Burgers P M
Department of Biological Chemistry, Washington University School of Medicine, St. Louis, MO 63110.
Nucleic Acids Res. 1988 Jul 25;16(14A):6297-307. doi: 10.1093/nar/16.14.6297.
Human cyclin/PCNA (proliferating cell nuclear antigen) is structurally, functionally, and immunologically homologous to the calf thymus auxiliary protein for DNA polymerase delta. This auxiliary protein has been investigated as a stimulatory factor for the nuclear DNA polymerases from S. cerevisiae. Calf cyclin/PCNA enhances by more than ten-fold the ability of DNA polymerase III to replicate templates with high template/primer ratios, e.g. poly(dA).oligo(dT) (40:1). The degree of stimulation increases with the template/primer ratio. At a high template/primer ratio, i.e. low primer density, cyclin/PCNA greatly increases processive DNA synthesis by DNA polymerase III. At low template/primer ratios (e.g. poly(dA).oligo(dT) (2.5:1), where addition of cyclin/PCNA only minimally increases the processivity of DNA polymerase III, a several-fold stimulation of total DNA synthesis is still observed. This indicates that cyclin/PCNA may also increase productive binding of DNA polymerase III to the template-primer and stabilize the template-primer-polymerase complex. The activity of yeast DNA polymerases I and II is not affected by addition of cyclin/PCNA. These results strengthen the hypothesis that yeast DNA polymerase III is functionally analogous to the mammalian DNA polymerase delta.
人细胞周期蛋白/增殖细胞核抗原(PCNA)在结构、功能和免疫方面与小牛胸腺DNA聚合酶δ辅助蛋白同源。这种辅助蛋白已被作为酿酒酵母核DNA聚合酶的刺激因子进行研究。小牛细胞周期蛋白/PCNA能使DNA聚合酶III复制高模板/引物比例模板(如聚(dA)·寡聚(dT)(40:1))的能力提高十倍以上。刺激程度随模板/引物比例增加。在高模板/引物比例,即低引物密度下,细胞周期蛋白/PCNA极大地增加了DNA聚合酶III的持续DNA合成。在低模板/引物比例(如聚(dA)·寡聚(dT)(2.5:1))时,添加细胞周期蛋白/PCNA仅略微增加DNA聚合酶III的持续合成能力,但仍能观察到总DNA合成有几倍的刺激作用。这表明细胞周期蛋白/PCNA也可能增加DNA聚合酶III与模板-引物的有效结合,并稳定模板-引物-聚合酶复合物。添加细胞周期蛋白/PCNA不会影响酵母DNA聚合酶I和II的活性。这些结果强化了酵母DNA聚合酶III在功能上类似于哺乳动物DNA聚合酶δ的假说。