Shank P R, Hughes S H, Kung H J, Majors J E, Quintrell N, Guntaka R V, Bishop J M, Varmus H E
Cell. 1978 Dec;15(4):1383-95. doi: 10.1016/0092-8674(78)90063-6.
Three major species of viral DNA have been observed in cells infected by retroviruses: a linear, double-stranded copy of a subunit of viral RNA; closed circular DNA; and proviral DNA inserted covalently into the genome of the host cell. We have studied the structures of the unintegrated forms of avian sarcoma virus (ASA) DNA using agarose gel electrophoresis in conjunction with restriction endonucleases and molecular hybridization techniques. The linear duplex DNA is approximately the same length as a subunit of viral RNA (approximately 10 kb) and it bears natural repeats of approximately 300 nucleotides at its termini. The repeats are composed of sequences derived from both the 3' and 5' termini of viral RNA in a manner suggesting that the viral DNA polymerase is transferred twice between templates. Thus the first end begins with a sequence from the 5' terminus of viral RNA and is permuted by about 100 nucleotides with respect to the 3' terminus of viral RNA; the linear DNA terminates with a sequence of about 200 nucleotides derived from the 3' end of viral RNA. We represent this structure, synthesized from right to left, as 3'5'-----3'5'. Two closed circular species of approximately monomeric size have been identified. The less abundant species contain all the sequences identified in linear DNA, including two copies in tandem of the 300 nucleotide 3'5' repeat. The major species lacks about 300 base pairs (bp) mapped to the region of the repeated sequence; thus it presumably contains only a single copy of that sequence. The strategies used to determine these structures involved the assignment of over 20 cleavage sites for restriction endonucleases on the physical maps of ASV DNA. Several strains of ASV were compared with respect to these sites, and the sites have been located in relation to deletions frequently observed in the env and src genes of ASV.
在感染逆转录病毒的细胞中观察到三种主要的病毒DNA类型:病毒RNA一个亚基的线性双链拷贝;闭环DNA;以及共价插入宿主细胞基因组的前病毒DNA。我们使用琼脂糖凝胶电泳结合限制性内切酶和分子杂交技术研究了禽肉瘤病毒(ASA)DNA未整合形式的结构。线性双链DNA的长度与病毒RNA的一个亚基大致相同(约10 kb),其末端带有约300个核苷酸的天然重复序列。这些重复序列由来自病毒RNA 3'和5'末端的序列组成,其方式表明病毒DNA聚合酶在模板之间转移了两次。因此,第一个末端始于病毒RNA 5'末端的序列,相对于病毒RNA的3'末端排列了约100个核苷酸;线性DNA以来自病毒RNA 3'末端的约200个核苷酸的序列终止。我们将这种从右到左合成的结构表示为3'5'-----3'5'。已鉴定出两种大致为单体大小的闭环类型。含量较少的类型包含线性DNA中鉴定出的所有序列,包括300个核苷酸3'5'重复序列的两个串联拷贝。主要类型缺少映射到重复序列区域的约300个碱基对(bp);因此,它可能仅包含该序列的单个拷贝。用于确定这些结构的策略涉及在ASV DNA的物理图谱上为限制性内切酶指定20多个切割位点。比较了几种ASV菌株的这些位点,并已确定这些位点与ASV env和src基因中经常观察到的缺失有关。