Smale S T, Tjian R
Mol Cell Biol. 1986 Nov;6(11):4077-87. doi: 10.1128/mcb.6.11.4077-4087.1986.
We have combined in vitro DNA replication reactions and immunological techniques to analyze biochemical interactions between simian virus (SV40) large T antigen and components of the cellular replication apparatus. First, in vitro SV40 DNA replication was characterized with specific origin mutants. Next, monoclonal antibodies were used to demonstrate that a specific domain of T antigen formed a complex with cellular DNA polymerase alpha. Several antibodies were identified that coprecipitated T antigen and DNA polymerase alpha, while others were found to selectively prevent this interaction and concomitantly inhibit DNA replication. DNA polymerase alpha also bound efficiently to a T-antigen affinity column, confirming the immunoprecipitation results and providing a useful method for purification of the complete protein complex. Taken together, these results suggest that the T-antigen-polymerase association may be a key step in the initiation of SV40 DNA replication.
我们结合了体外DNA复制反应和免疫学技术,以分析猿猴病毒(SV40)大T抗原与细胞复制装置各组分之间的生化相互作用。首先,利用特定的起始突变体对体外SV40 DNA复制进行了表征。其次,使用单克隆抗体证明T抗原的一个特定结构域与细胞DNA聚合酶α形成了复合物。鉴定出了几种能共沉淀T抗原和DNA聚合酶α的抗体,同时发现其他一些抗体能选择性地阻止这种相互作用并随之抑制DNA复制。DNA聚合酶α也能有效地结合到T抗原亲和柱上,这证实了免疫沉淀结果,并提供了一种纯化完整蛋白质复合物的有用方法。综上所述,这些结果表明T抗原与聚合酶的结合可能是SV40 DNA复制起始的关键步骤。