Sclafani R A, Fangman W L
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5821-5. doi: 10.1073/pnas.81.18.5821.
The herpes simplex virus type 1 thymidine kinase gene TK complements the defect in five temperature-sensitive mutants and in vitro constructed insertion and deletion mutants of the CDC8 gene of Saccharomyces cerevisiae. The herpes thymidine kinase enzyme acts as both a thymidine kinase and a thymidylate kinase (dTMP kinase). The latter activity is responsible for the cdc8 complementation since all thermosensitive cdc8 mutants are deficient in dTMP kinase activity at all temperatures. However, an intragenic revertant, cdc8-320, which was selected by demanding mitotic growth at the restrictive temperature, exhibits thermolabile dTMP kinase activity. We conclude that CDC8 is the structural gene for dTMP kinase, which catalyzes an essential step in DNA precursor biosynthesis. Previously, it has been shown that the DNA replication defect of cdc8 mutants could not be bypassed by the addition of deoxyribonucleoside triphosphates to permeabilized cells. This apparent discrepancy can be explained by hypothesizing a multiprotein yeast DNA replication complex containing the CDC8 protein.
单纯疱疹病毒1型胸苷激酶基因TK可弥补酿酒酵母CDC8基因的五个温度敏感突变体以及体外构建的插入和缺失突变体的缺陷。疱疹胸苷激酶既作为胸苷激酶又作为胸苷酸激酶(dTMP激酶)发挥作用。后一种活性负责cdc8互补,因为所有温度敏感的cdc8突变体在所有温度下dTMP激酶活性均不足。然而,通过在限制温度下要求有丝分裂生长而选择的基因内回复突变体cdc8-320表现出热不稳定的dTMP激酶活性。我们得出结论,CDC8是dTMP激酶的结构基因,它催化DNA前体生物合成中的一个关键步骤。此前已表明,向通透细胞中添加脱氧核糖核苷三磷酸并不能绕过cdc8突变体的DNA复制缺陷。通过假设含有CDC8蛋白的多蛋白酵母DNA复制复合物,可以解释这一明显的差异。