Wang H, Elledge S J
Howard Hughes Medical Institute, Verna and Marrs McLean Department of Biochemistry, Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3824-9. doi: 10.1073/pnas.96.7.3824.
In addition to DNA polymerase complexes, DNA replication requires the coordinate action of a series of proteins, including regulators Cdc28/Clb and Dbf4/Cdc7 kinases, Orcs, Mcms, Cdc6, Cdc45, and Dpb11. Of these, Dpb11, an essential BRCT repeat protein, has remained particularly enigmatic. The Schizosaccharomyces pombe homolog of DPB11, cut5, has been implicated in the DNA replication checkpoint as has the POL2 gene with which DPB11 genetically interacts. Here we describe a gene, DRC1, isolated as a dosage suppressor of dpb11-1. DRC1 is an essential cell cycle-regulated gene required for DNA replication. We show that both Dpb11 and Drc1 are required for the S-phase checkpoint, including the proper activation of the Rad53 kinase in response to DNA damage and replication blocks. Dpb11 is the second BRCT-repeat protein shown to control Rad53 function, possibly indicating a general function for this class of proteins. DRC1 and DPB11 show synthetic lethality and reciprocal dosage suppression. The Drc1 and Dpb11 proteins physically associate and function together to coordinate DNA replication and the cell cycle.
除了DNA聚合酶复合物外,DNA复制还需要一系列蛋白质的协同作用,包括调节因子Cdc28/Clb和Dbf4/Cdc7激酶、Orcs、Mcms、Cdc6、Cdc45和Dpb11。其中,Dpb11是一种必需的含BRCT重复序列的蛋白质,其功能一直特别神秘。DPB11在粟酒裂殖酵母中的同源物cut5以及与DPB11存在遗传相互作用的POL2基因都与DNA复制检查点有关。在此,我们描述了一个基因DRC1,它是作为dpb11 - 1的剂量抑制子而分离得到的。DRC1是DNA复制所需的一个必需的细胞周期调控基因。我们发现,S期检查点需要Dpb11和Drc1,包括响应DNA损伤和复制阻滞时Rad53激酶的正确激活。Dpb11是已被证明可控制Rad53功能的第二种含BRCT重复序列的蛋白质,这可能表明这类蛋白质具有普遍功能。DRC1和DPB11表现出合成致死性和相互的剂量抑制作用。Drc1和Dpb11蛋白在物理上相互关联并共同发挥作用,以协调DNA复制和细胞周期。