Williams J I, Cleaver J E
Biochim Biophys Acta. 1979 May 24;562(3):429-37. doi: 10.1016/0005-2787(79)90106-0.
The induction and removal of sites sensitive to T4 endonuclease V from ultraviolet-irradiated Simian Virus 40 (SV40) Form I (supercoiled) DNA during a lytic infection of monkey CV-1 cells was investigated by agarose tube gel electrophoresis. Endonuclease-sensitive sites were induced at a rate of 0.049 sites/SV40 genome per J/m2, or 1.4 sites/1 . 10(8) daltons of DNA per J/m2. This value is similar to the yield of endonuclease-sensitive sites and pyrimidine dimers in uninfected host CV-1 cell DNA. Removal of endonuclease-sensitive sites was dose dependent and non-linear for at least 24 h after irradiation. These results suggest that SV40 DNA is subject to the excision repair mechanisms of the host cell, and that the excision of pyrimidine dimers may be one of the biochemical events underlying host cell reactivation.
通过琼脂糖管凝胶电泳研究了在猴CV - 1细胞的裂解感染过程中,从紫外线照射的猴病毒40(SV40)I型(超螺旋)DNA诱导和去除对T4内切核酸酶V敏感的位点。内切核酸酶敏感位点的诱导速率为每J/m² 0.049个位点/SV40基因组,或每J/m² 1.4个位点/1.1×10⁸道尔顿的DNA。该值与未感染的宿主CV - 1细胞DNA中内切核酸酶敏感位点和嘧啶二聚体的产量相似。照射后至少24小时,内切核酸酶敏感位点的去除是剂量依赖性的且呈非线性。这些结果表明SV40 DNA受到宿主细胞的切除修复机制的影响,并且嘧啶二聚体的切除可能是宿主细胞再激活背后的生化事件之一。