Shih C, Weinberg R A
Cell. 1982 May;29(1):161-9. doi: 10.1016/0092-8674(82)90100-3.
We have isolated the component of human bladder carcinoma cell DNA that is able to transform mouse fibroblasts. The oncogenic sequence was isolated initially from a lambda phage genomic library made from DNA of a transfected mouse cell carrying the human oncogene. A subcloned insert of 6.6 kb that carried transforming activity was amplified in the plasmid vector pBR322. The subcloned oncogene has been used as a sequence probe in Southern blot analyses. The oncogene appears to derive from sequences present in normal cellular DNA. Structural analysis has failed so far to reveal differences between the oncogene and its normal cellular homolog. The oncogene is unrelated to transforming sequences detected in a variety of other types of human tumor cell lines derived from colonic and lung carcinoma and from neuroblastoma. In contrast, the EJ bladder oncogene appears closely related to one that is active in the human T24 bladder carcinoma cell line. The oncogene appears to have undergone little, if any, amplification in several bladder carcinoma cell lines.
我们已经分离出了人膀胱癌细胞DNA中能够转化小鼠成纤维细胞的成分。致癌序列最初是从一个λ噬菌体基因组文库中分离出来的,该文库由携带人类致癌基因的转染小鼠细胞的DNA构建而成。一个携带转化活性的6.6kb亚克隆插入片段在质粒载体pBR322中得到扩增。该亚克隆致癌基因已被用作Southern印迹分析中的序列探针。该致癌基因似乎源自正常细胞DNA中存在的序列。到目前为止,结构分析未能揭示该致癌基因与其正常细胞同源物之间的差异。该致癌基因与在源自结肠癌、肺癌和神经母细胞瘤的多种其他类型人类肿瘤细胞系中检测到的转化序列无关。相比之下,EJ膀胱致癌基因似乎与在人T24膀胱癌细胞系中活跃的一个致癌基因密切相关。在几个膀胱癌细胞系中,该致癌基因似乎几乎没有(如果有的话)扩增。