Parkhurst J R, Peterson A R, Heidelberger C
Proc Natl Acad Sci U S A. 1973 Nov;70(11):3200-4. doi: 10.1073/pnas.70.11.3200.
Breakdown of HeLa cell DNA begins within 90 min after infection with vaccinia virus at a multiplicity of infection of 2-plaque-forming units per cell, and ends about 7.5 hr after infection. HeLa cell DNA is degraded to a uniform size of 1 to 2 x 10(7) daltons, as judged by alkaline sucrose sedimentation analysis. The rate of host-cell DNA degradation by vaccinia virus increased directly with the multiplicity of infection. Sedimentation patterns in neutral and alkaline sucrose gradients of viral DNA from infected cells, as well as from partially purified virions, indicated that two size classes of DNA were present. Class 1 DNA sediments like T4 DNA in neutral gradients and has a molecular weight twice that of T4 DNA in alkaline gradients. Class II DNA sediments as a molecule of lower molecular weight than T4 DNA in both types of gradients. Infection of prelabeled HeLa cells with vaccinia virus did not result either in formation of trichloroacetic acid-soluble radioactivity or, upon purification of the virions, radioactivity associated with class I DNA, indicating that vaccinia virus does not reutilize HeLa cell DNA.
在每细胞感染复数为2个噬斑形成单位的情况下,用痘苗病毒感染HeLa细胞后90分钟内,HeLa细胞DNA开始降解,并在感染后约7.5小时结束。通过碱性蔗糖沉降分析判断,HeLa细胞DNA被降解为1至2×10⁷道尔顿的均匀大小。痘苗病毒对宿主细胞DNA的降解速率直接随感染复数增加。来自感染细胞以及部分纯化病毒粒子的病毒DNA在中性和碱性蔗糖梯度中的沉降模式表明存在两种大小类别的DNA。第1类DNA在中性梯度中沉降方式类似于T4 DNA,在碱性梯度中分子量是T4 DNA的两倍。第II类DNA在两种梯度中沉降时分子量均低于T4 DNA。用痘苗病毒感染预先标记的HeLa细胞,既未导致三氯乙酸可溶性放射性的形成,在纯化病毒粒子时也未导致与第1类DNA相关的放射性,这表明痘苗病毒不会再利用HeLa细胞DNA。