Zou L, Mitchell J, Stillman B
Cold Spring Harbor Laboratory, New York 11724, USA.
Mol Cell Biol. 1997 Feb;17(2):553-63. doi: 10.1128/MCB.17.2.553.
The CDC45 gene of Saccharomyces cerevisiae was isolated by complementation of the cold-sensitive cdc45-1 mutant and shown to be essential for cell viability. Although CDC45 genetically interacts with a group of MCM genes (CDC46, CDC47, and CDC54), the predicted sequence of its protein product reveals no significant sequence similarity to any known Mcm family member. Further genetic characterization of the cdc45-1 mutant demonstrated that it is synthetically lethal with orc2-1, mcm2-1, and mcm3-1. These results not only reveal a functional connection between the origin recognition complex (ORC) and Cdc45p but also extend the CDC45-MCM genetic interaction to all known MCM family members that were shown to be involved in replication initiation. Initiation of DNA replication in cdc45-1 cells was defective, causing a delayed entry into S phase at the nonpermissive temperature, as well as a high plasmid loss rate which could be suppressed by tandem copies of replication origins. Furthermore, two-dimensional gels directly showed that chromosomal origins fired less frequently in cdc45-1 cells at the nonpermissive temperature. These findings suggest that Cdc45p, ORC, and Mcm proteins act in concert for replication initiation throughout the genome.
通过对温度敏感型cdc45-1突变体进行互补,分离出了酿酒酵母的CDC45基因,结果表明该基因对细胞活力至关重要。尽管CDC45在遗传学上与一组MCM基因(CDC46、CDC47和CDC54)相互作用,但其蛋白质产物的预测序列与任何已知的Mcm家族成员均无明显的序列相似性。对cdc45-1突变体的进一步遗传学特征分析表明,它与orc2-1、mcm2-1和mcm3-1存在合成致死性。这些结果不仅揭示了起始识别复合物(ORC)与Cdc45p之间的功能联系,还将CDC45-MCM遗传相互作用扩展到了所有已知的参与复制起始的MCM家族成员。在cdc45-1细胞中,DNA复制起始存在缺陷,导致在非允许温度下进入S期延迟,以及质粒丢失率很高,而串联的复制起点拷贝可以抑制这种情况。此外,二维凝胶直接显示,在非允许温度下,cdc45-1细胞中染色体起点的激发频率较低。这些发现表明,Cdc45p、ORC和Mcm蛋白协同作用,负责整个基因组的复制起始。