Allen J B, Zhou Z, Siede W, Friedberg E C, Elledge S J
Howard Hughes Medical Institute, Baylor College of Medicine, Houston, Texas 77030.
Genes Dev. 1994 Oct 15;8(20):2401-15. doi: 10.1101/gad.8.20.2401.
Inhibition of DNA synthesis prevents mitotic entry through the action of the S-phase checkpoint. We have isolated S-phase arrest-defective (sad) mutants that show lethality in the presence of the DNA synthesis inhibitor hydroxyurea (HU). Several of these mutants show phenotypes consistent with inappropriate mitotic entry in the presence of unreplicated DNA, indicating a defect in the S-phase checkpoint. sad1 mutants are additionally defective for the G1 and G2 DNA damage checkpoints, and for DNA damage-induced transcription of RNR2 and RNR3. The transcriptional response to DNA damage requires activation of the Dun1 protein kinase. Activation of Dun1 in response to replication blocks or DNA damage is blocked in sad1 mutants. The HU sensitivity of sad1 mutants is suppressed by mutations in CKS1, a subunit of the p34CDC28 kinase, further establishing a link between cell cycle progression and lethality. sad1 mutants are allelic to rad53, a radiation-sensitive mutant. SAD1 encodes an essential protein kinase. The observation that SAD1 controls three distinct checkpoints suggests a common mechanism for cell cycle arrest at these points. Together, these observations implicate protein phosphorylation in the cellular response to DNA damage and replication blocks.
DNA合成的抑制通过S期检查点的作用阻止有丝分裂的进入。我们分离出了S期阻滞缺陷(sad)突变体,这些突变体在DNA合成抑制剂羟基脲(HU)存在的情况下表现出致死性。其中一些突变体表现出的表型与在未复制DNA存在时不适当的有丝分裂进入一致,表明S期检查点存在缺陷。sad1突变体在G1和G2期DNA损伤检查点以及DNA损伤诱导的RNR2和RNR3转录方面也存在缺陷。对DNA损伤的转录反应需要Dun1蛋白激酶的激活。在sad1突变体中,对复制阻滞或DNA损伤的Dun1激活被阻断。p34CDC28激酶亚基CKS1中的突变抑制了sad1突变体对HU的敏感性,进一步确立了细胞周期进程与致死性之间的联系。sad1突变体与辐射敏感突变体rad53等位。SAD1编码一种必需的蛋白激酶。SAD1控制三个不同检查点的观察结果表明在这些点上细胞周期阻滞存在共同机制。这些观察结果共同表明蛋白磷酸化参与了细胞对DNA损伤和复制阻滞的反应。