Ullman B, Levinson B B, Ullman D H, Martin D W
J Biol Chem. 1979 Sep 25;254(18):8736-9.
Two clones were isolated from mutagenized mouse T-lymphoma cells (S49) which are over 90% deficient in uridine-cytidine kinase. The first clone, AU-200-1, was isolated in two steps by virtue of its resistance to 6-azauridine; whereas the second clone, FU3-70G, was isolated in three steps after exposure to three increasing concentrations of 5-fluorouracil. Extracts of both the AU-200-1 and the FU3-70G cell lines lacked over 90% of the capacity of those from wild type cells to phosphorylate either uridine or cytidine. Furthermore, the uptake of radioactive uridine and cytidine from the medium by intact AU-200-1 and FU3-70G cells was less than 5% of that found for intact wild type cells. By growth rate experiments, these uridine-cytidine kinase-deficient cell lines have altered sensitivities to the toxic pyrimidine analogs, 6-azauridine, 5-fluorouracil, and 5-fluorouridine and thus have been useful in elucidating the biochemical determinants involved in the metabolism of these compounds.
从诱变的小鼠T淋巴瘤细胞(S49)中分离出两个克隆,这些细胞的尿苷 - 胞苷激酶缺陷超过90%。第一个克隆AU - 200 - 1通过其对6 - 氮杂尿苷的抗性分两步分离得到;而第二个克隆FU3 - 70G在暴露于三种浓度递增的5 - 氟尿嘧啶后分三步分离得到。AU - 200 - 1和FU3 - 70G细胞系的提取物磷酸化尿苷或胞苷的能力比野生型细胞提取物低90%以上。此外,完整的AU - 200 - 1和FU3 - 70G细胞从培养基中摄取放射性尿苷和胞苷的量不到完整野生型细胞的5%。通过生长速率实验,这些尿苷 - 胞苷激酶缺陷的细胞系对毒性嘧啶类似物6 - 氮杂尿苷、5 - 氟尿嘧啶和5 - 氟尿苷的敏感性发生了改变,因此在阐明这些化合物代谢过程中的生化决定因素方面很有用。