Suppr超能文献

细胞周期蛋白A依赖性激酶对DNA聚合酶α-引发酶的磷酸化作用在体外调节DNA复制的起始。

Phosphorylation of DNA polymerase alpha-primase by cyclin A-dependent kinases regulates initiation of DNA replication in vitro.

作者信息

Voitenleitner C, Fanning E, Nasheuer H P

机构信息

Institut für Biochemie, LMU München, Germany.

出版信息

Oncogene. 1997 Apr 3;14(13):1611-5. doi: 10.1038/sj.onc.1200975.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验