Sen A, Todaro G J
Proc Natl Acad Sci U S A. 1978 Apr;75(4):1647-51. doi: 10.1073/pnas.75.4.1647.
Mouse cells transformed by DNA and RNA tumor viruses and by chemical carcinogens have been examined for the presence of specific DNA-binding proteins by DNA-cellulose chromatography. Using mouse DNA-cellulose we have obtained single-stranded DNA-binding proteins from two clones transformed by chemical carcinogens. Simian virus 40 transformants also have a DNA-binding protein [the tumor (T) antigen] that binds to mouse and human DNA with comparable affinity. Mouse sarcoma virus-transformed cells and two other chemically transformed clones showed no difference in DNA-binding protein pattern compared to the untransformed parental cell. The DNA-binding proteins isolated from the chemically transformed cell clones are between 25,000 and 30,000 daltons by sodium dodecyl sulfate/polyacrylamide gel electrophoresis. These cellular "T proteins" bind to the homologous mouse cellular DNA with a higher affinity than to heterologous human cellular DNA.
通过DNA - 纤维素色谱法检测了经DNA和RNA肿瘤病毒以及化学致癌物转化的小鼠细胞中特定DNA结合蛋白的存在情况。使用小鼠DNA - 纤维素,我们从两个经化学致癌物转化的克隆中获得了单链DNA结合蛋白。猿猴病毒40转化体也有一种DNA结合蛋白[肿瘤(T)抗原],它以相当的亲和力与小鼠和人类DNA结合。与未转化的亲本细胞相比,小鼠肉瘤病毒转化细胞和其他两个化学转化克隆在DNA结合蛋白模式上没有差异。通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳,从化学转化细胞克隆中分离出的DNA结合蛋白分子量在25,000至30,000道尔顿之间。这些细胞“T蛋白”与同源小鼠细胞DNA的结合亲和力高于与异源人类细胞DNA的结合亲和力。