Growth-dependent signals drive an increase in early G1 cyclin concentration to link cell cycle entry with cell growth

被引:0
作者
Sommer, Robert A. [1 ]
DeWitt, Jerry T. [1 ]
Tan, Raymond [1 ]
Kellogg, Douglas R. [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
来源
ELIFE | 2021年 / 10卷
基金
美国国家卫生研究院;
关键词
Cln3; cell size; Whi5; cell growth; cell cycle; SGK; S; cerevisiae; SACCHAROMYCES-CEREVISIAE; PLASMA-MEMBRANE; SIZE CONTROL; CLN3-CDC28; KINASE; SURFACE GROWTH; BUDDING-YEAST; PROTEINS; DIVISION; CLN3; GENE;
D O I
10.7554/eLife.64364; 10.7554/eLife.64364.sa1; 10.7554/eLife.64364.sa2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Entry into the cell cycle occurs only when sufficient growth has occurred. In budding yeast, the cyclin Cln3 is thought to initiate cell cycle entry by inactivating a transcriptional repressor called Whi5. Growth-dependent changes in the concentrations of Cln3 or Whi5 have been proposed to link cell cycle entry to cell growth. However, there are conflicting reports regarding the behavior and roles of Cln3 and Whi5. Here, we found no evidence that changes in the concentration of Whi5 play a major role in controlling cell cycle entry. Rather, the data suggest that cell growth triggers cell cycle entry by driving an increase in the concentration of Cln3. We further found that accumulation of Cln3 is dependent upon homologs of mammalian SGK kinases that control cell growth and size. Together, the data are consistent with models in which Cln3 is a crucial link between cell growth and the cell cycle.
引用
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页数:28
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