Steffen D L, Taylor B A, Weinberg R A
J Virol. 1982 Apr;42(1):165-75. doi: 10.1128/JVI.42.1.165-175.1982.
The gel electrophoresis-hybridization technique of Southern was used to analyze genetically transmitted proviruses coding for the AKV strain of murine leukemia virus. We were able to identify the restriction endonuclease EcoRI fragments containing two previously unidentified, genetically transmitted AKV proviruses of AKR mice. Comparison of different sublines of AKR mice revealed considerable heterogeneity in their complement of germ line proviruses. This heterogeneity provides evidence that the provirus complement of AKR mice is not stable. Rather, the number of genetically transmitted proviruses increases during inbreeding. Examination of a series of sublines of the C3H strain indicated that this amplification is dependent on viremia. We estimate that, in viremic strains of mice, one new provirus becomes fixed in the germ line every 15 to 30 years.
采用Southern的凝胶电泳-杂交技术分析编码小鼠白血病病毒AKV株的遗传传递前病毒。我们能够鉴定出含有两种先前未鉴定的、AKR小鼠遗传传递的AKV前病毒的限制性内切酶EcoRI片段。对不同AKR小鼠亚系的比较显示,它们种系前病毒的组成存在相当大的异质性。这种异质性证明AKR小鼠的前病毒组成不稳定。相反,在近亲繁殖过程中,遗传传递的前病毒数量会增加。对C3H品系一系列亚系的检测表明,这种扩增依赖于病毒血症。我们估计,在有病毒血症的小鼠品系中,每15到30年就有一个新的前病毒固定在种系中。