Canaani E, Aaronson S A
Proc Natl Acad Sci U S A. 1979 Apr;76(4):1677-81. doi: 10.1073/pnas.76.4.1677.
The topography of endogenous type C viral sequences in mouse cellular DNA was investigated by EcoRI nuclease restriction and application of the Southern blotting technique. The DNAs from one outbred and five inbred strains were resolved into 20-35 fragments containing viral sequences, distributed in unique, though related, patterns for each mouse strain. Different normal tissues from the same animal were indistinguishable in their DNA patterns, suggesting that tissue differentiation is not associated with gross alteration in the topography of endogenous type C virus sequences. Tumor tissues from spontaneous lymphomas of AKR/J mice were similarly analyzed. In four out of seven individual tumors we detected the emergence of one or two new virus-containing DNA fragments. The mass of these fragment varied, indicating different insertion sites of the new viral sequences. The detection of these new viral sequences suggests that each tumor was composed of descendents of only one or a few cells.
通过EcoRI核酸酶限制和Southern印迹技术的应用,研究了小鼠细胞DNA中内源性C型病毒序列的拓扑结构。来自一个远交系和五个近交系的DNA被分解为20 - 35个含有病毒序列的片段,每个小鼠品系以独特但相关的模式分布。同一动物的不同正常组织在其DNA模式上无法区分,这表明组织分化与内源性C型病毒序列拓扑结构的总体改变无关。对AKR/J小鼠自发淋巴瘤的肿瘤组织进行了类似分析。在七个个体肿瘤中的四个中,我们检测到一两个新的含病毒DNA片段的出现。这些片段的大小各不相同,表明新病毒序列的插入位点不同。这些新病毒序列的检测表明,每个肿瘤仅由一个或几个细胞的后代组成。