Goff S P, Gilboa E, Witte O N, Baltimore D
Cell. 1980 Dec;22(3):777-85. doi: 10.1016/0092-8674(80)90554-1.
Circular double-stranded DNA produced after infection of mouse cells with Abelson murine leukemia virus (A-MuLV) was isolated and cloned in the phage vector Charon 21A. The resulting clones of the A-MuLV genome show homology to the ends of Moloney MuLV and to a 3.5 kb central region containing sequences unique to Abelson virus. A 2.3 kb restriction fragment containing only A-MuLV-specific sequences was subcloned in the plasmid vector pBR322 and used as a probe for the cellular gene that had been acquired by the virus. DNA from all inbred mouse lines examined contains an identical region of homology spread out over 11 to 20 kb. The cellular gene contains intervening sequences which are lacking in the viral genome. Rat, Chinese hamster, rabbit, chicken and human DNA also show homology to the viral probe.
用阿贝尔逊鼠白血病病毒(A-MuLV)感染小鼠细胞后产生的环状双链DNA被分离出来,并克隆到噬菌体载体Charon 21A中。所得的A-MuLV基因组克隆显示与莫洛尼鼠白血病病毒的末端以及与一个包含阿贝尔逊病毒特有序列的3.5 kb中央区域具有同源性。一个仅包含A-MuLV特异性序列的2.3 kb限制性片段被亚克隆到质粒载体pBR322中,并用作病毒所获得的细胞基因的探针。所检测的所有近交系小鼠的DNA都含有一个相同的同源区域,该区域分布在11至20 kb范围内。细胞基因含有病毒基因组中所没有的间隔序列。大鼠、中国仓鼠、兔子、鸡和人类的DNA也显示与病毒探针具有同源性。