Miller A D, Verma I M, Curran T
J Virol. 1985 Sep;55(3):521-6. doi: 10.1128/JVI.55.3.521-526.1985.
Both FBJ murine osteosarcoma virus (FBJ-MSV) and FBR-MSV induce transformation in tissue culture and osteogenic sarcomas in mice. In tissue culture, however, FBR-MSV induces larger foci with a shorter latency than those induced by FBJ-MSV. Transformation is dependent on expression of the fos oncogene in FBJ-MSV and of a gag-fos fusion protein in FBR-MSV. We have determined that the gag sequences can be deleted from FBR-MSV without affecting the high transforming activity of this virus in comparison to FBJ-MSV. The resultant virus, designated FBJ/R-MSV, has a protein coding region that is half the size of that of FBR-MSV and about one-third smaller than that of FBJ-MSV. Thus, FBJ/R-MSV will provide a useful tool for studying the transforming activity of the fos oncogene.
FBJ小鼠骨肉瘤病毒(FBJ-MSV)和FBR-MSV均可在组织培养中诱导细胞转化,并在小鼠中诱发骨肉瘤。然而,在组织培养中,FBR-MSV诱导的病灶比FBJ-MSV诱导的病灶更大,潜伏期更短。转化依赖于FBJ-MSV中fos癌基因的表达以及FBR-MSV中gag-fos融合蛋白的表达。我们已经确定,可以从FBR-MSV中删除gag序列,而与FBJ-MSV相比,这并不影响该病毒的高转化活性。所得病毒命名为FBJ/R-MSV,其蛋白质编码区大小是FBR-MSV的一半,比FBJ-MSV小约三分之一。因此,FBJ/R-MSV将为研究fos癌基因的转化活性提供一个有用的工具。