Wold M S, Li J J, Kelly T J
Proc Natl Acad Sci U S A. 1987 Jun;84(11):3643-7. doi: 10.1073/pnas.84.11.3643.
Analysis of the kinetics of simian virus 40 (SV40) DNA replication in vitro demonstrated the existence of a slow presynthesis reaction that occurs prior to onset of extensive chain elongation and is dependent on a subset of the cellular proteins required for the complete replication reaction. When the presynthesis reaction is carried out in the presence of topoisomerase I, it is possible to detect extensive unwinding of the template DNA. This unwinding reaction is specific for templates that contain the wild-type SV40 origin of DNA replication and requires SV40 large tumor antigen (T antigen), ATP, and a protein fraction derived from HeLa cells. The required cellular protein may be a eukaryotic single-stranded-DNA-binding protein (SSB), since unwinding of the template is also observed when Escherichia coli SSB is substituted for the HeLa protein fraction. These observations suggest that during the initial stages of SV40 DNA replication, T antigen binds specifically to the viral origin and locally unwinds the DNA. This origin-dependent unwinding reaction is presumably a prerequisite for subsequent priming and elongation steps.
对猿猴病毒40(SV40)DNA体外复制动力学的分析表明,在广泛的链延伸开始之前存在一个缓慢的合成前反应,该反应依赖于完整复制反应所需的一部分细胞蛋白。当在拓扑异构酶I存在的情况下进行合成前反应时,可以检测到模板DNA的广泛解旋。这种解旋反应对含有野生型SV40 DNA复制起点的模板具有特异性,并且需要SV40大T抗原(T抗原)、ATP和源自HeLa细胞的蛋白质组分。所需的细胞蛋白可能是一种真核单链DNA结合蛋白(SSB),因为当用大肠杆菌SSB替代HeLa蛋白组分时,也能观察到模板的解旋。这些观察结果表明,在SV40 DNA复制的初始阶段,T抗原特异性地结合到病毒起点并局部解开DNA。这种依赖于起点的解旋反应大概是后续引发和延伸步骤的先决条件。