Leiden J M, Frenkel N, Rapp F
J Virol. 1980 Jan;33(1):272-85. doi: 10.1128/JVI.33.1.272-285.1980.
We have used a novel filter hybridization approach to detect and map the herpes simplex virus (HSV) DNA sequences which are present in four HSV thymidine kinase (HSVtk+)-transformed cell lines which were derived by exposure of thymidine kinase negative (tk-) mouse cells to UV light-irradiated HSV type 2 (HSV-2). In addition, we have mapped the HSV-1 DNA sequences which are present in two HSV-1tk+-transformed cell lines produced by transfection of tk- mouse cells with sheared HSV-1 DNA. The results of these studies can be summarized as follows. (i) The only HSV DNA sequences which were common to all HSVtk+-transformed cells were those located between map coordinates 0.28 and 0.32. Thus, this region contains all of the viral DNA sequences which are necessary for the expression of HSV-mediated tk transformation. (ii) Many of the cell lines also contained variable amounts of non-tk gene viral DNA sequences located between map coordinates 0.11 to 0.57 and 0.82 to 1.00, suggesting that incorporation of the viral DNA sequences located between these map coordinates is a relatively random event. (iii) The viral DNA sequences located between map coordinates 0 to 0.11 and 0.57 to 0.82 were uniformly absent from all of the HSVtk+ cell lines tested, suggesting that there is a strong negative selective pressure against incorporation of these viral DNA sequences.
我们采用了一种新型的滤膜杂交方法,来检测和定位单纯疱疹病毒(HSV)的DNA序列,这些序列存在于四个HSV胸苷激酶(HSVtk +)转化的细胞系中,这些细胞系是通过将胸苷激酶阴性(tk -)小鼠细胞暴露于紫外线照射的2型单纯疱疹病毒(HSV - 2)而获得的。此外,我们还定位了存在于两个HSV - 1tk +转化细胞系中的HSV - 1 DNA序列,这两个细胞系是通过用剪切的HSV - 1 DNA转染tk -小鼠细胞产生的。这些研究结果可总结如下:(i)所有HSVtk +转化细胞共有的唯一HSV DNA序列位于图谱坐标0.28至0.32之间。因此,该区域包含了HSV介导的tk转化表达所必需的所有病毒DNA序列。(ii)许多细胞系还含有位于图谱坐标0.11至0.57和0.82至1.00之间的可变数量的非tk基因病毒DNA序列,这表明这些图谱坐标之间的病毒DNA序列的整合是一个相对随机的事件。(iii)在所有测试的HSVtk +细胞系中,图谱坐标0至0.11和0.57至0.82之间的病毒DNA序列均不存在,这表明对这些病毒DNA序列的整合存在强烈的负选择压力。