Burger H, Doerfler W
J Virol. 1974 May;13(5):975-92. doi: 10.1128/JVI.13.5.975-992.1974.
KB cells productively infected with human adenovirus type 2 contain an alkalistable class of viral DNA sedimenting in a broad zone between 50 and 90S as compared to 34S for virion DNA. This type of DNA is characterized as viral by DNA-DNA hybridization. It is extremely sensitive to shear fragmentation. Extensive control experiments demonstrate that the fast-sedimenting viral DNA is not due to artifactual drag of viral DNA mechanically trapped in cellular DNA or to association of viral DNA with protein or RNA. Furthermore, the fast-sedimenting DNA is found after infection with multiplicities between 1 and 1,000 PFU/cell and from 6 to 8 h postinfection until very late in infection (24 h). Analysis in dye-buoyant density gradients eliminates the possibility that the fast-sedimenting viral DNA represents supercoiled circular molecules. Upon equilibrium centrifugation in alkaline CsCl density gradients, the fast-sedimenting viral DNA bands in a density stratum intermediate between that of cellular and viral DNA. In contrast, the 34S virion DNA isolated and treated in the same manner as the fast-sedimenting DNA cobands with viral marker DNA. After ultrasonic treatment of the fast-sedimenting viral DNA, it shifts to the density positions of viral DNA and to a lesser extent to that of cellular DNA. The evidence presented here demonstrates that the 50 to 90S viral DNA represents adenovirus DNA covalently integrated into cell DNA.
被人腺病毒2型有效感染的KB细胞含有一类对碱稳定的病毒DNA,与病毒粒子DNA的34S相比,其在50至90S的宽区域内沉降。这种DNA通过DNA-DNA杂交被鉴定为病毒DNA。它对剪切断裂极其敏感。大量对照实验表明,快速沉降的病毒DNA不是由于机械捕获在细胞DNA中的病毒DNA的人为拖曳,也不是由于病毒DNA与蛋白质或RNA的结合。此外,在感染复数为1至1000 PFU/细胞且在感染后6至8小时直至感染后期(24小时)后发现快速沉降的DNA。在染料浮力密度梯度中的分析排除了快速沉降的病毒DNA代表超螺旋环状分子的可能性。在碱性CsCl密度梯度中进行平衡离心时,快速沉降的病毒DNA在细胞DNA和病毒DNA之间的密度层中形成条带。相比之下,以与快速沉降DNA相同的方式分离和处理的34S病毒粒子DNA与病毒标记DNA共形成条带。对快速沉降的病毒DNA进行超声处理后,它转移到病毒DNA的密度位置,并在较小程度上转移到细胞DNA的密度位置。此处提供的证据表明,50至90S的病毒DNA代表共价整合到细胞DNA中的腺病毒DNA。