S-phase-specific activation of Cds1 kinase defines a subpathway of the checkpoint response in Schizosaccharomyces pombe

被引:333
作者
Lindsay, HD
Griffiths, DJF
Edwards, RJ
Christensen, PU
Murray, JM
Osman, F
Walworth, N
Carr, AM [1 ]
机构
[1] Univ Sussex, MRC, Cell Mutat Unit, Falmer BN1 9RR, Sussex, England
[2] Univ Sussex, Sch Biol Sci, Falmer BN1 9SQ, England
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Piscataway, NJ 08854 USA
[4] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
基金
英国惠康基金;
关键词
Cds1; kinase; S-phase arrest; DNA structure checkpoints; S-pombe;
D O I
10.1101/gad.12.3.382
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Checkpoints that respond to DNA structure changes were originally defined by the inability of yeast mutants to prevent mitosis following DNA damage or S-phase arrest. Genetic analysis has subsequently identified subpathways of the DNA structure checkpoints, including the reversible arrest of DNA synthesis. Here, we show that the Cds1 kinase is required to slow S phase in the presence of DNA-damaging agents. Cds1 is phosphorylated and activated by S-phase arrest and activated by DNA damage during S phase, but not during G(1) or G(2). Activation of Cds1 during S phase is dependent on all six checkpoint Rad proteins, and Cds1 interacts both genetically and physically with Rad26. Unlike its Saccharomyces cerevisiae counterpart Rad53, Cds1 is not required for the mitotic arrest checkpoints and, thus, defines an S-phase specific subpathway of the checkpoint response. We propose a model for the DNA structure checkpoints that offers a ne tv perspective on the function of the DNA structure checkpoint proteins. This model suggests that an intrinsic mechanism linking S phase and mitosis may function independently of the known checkpoint proteins.
引用
收藏
页码:382 / 395
页数:14
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