Curran T, Miller A D, Zokas L, Verma I M
Cell. 1984 Feb;36(2):259-68. doi: 10.1016/0092-8674(84)90219-8.
The FBJ murine osteosarcoma virus (FBJ-MuSV) induces osteosarcomas in mice and transforms fibroblasts in vitro. It contains an oncogene termed v-fos derived from a normal cellular gene by recombination with an associated helper virus. The product of the v-fos gene is a 55,000 dalton protein, p55v-fos. This protein was found in the nuclei of cells containing amplified levels of the v-fos gene, and also in the nuclei of virus-transformed cells. The c-fos protein was localized in the nuclei of normal mouse amnion cells and in the nuclei of cells transformed by a recombinant plasmid that expresses the c-fos gene product. However, p55c-fos undergoes more extensive post-translational modification in the nucleus than p55v-fos. Immunofluorescence data indicate that the level of p55c-fos in normal mouse amnion cells is similar to that found in fibroblasts transformed by the v-fos or c-fos proteins.
FBJ小鼠骨肉瘤病毒(FBJ-MuSV)可在小鼠体内诱发骨肉瘤,并在体外转化成纤维细胞。它含有一个通过与相关辅助病毒重组而从正常细胞基因衍生而来的癌基因,称为v-fos。v-fos基因的产物是一种55,000道尔顿的蛋白质,即p55v-fos。在含有扩增水平v-fos基因的细胞的细胞核中以及病毒转化细胞的细胞核中都发现了这种蛋白质。c-fos蛋白定位于正常小鼠羊膜细胞的细胞核以及由表达c-fos基因产物的重组质粒转化的细胞的细胞核中。然而,与p55v-fos相比,p55c-fos在细胞核中经历了更广泛的翻译后修饰。免疫荧光数据表明,正常小鼠羊膜细胞中p55c-fos的水平与v-fos或c-fos蛋白转化的成纤维细胞中的水平相似。