Basnakian A, Banfalvi G, Sarkar N
Department of Metabolic Regulation, Boston Biomedical Research Institute, MA 02114.
Nucleic Acids Res. 1989 Jun 26;17(12):4757-67. doi: 10.1093/nar/17.12.4757.
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.
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,我们使用可渗透细胞系统进行复制作为功能检测。我们在刺激增殖并经历细胞周期的静止细胞(单层)以及通过离心淘析分离到细胞周期不同进展阶段的活跃生长细胞(悬浮培养物)中对DNA聚合酶进行了分析。通过使用低浓度的抑制剂丁基苯基dGTP来测量DNA聚合酶α。使用诸如阿非科林、ddTTP和丁基苯基dGTP等几种抑制剂,我们发现DNA聚合酶α和δ的活性在S期协同增加并在末期下降。然而,DNA聚合酶δ进行了约80%的总复制,而DNA聚合酶α仅进行20%。在两种完全不同的实验方法中,整个S期DNA聚合酶δ与DNA聚合酶α复制活性的这一高比例都得以维持。