Varmus H E, Guntaka R V, Deng C T, Bishop J M
Cold Spring Harb Symp Quant Biol. 1975;39 Pt 2:987-96. doi: 10.1101/sqb.1974.039.01.113.
We have reviewed our recent evidence for the following scheme for synthesis and integration of viral DAN after infection of permissive cells by ASV: Within the first 3 hours of infection, duplex, virus-specific DNA the length of a subunit of the viral genome (3 times 10(6) daltons) is synthesized in the cytoplasm of infected cells by a virion-associated DNA polymerase; viral DNA probably forms a covalently closed circular duplex prior to integration into host nuclear DNA. Integration and the usual consequences of viral infection can be inhibited by ethidium bromide. We have described a number of features of viral DNA prior to its integration and have indicated how these features can be exploited in the purification of viral DNA. Viral DNA has also been measured in nonpermissive (mammalian) cells in which the variable expression of viral genes is controlled by unknown mechanisms.
我们已回顾了近期关于劳氏肉瘤病毒(ASV)感染允许性细胞后病毒DNA合成与整合的如下机制的证据:在感染的最初3小时内,感染细胞的细胞质中,病毒体相关的DNA聚合酶合成了双链的、病毒特异性的DNA,其长度为病毒基因组一个亚基的长度(3×10⁶道尔顿);病毒DNA在整合入宿主核DNA之前可能形成共价闭合环状双链。溴化乙锭可抑制整合及病毒感染的常见后果。我们已描述了病毒DNA整合前的一些特征,并指出了如何利用这些特征来纯化病毒DNA。在非允许性(哺乳动物)细胞中也检测到了病毒DNA,在这些细胞中,病毒基因的可变表达受未知机制控制。