Graham F L, Smiley J, Russell W C, Nairn R
J Gen Virol. 1977 Jul;36(1):59-74. doi: 10.1099/0022-1317-36-1-59.
Human embryonic kidney cells have been transformed by exposing cells to sheared fragments of adenovirus type 5 DNA. The transformed cells (designated 293 cells) exhibited many of the characteristics of transformation including the elaboration of a virus-specific tumour antigen. Analysis of the polypeptides synthesized in the 293 cells by labelling with 35S-methionine and SDS PAGE showed a variable pattern of synthesis, different in a number of respects from that seen in otheruman cells. On labelling the surface of cells by lactoperoxidase catalysed radio-iodination, the absence of a labelled polypeptide analogous to the 250 K (LETS) glycoprotein was noted. Hybridization of labelled cellular RNA with restriction fragments of adenovirus type 5 DNA indicated transcription of a portion of the adenovirus genome at the conventional left hand end.
通过将人胚肾细胞暴露于5型腺病毒DNA的剪切片段,这些细胞发生了转化。转化后的细胞(命名为293细胞)展现出许多转化特征,包括产生一种病毒特异性肿瘤抗原。用35S-甲硫氨酸标记并通过SDS-PAGE分析293细胞中合成的多肽,结果显示出可变的合成模式,在许多方面与其他人类细胞中所见的不同。在用乳过氧化物酶催化的放射性碘化标记细胞表面时,发现不存在类似于250K(LETS)糖蛋白的标记多肽。用标记的细胞RNA与5型腺病毒DNA的限制性片段杂交,表明在传统的左手端转录了腺病毒基因组的一部分。