Devaux J, Jouanneau J, Quibriac M, Longuet M, Le Bousse-Kerdiles M C, Auger-Buendia M A, Tavitian A
J Gen Virol. 1985 Nov;66 ( Pt 11):2407-14. doi: 10.1099/0022-1317-66-11-2407.
The 78A1 isolate of Moloney murine sarcoma virus (78A1 Mo-MuSV) was cloned from a genomic library obtained from virus producer rat cells, in the lambda vector L47. Among the recombinants hybridizing with a probe specific for the v-mos sequences, we recovered a recombinant which contained leukaemia virus (MuLV) sequences and was able to transform both mouse and rat cells in transfection experiments. The cloned provirus could be rescued by both Mo-MuLV ecotropic and amphotropic viruses in mouse cells, but only with the amphotropic helper virus in rat cells. Comparative restriction mapping indicates that the 78A1 provirus is 200 bp longer than the HT1 provirus. The difference lies in the gag-pol junction region of Mo-MuSV. Other minor differences were found in the gag region, whereas the restriction patterns of the 3' parts of the proviruses were identical.
莫洛尼鼠肉瘤病毒的78A1分离株(78A1 Mo-MuSV)是从用λ载体L47构建的、来自病毒产生大鼠细胞的基因组文库中克隆得到的。在与v-mos序列特异性探针杂交的重组体中,我们获得了一个含有白血病病毒(MuLV)序列的重组体,该重组体在转染实验中能够转化小鼠和大鼠细胞。克隆的前病毒在小鼠细胞中可被亲嗜性和兼嗜性的Mo-MuLV拯救,但在大鼠细胞中仅能被兼嗜性辅助病毒拯救。限制性图谱比较表明,78A1前病毒比HT1前病毒长200 bp。差异位于Mo-MuSV的gag-pol连接区。在gag区还发现了其他一些微小差异,而前病毒3'部分的限制性图谱是相同的。