Bentley N J, Holtzman D A, Flaggs G, Keegan K S, DeMaggio A, Ford J C, Hoekstra M, Carr A M
MRC Cell Mutation Unit, Sussex University, Falmer, UK.
EMBO J. 1996 Dec 2;15(23):6641-51.
The rad3 gene of Schizosaccharomyces pombe is required for checkpoint pathways that respond to DNA damage and replication blocks. We report the complete rad3 gene sequence and show that rad3 is the homologue of Saccharomyces cerevisiae ESR1 (MEC1/SAD3) and Drosophila melanogaster mei-41 checkpoint genes. This establishes Rad3/Mec1 as the only conserved protein which is required for all the DNA structure checkpoints in both yeast model systems. Rad3 is an inessential member of the 'lipid kinase' subclass of kinases which includes the ATM protein defective in ataxia telangiectasia patients. Mutational analysis indicates that the kinase domain is required for Rad3 function, and immunoprecipitation of overexpressed Rad3 demonstrates an associated protein kinase activity. The previous observation that rad3 mutations can be rescued by a truncated clone lacking the kinase domain may be due to intragenic complementation. Consistent with this, biochemical data suggest that Rad3 exists in a complex containing multiple copies of Rad3. We have identified a novel human gene (ATR) whose product is closely related to Rad3/Esr1p/Mei-41. ATR can functionally complement esr1-1 radiation sensitivity in S. cerevisiae. Together, the structural conservation and functional complementation suggest strongly that the mechanisms underlying the DNA structure checkpoints are conserved throughout evolution.
粟酒裂殖酵母的rad3基因是对DNA损伤和复制阻断作出反应的检查点途径所必需的。我们报告了完整的rad3基因序列,并表明rad3是酿酒酵母ESR1(MEC1/SAD3)和黑腹果蝇mei-41检查点基因的同源物。这确立了Rad3/Mec1是酵母模型系统中所有DNA结构检查点所必需的唯一保守蛋白。Rad3是激酶“脂质激酶”亚类中的一个非必需成员,该亚类包括共济失调毛细血管扩张症患者中存在缺陷的ATM蛋白。突变分析表明激酶结构域是Rad3功能所必需的,过表达的Rad3的免疫沉淀显示出相关的蛋白激酶活性。先前观察到rad3突变可被缺乏激酶结构域的截短克隆拯救,这可能是由于基因内互补。与此一致的是,生化数据表明Rad3存在于一个包含多个Rad3拷贝的复合物中。我们鉴定出了一个新的人类基因(ATR),其产物与Rad3/Esr1p/Mei-41密切相关。ATR在功能上可以互补酿酒酵母中esr1-1的辐射敏感性。总之,结构保守性和功能互补性强烈表明DNA结构检查点的潜在机制在整个进化过程中是保守的。