Deregulation of the G1/S-phase transition is the proximal cause of mortality in old yeast mother cells

被引:29
作者
Neurohr, Gabriel E. [1 ]
Terry, Rachel L. [2 ]
Sandikci, Arzu [1 ]
Zou, Ke [3 ]
Li, Hao [3 ]
Amon, Angelika [1 ,2 ]
机构
[1] MIT, Howard Hughes Med Inst, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
aging; cell cycle; extrachromosomal rDNA circles; G1/S transition; LIFE-SPAN; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTORS; DAMAGED PROTEINS; GENE-EXPRESSION; G1; CYCLINS; REPLICATION; AGE; VERSATILE; SWI4;
D O I
10.1101/gad.312140.118
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Budding yeast cells produce a finite number of daughter cells before they die. Why old yeast cells stop dividing and die is unclear. We found that age-induced accumulation of the G1/S-phase inhibitor Whi5 and defects in G1/S cyclin transcription cause cell cycle delays and genomic instability that result in cell death. We further identified extrachromosomal rDNA (ribosomal DNA) circles (ERCs) to cause the G1/S cyclin expression defect in old cells. Spontaneous segregation of Whi5 and ERCs into daughter cells rejuvenates old mothers, but daughters that inherit these aging factors die rapidly. Our results identify deregulation of the G1/S-phase transition as the proximal cause of age-induced proliferation decline and cell death in budding yeast.
引用
收藏
页码:1075 / 1084
页数:10
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