Shellman Y G, Schauer I E, Oshiro G, Dohrmann P, Sclafani R A
Department of Biochemistry and Molecular Genetics, University of Colorado Health Sciences Center, Denver 80262, USA.
Mol Gen Genet. 1998 Sep;259(4):429-36. doi: 10.1007/s004380050833.
Cdc7/Dbf4 protein kinase is required for the initiation of DNA replication in Saccharomyces cerevisiae. Cdc7/Dbf4 protein kinase is not a cyclin-dependent kinase (CDK), but is regulated in a similar fashion in that the Cdc7 kinase subunit is inactive in the absence of the regulatory subunit Dbf4. In contrast to what is known about CDKs, Cdc7/Dbf4 protein kinase is shown to be an oligomer in the cell in this report. Genetic data that support this claim include interallelic complementation between several cdc7ts alleles and the cdc7T281A allele and also the results of experiments using the two-hybrid system with Cdc7 in both DNA-binding and transactivation domain plasmids. A molecular interaction between two different Cdc7 molecules was shown by using a HA-tagged Cdc7 protein that differs in size from the wild-type Cdc7 protein: an anti-HA antibody immunoprecipitates both proteins in approximately equal stoichiometry. Analysis of the native molecular weight of Cdc7/Dbf4 protein kinase is consistent with oligomerization of the Cdc7 protein in that complexes of about 180 and 300 kDa were found. Oligomers of Cdc7 protein may exist for the purpose of allosteric regulation or to allow phosphorylation of multiple substrate protein molecules.
Cdc7/Dbf4蛋白激酶是酿酒酵母DNA复制起始所必需的。Cdc7/Dbf4蛋白激酶不是细胞周期蛋白依赖性激酶(CDK),但其调节方式类似,即Cdc7激酶亚基在没有调节亚基Dbf4时无活性。与已知的CDK不同,本报告显示Cdc7/Dbf4蛋白激酶在细胞中是一种寡聚体。支持这一说法的遗传学数据包括几个cdc7ts等位基因与cdc7T281A等位基因之间的等位基因互补,以及在DNA结合和反式激活结构域质粒中使用Cdc7的双杂交系统的实验结果。通过使用大小与野生型Cdc7蛋白不同的HA标签Cdc7蛋白,显示了两个不同Cdc7分子之间的分子相互作用:抗HA抗体以大致相等的化学计量比免疫沉淀两种蛋白。对Cdc7/Dbf4蛋白激酶天然分子量的分析与Cdc7蛋白的寡聚化一致,因为发现了约180和300 kDa的复合物。Cdc7蛋白的寡聚体可能是为了变构调节或允许多个底物蛋白分子的磷酸化而存在。