD, Anna-Arriola SS, Rodriguez AL, Aragon AD, Quinones GA, Allen C, Werner-Washburne M. Genomic analysis of stationary-phase and exit in Saccharomyces cerevisiae: gene expression and identification of novel essential genes. Mol Biol Cell 2004, 15:5295-5305. 10.1091/mbc.E03-11-0856, 532011, 15456898.
29. Gasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown PO. Genomic expression programs in the response of yeast cells to environmental changes. Mol Biol Cell 2000, 11:4241-4257. 15070, 11102521.
30. Radonjic M, Andrau JC, Lijnzaad P, Kemmeren P, Kockelkorn TT, van Leenen D, van Berkum NL, Holstege FC. Genome-wide analyses reveal RNA polymerase II located upstream of genes poised for rapid response upon S. cerevisiae stationary phase exit. Mol Cell 2005, 18:171-183. 10.1016/j.molcel.2005.03.010, 15837421.
31. Saldanha AJ, Brauer MJ, Botstein D. Nutritional homeostasis in batch and steady-state culture of yeast. Mol Biol Cell 2004, 15:4089-4104. 10.1091/mbc.E04-04-0306, 515343, 15240820.
32. Wu J, Zhang N, Hayes A, Panoutsopoulou K, Oliver SG. Global analysis of nutrient control of gene expression in Saccharomyces cerevisiae during growth and starvation. Proc Natl Acad Sci USA 2004, 101:3148-3153. 10.1073/pnas.0308321100, 365758, 14973188.
33. Yotsuyanagi Y. [Study of yeast mitochondria. I. Variations in mitochondrial ultrastructure during the aerobic growth cycle.]. J Ultrastruct Res 1962, 7:121-140. 10.1016/S0022-5320(62)80031-8, 14002756.
34. Sagot I, Pinson B, Salin B, Daignan-Fornier B. Actin bodies in yeast quiescent cells: an immediately available actin reserve?. Mol Biol Cell 2006, 17:4645-4655. 10.1091/mbc.E06-04-0282, 1635378, 16914523.
35. Laporte D, Salin B, Daignan-Fornier B, Sagot I. Reversible cytoplasmic localization of the proteasome in quiescent yeast cells. J Cell Biol 2008, 181:737-745. 10.1083/jcb.200711154, 2396804, 18504300.
36. Teixeira D, Sheth U, Valencia-Sanchez MA, Brengues M, Parker R. Processing bodies require RNA for assembly and contain nontranslating mRNAs. Rna 2005, 11:371-382. 10.1261/rna.7258505, 1370727, 15703442.
37. Brengues M, Teixeira D, Parker R. Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science 2005, 310:486-489. 10.1126/science.1115791, 1863069, 16141371.
38. Narayanaswamy R, Levy M, Tsechansky M, Stovall GM, O'Connell JD, Mirrielees J, Ellington AD, Marcotte EM. Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation. Proc Natl Acad Sci USA 2009, 106:10147-10152. 10.1073/pnas.0812771106, 2691686, 19502427.
39. Noree C, Sato BK, Broyer RM, Wilhelm JE. Identification of novel filament-forming proteins in Saccharomyces cerevisiae and Drosophila melanogaster. J Cell Biol 2010, 190:541-551. 10.1083/jcb.201003001, 2928026, 20713603.
40. Tapia H, Morano KA. Hsp90 nuclear accumulation in quiescence is linked to chaperone function and spore development in yeast. Mol Biol Cell 2010, 21:63-72. 10.1091/mbc.E09-05-0376, 2801720, 19889838.
41. Schafer G, McEvoy CR, Patterton HG. The Saccharomyces cerevisiae linker histone Hho1p is essential for chromatin compaction in stationary phase and is displaced by transcription. Proc Natl Acad Sci USA 2008, 105:14838-14843. 10.1073/pnas.0806337105, 2567454, 18799740.