Owens J C, Detweiler C S, Li J J
Department of Microbiology and Immunology, University of California, San Francisco, CA 94143-0414, USA.
Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12521-6. doi: 10.1073/pnas.94.23.12521.
The initiation of DNA replication in Saccharomyces cerevisiae requires the protein product of the CDC45 gene. We report that although Cdc45p is present at essentially constant levels throughout the cell cycle, it completes its initiation function in late G1, after START and prior to DNA synthesis. Shortly after mitosis, cells prepare for initiation by assembling prereplicative complexes at their replication origins. These complexes are then triggered at the onset of S phase to commence DNA replication. Cells defective for CDC45 are incapable of activating the complexes to initiate DNA replication. In addition, Cdc45p and Cdc7p/Dbf4p, a kinase implicated in the G1/S phase transition, are dependent on one another for function. These data indicate that CDC45 functions in late G1 phase in concert with CDC7/DBF4 to trigger initiation at replication origins after the assembly of the prereplicative complexes.
酿酒酵母中DNA复制的起始需要CDC45基因的蛋白质产物。我们报告称,尽管Cdc45p在整个细胞周期中基本保持恒定水平,但它在G1晚期、START之后和DNA合成之前完成其起始功能。有丝分裂后不久,细胞通过在其复制起点组装前复制复合物来为起始做准备。然后这些复合物在S期开始时被触发以开始DNA复制。CDC45有缺陷的细胞无法激活这些复合物来起始DNA复制。此外,Cdc45p和Cdc7p/Dbf4p(一种与G1/S期转换有关的激酶)在功能上相互依赖。这些数据表明,CDC45在G1晚期与CDC7/DBF4协同作用,在预复制复合物组装后触发复制起点的起始。