Steffen D, Weinberg R A
Cell. 1978 Nov;15(3):1003-10. doi: 10.1016/0092-8674(78)90284-2.
The Southern gel filter transfer technique has been used to characterize the integrated genome of Moloney murine leukemia virus (M-MuLV) and the genomes of the endogenous viruses of the mouse. Study of 10 clones of rat cell independently infected by M-MuLV indicates a minimum of 15 integration sites into which the M-MuLV provirus can be inserted. No common integration site is observed among these clones. Clones productively infected by M-MuLV acquire multiple proviruses, whereas infected cells unable to produce virus contain only one M-MuLV provirus. Once established, the integrated genomes are stable for at least two years after initial infection. The use of M-MuLV probe allows detection of a spectrum of Eco RI-cleaved mouse DNA fragments containing endogenous MuLV genomes. DNAs of different inbred laboratory mouse strains yield similar patterns of provirus with each strain showing minor characteristic differences. In some instances, mouse cells infected by M-MuLV reveal additional proviruses beyond those seen in the uninfected cell. DNAs from three different M-MuLV-induced thymomas indicate, as in rat cells, multiple possible integration sites.
采用Southern凝胶过滤转移技术对莫洛尼鼠白血病病毒(M-MuLV)的整合基因组以及小鼠内源性病毒的基因组进行了表征。对10个独立感染M-MuLV的大鼠细胞克隆的研究表明,M-MuLV前病毒可插入的整合位点至少有15个。在这些克隆中未观察到共同的整合位点。被M-MuLV有效感染的克隆会获得多个前病毒,而无法产生病毒的感染细胞仅含有一个M-MuLV前病毒。一旦建立,整合基因组在初次感染后至少两年内是稳定的。使用M-MuLV探针可检测到一系列含有内源性MuLV基因组的Eco RI酶切小鼠DNA片段。不同近交系实验小鼠品系的DNA产生相似的前病毒模式,每个品系都有微小的特征差异。在某些情况下,被M-MuLV感染的小鼠细胞显示出比未感染细胞中更多的前病毒。来自三种不同的M-MuLV诱导的胸腺瘤的DNA表明,与大鼠细胞一样,存在多个可能的整合位点。