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Cds1激酶的S期特异性激活定义了粟酒裂殖酵母中检查点反应的一个子途径。

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

作者信息

Lindsay H D, Griffiths D J, Edwards R J, Christensen P U, Murray J M, Osman F, Walworth N, Carr A M

机构信息

Medical Research Council (MRC) Cell Mutation Unit, Sussex University, Falmer, Sussex BN1 9RR, UK.

出版信息

Genes Dev. 1998 Feb 1;12(3):382-95. doi: 10.1101/gad.12.3.382.

Abstract

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 G1 or G2. 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 new 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.

摘要

最初,对DNA结构变化作出反应的检查点是由酵母突变体在DNA损伤或S期停滞之后无法阻止有丝分裂来定义的。随后的遗传学分析确定了DNA结构检查点的子途径,包括DNA合成的可逆停滞。在此,我们表明,在存在DNA损伤剂的情况下,Cds1激酶是减缓S期所必需的。Cds1在S期停滞时被磷酸化并激活,在S期被DNA损伤激活,但在G1或G2期则不然。S期Cds1的激活依赖于所有六种检查点Rad蛋白,并且Cds1在遗传和物理上都与Rad26相互作用。与酿酒酵母中的对应物Rad53不同,有丝分裂停滞检查点不需要Cds1,因此,它定义了检查点反应的一个S期特异性子途径。我们提出了一个DNA结构检查点模型,该模型为DNA结构检查点蛋白的功能提供了新的视角。该模型表明,连接S期和有丝分裂的内在机制可能独立于已知的检查点蛋白发挥作用。

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