Tainsky M A, Cooper C S, Giovanella B C, Vande Woude G F
Science. 1984 Aug 10;225(4662):643-5. doi: 10.1126/science.6740333.
Early passages of the human teratocarcinoma cell line PA1 are not tumorigenic in nude mice, while late passages are. A transforming gene present in late passages of PA1 cells was isolated as a biologically active molecular clone and is a new isolate of the human rasN locus. Its transforming activity is due to a single G---A (G, guanine; A, adenine) point mutation at the codon for amino acid 12 which changes the codon for glycine so that an aspartic acid residue is expressed. In contrast to late passage PA1 cells (passages 106, 330, and 338), DNA from the PA1 cell line at early passages (passage 36) does not yield rasN foci in DNA transfection assays. Thus, the presence of an activated rasN in PA1 cells correlates with enhanced tumorigenicity of the cell line and, more importantly, may have arisen during cell culture in vitro.
人畸胎瘤细胞系PA1的早期传代细胞在裸鼠中不具有致瘤性,而晚期传代细胞则具有致瘤性。从PA1细胞的晚期传代细胞中分离出一个具有生物活性的分子克隆,它是人类rasN基因座的一个新分离物,该转化基因导致了这种变化。其转化活性是由于第12位氨基酸密码子处的单个G→A(G,鸟嘌呤;A,腺嘌呤)点突变,该突变改变了甘氨酸的密码子,从而表达出一个天冬氨酸残基。与晚期传代的PA1细胞(传代106、330和338)相比,早期传代(传代36)的PA1细胞系DNA在DNA转染试验中不会产生rasN灶。因此,PA1细胞中活化的rasN的存在与该细胞系增强的致瘤性相关,更重要的是,它可能是在体外细胞培养过程中产生的。