Rouse J, Jackson S P
Wellcome Trust and Cancer Research Campaign, Institute of Cancer and Developmental Biology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK.
EMBO J. 2000 Nov 1;19(21):5801-12. doi: 10.1093/emboj/19.21.5801.
We identified YDR499W as a Saccharomyces cerevisiae open reading frame with homology to several checkpoint proteins, including S. cerevisiae Rfc5p and Schizosaccharomyces pombe Rad26. Disruption of YDR499W (termed LCD1) results in lethality that is rescued by increasing cellular deoxyribonucleotide levels. Cells lacking LCD1 are very sensitive to a range of DNA-damaging agents, including UV irradiation, and to the inhibition of DNA replication. LCD1 is necessary for the phosphorylation and activation of Rad53p in response to DNA damage or DNA replication blocks, and for Chk1p activation in response to DNA damage. LCD1 is also required for efficient DNA damage-induced phosphorylation of Rad9p and for the association of Rad9p with the FHA2 domain of Rad53p after DNA damage. In addition, cells lacking LCD1 are completely defective in the G(1)/S and G(2)/M DNA damage checkpoints. Finally, we reveal that endogenous Mec1p co-immunoprecipitates with Lcd1p both before and after treatment with DNA-damaging agents. These results indicate that Lcd1p is a pivotal checkpoint regulator, involved in both the essential and checkpoint functions of the Mec1p pathway.
我们将YDR499W鉴定为酿酒酵母的一个开放阅读框,它与几种检查点蛋白具有同源性,包括酿酒酵母的Rfc5p和粟酒裂殖酵母的Rad26。YDR499W(称为LCD1)的缺失会导致致死性,而增加细胞脱氧核糖核苷酸水平可挽救这种致死性。缺乏LCD1的细胞对一系列DNA损伤剂(包括紫外线照射)以及DNA复制抑制非常敏感。LCD1对于响应DNA损伤或DNA复制阻滞时Rad53p的磷酸化和激活以及响应DNA损伤时Chk1p的激活是必需的。LCD1对于DNA损伤诱导的Rad9p高效磷酸化以及DNA损伤后Rad9p与Rad53p的FHA2结构域的结合也是必需的。此外,缺乏LCD1的细胞在G(1)/S和G(2)/M DNA损伤检查点中完全存在缺陷。最后,我们发现内源性Mec1p在DNA损伤剂处理前后均与Lcd1p进行共免疫沉淀。这些结果表明Lcd1p是一个关键的检查点调节因子,参与Mec1p途径的基本功能和检查点功能。