Voitenleitner C, Fanning E, Nasheuer H P
Institut für Biochemie, LMU München, Germany.
Oncogene. 1997 Apr 3;14(13):1611-5. doi: 10.1038/sj.onc.1200975.
DNA polymerase alpha-primase is the only known eukaryotic enzyme that can start DNA replication de novo. In this study, we investigated the regulation of DNA replication by phosphorylation of DNA polymerase alpha-primase. The p180 and the p68 subunits of DNA polymerase alpha-primase were phosphorylated using Cyclin A-, B- and E- dependent kinases. This phosphorylation did not influence its DNA polymerase activity on activated DNA, but slightly stimulated primase activity using poly(dT) single-stranded DNA (ssDNA) without changing the product length of primers. In contrast, site-specific initiation of replication on plasmid DNA containing the SV40 origin is affected: Cyclin A-Cdk2 and Cyclin A-Cdc2 inhibited initiation of SV40 DNA replication in vitro, Cyclin B-Cdc2 had no effect and Cyclin E-Cdk2 stimulated the initiation reaction. DNA polymerase alpha-primase that was pre-phosphorylated by Cyclin A-Cdk2 was completely unable to initiate the SV40 DNA replication in vitro; Cyclin B-Cdc2-phosphorylated enzyme was moderately inhibited, while Cyclin E-Cdk2-treated DNA polymerase alpha-primase remained fully active in the initiation reaction.
DNA聚合酶α-引发酶是唯一已知的能够从头起始DNA复制的真核酶。在本研究中,我们研究了通过DNA聚合酶α-引发酶磷酸化对DNA复制的调控。利用细胞周期蛋白A、B和E依赖性激酶对DNA聚合酶α-引发酶的p180和p68亚基进行磷酸化。这种磷酸化不影响其对活化DNA的DNA聚合酶活性,但使用聚(dT)单链DNA(ssDNA)时能轻微刺激引发酶活性,且不改变引物的产物长度。相反,在含有SV40复制起点的质粒DNA上的位点特异性复制起始受到影响:细胞周期蛋白A-Cdk2和细胞周期蛋白A-Cdc2在体外抑制SV40 DNA复制的起始,细胞周期蛋白B-Cdc2无作用,而细胞周期蛋白E-Cdk2刺激起始反应。经细胞周期蛋白A-Cdk2预磷酸化的DNA聚合酶α-引发酶在体外完全无法起始SV40 DNA复制;经细胞周期蛋白B-Cdc2磷酸化的酶受到中度抑制,而经细胞周期蛋白E-Cdk2处理的DNA聚合酶α-引发酶在起始反应中仍保持完全活性。