Türler H
J Virol. 1974 Feb;13(2):285-90. doi: 10.1128/JVI.13.2.285-290.1974.
Secondary mouse embryo (ME) cultures which had been grown prior to infection in the presence of 5-bromodeoxyuridine (BUdR) and 5-fluorodeoxy-uridine were found to be permissive for polyoma virus (16). The DNA extracted from the progeny virus yielded two bands on CsCl isopycnic centrifugation. The light band (LL) contained supercoiled circular (polyoma DNA I), open circular (polyoma DNA II), and linear (polyoma DNA III) molecules, as was seen by electron microscopy. The hybrid band (HL) contained exclusively linear molecules. This DNA was pure, density - labeled, pseudovirion DNA, i.e., fragmented HL mouse DNA. The quantitative comparison of HL and LL polyoma DNA III from six different virus preparations always revealed an excess of HL DNA, the ratio of HL/LL being between 1.2 and 2.2. These results led to the conclusion that in BUdR-prelabeled, polyoma-infected ME cells pseudovirion DNA is excised both from unreplicated and newly replicated regions of mouse DNA.
在5-溴脱氧尿苷(BUdR)和5-氟脱氧尿苷存在的情况下,于感染前培养的二代小鼠胚胎(ME)培养物被发现对多瘤病毒具有易感性(16)。从子代病毒中提取的DNA在CsCl等密度离心时产生两条带。通过电子显微镜观察,轻带(LL)包含超螺旋环状(多瘤病毒DNA I)、开环(多瘤病毒DNA II)和线性(多瘤病毒DNA III)分子。杂交带(HL)仅包含线性分子。这种DNA是纯的、密度标记的假病毒体DNA,即片段化的HL小鼠DNA。对六种不同病毒制剂的HL和LL多瘤病毒DNA III进行定量比较,总是发现HL DNA过量,HL/LL的比值在1.2至2.2之间。这些结果得出结论,在预先用BUdR标记、感染多瘤病毒的ME细胞中,假病毒体DNA从小鼠DNA的未复制区域和新复制区域均被切除。