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Contribution of DNA polymerase delta to DNA replication in permeable CHO cells synchronized in S phase.

机译:在S期同步化的可渗透CHO细胞中DNA聚合酶δ对DNA复制的贡献。

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摘要

To evaluate the relative contributions of DNA polymerase alpha and DNA polymerase delta in chromosome replication during the S phase of the cell cycle, we have used the permeable cell system for replication as a functional assay. We carried out the analysis of DNA polymerases both in quiescent cells stimulated to proliferate and progress through the cell cycle (monolayers) and in actively growing cells separated into progressive stages of the cell cycle by centrifugal elutriation (suspension cultures). DNA polymerase alpha was measured by using the inhibitor butylphenyl dGTP at low concentrations. Using several inhibitors such as aphidicolin, ddTTP and butylphenyl dGTP, we found that DNA polymerase alpha and delta activity were coordinately increased during S phase and declined at the end. However, DNA polymerase delta was performing about 80% of the total replication and DNA polymerase alpha performed only 20%. This high ratio of DNA polymerase delta to DNA polymerase alpha replication activity was maintained throughout S phase in two entirely different experimental approaches.
机译:为了评估DNA聚合酶α和DNA聚合酶δ在细胞周期S期染色体复制中的相对贡献,我们将渗透性细胞系统复制用作功能测定。我们进行了DNA聚合酶的分析,包括在受激激的静止细胞中增殖并在整个细胞周期中前进(单层),以及在通过离心淘析(悬浮培养)分离为细胞周期进行性阶段的活跃生长的细胞中。通过使用低浓度的抑制剂丁基苯基dGTP测量DNA聚合酶α。使用几种抑制剂,如两性霉素,ddTTP和丁基苯基dGTP,我们发现DNA聚合酶的α和δ活性在S期中协同增加,而在末期下降。但是,DNA聚合酶δ占复制总量的80%,而DNA聚合酶α仅占复制的20%。在两种完全不同的实验方法中,整个S期都保持了DNA聚合酶δ与DNA聚合酶α复制活性的高比率。

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