Aragon Anthony D, Rodriguez Angelina L, Meirelles Osorio, Roy Sushmita, Davidson George S, Tapia Phillip H, Allen Chris, Joe Ray, Benn Don, Werner-Washburne Margaret
Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.
Mol Biol Cell. 2008 Mar;19(3):1271-80. doi: 10.1091/mbc.e07-07-0666. Epub 2008 Jan 16.
Cells in glucose-limited Saccharomyces cerevisiae cultures differentiate into quiescent (Q) and nonquiescent (NQ) fractions before entering stationary phase. To understand this differentiation, Q and NQ cells from 101 deletion-mutant strains were tested for viability and reproductive capacity. Eleven mutants that affected one or both phenotypes in Q or NQ fractions were identified. NQ fractions exhibit a high level of petite colonies, and nine mutants affecting this phenotype were identified. Microarray analysis revealed >1300 mRNAs distinguished Q from NQ fractions. Q cell-specific mRNAs encode proteins involved in membrane maintenance, oxidative stress response, and signal transduction. NQ-cell mRNAs, consistent with apoptosis in these cells, encode proteins involved in Ty-element transposition and DNA recombination. More than 2000 protease-released mRNAs were identified only in Q cells, consistent with these cells being physiologically poised to respond to environmental changes. Our results indicate that Q and NQ cells differentiate significantly, with Q cells providing genomic stability and NQ cells providing nutrients to Q cells and a regular source of genetic diversity through mutation and transposition. These studies are relevant to chronological aging, cell cycle, and genome evolution, and they provide insight into complex responses that even simple organisms have to starvation.
在进入稳定期之前,葡萄糖受限的酿酒酵母培养物中的细胞会分化为静止(Q)和非静止(NQ)部分。为了理解这种分化,对来自101个缺失突变株的Q细胞和NQ细胞进行了活力和繁殖能力测试。鉴定出11个影响Q或NQ部分中一种或两种表型的突变体。NQ部分表现出高水平的小菌落,并鉴定出9个影响此表型的突变体。微阵列分析显示,超过1300种mRNA可区分Q细胞和NQ细胞。Q细胞特异性mRNA编码参与膜维持、氧化应激反应和信号转导的蛋白质。与这些细胞中的细胞凋亡一致,NQ细胞mRNA编码参与Ty元件转座和DNA重组的蛋白质。仅在Q细胞中鉴定出2000多种蛋白酶释放的mRNA,这与这些细胞在生理上准备好应对环境变化一致。我们的结果表明,Q细胞和NQ细胞有显著分化,Q细胞提供基因组稳定性,NQ细胞为Q细胞提供营养,并通过突变和转座提供常规的遗传多样性来源。这些研究与时序衰老、细胞周期和基因组进化相关,它们为即使是简单生物体对饥饿的复杂反应提供了见解。