Hiraga Shin-Ichiro, Hagihara-Hayashi Aki, Ohya Tomoko, Sugino Akio
Laboratories for Biomolecular Networks, Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamada-oka, Suita, Osaka 565-0871, Japan.
Genes Cells. 2005 Apr;10(4):297-309. doi: 10.1111/j.1365-2443.2005.00843.x.
Early in eukaryotic cell cycle, a pre-RC is assembled at each replication origin with ORC, Cdc6, Cdt1 and Mcm2-7 proteins to license the origin for use in the subsequent S phase. Licensed origin must then be activated by S-Cdk and Ddk. At the onset of S phase, RPA is loaded on to the ARS in a reaction stimulated by S-Cdk and Ddk, followed by Cdc45-dependent loading of pol alpha, -delta, and -epsilon. This study examines cell cycle-dependent localization of pol alpha, -delta and -epsilon in Saccharomyces cerevisiae using immuno-histochemical and chromatin immuno-precipitation methods. The results show that pol alpha, -delta, or -epsilon localizes on chromatin as punctate foci at all stages of the cell cycle. However, some foci overlap with or are adjacent to foci pulse-labeled with bromodeoxyuridine during S phase, indicating these are replicating foci. DNA microarray analysis localized pol alpha, -delta, and -epsilon to early firing ARSs on yeast chromosome III and VI at the beginning of S phase. These data collectively suggest that bidirectional replication occurs at specific foci in yeast chromosomes and that pol alpha, -delta, and -epsilon localize and function together at multiple replication forks during S phase.
在真核细胞周期早期,前复制复合物(pre-RC)在每个复制起点与起始识别复合物(ORC)、细胞分裂周期蛋白6(Cdc6)、Cdt1和微小染色体维持蛋白2-7(Mcm2-7)组装在一起,为后续S期使用该起点做好许可准备。然后,已许可的起点必须被S期周期蛋白依赖性激酶(S-Cdk)和Dbf4依赖性激酶(Ddk)激活。在S期开始时,复制蛋白A(RPA)在S-Cdk和Ddk刺激的反应中加载到自主复制序列(ARS)上,随后是依赖于Cdc45的DNA聚合酶α、δ和ε的加载。本研究使用免疫组织化学和染色质免疫沉淀方法研究了酿酒酵母中DNA聚合酶α、δ和ε的细胞周期依赖性定位。结果表明,在细胞周期的所有阶段,DNA聚合酶α、δ或ε都以点状病灶的形式定位于染色质上。然而,在S期,一些病灶与用溴脱氧尿苷脉冲标记的病灶重叠或相邻,表明这些是正在复制的病灶。DNA微阵列分析将DNA聚合酶α、δ和ε定位到S期开始时酵母染色体III和VI上早期激活的自主复制序列上。这些数据共同表明,双向复制发生在酵母染色体的特定病灶处,并且在S期,DNA聚合酶α、δ和ε在多个复制叉处共同定位并发挥作用。