Samson L, Derfler B, Waldstein E A
Proc Natl Acad Sci U S A. 1986 Aug;83(15):5607-10. doi: 10.1073/pnas.83.15.5607.
The ada-alkB operon protects Escherichia coli against the effects of many alkylating agents. We have subcloned it into the pSV2 mammalian expression vector to yield pSV2ada-alkB, and this plasmid has been introduced into Mer- HeLa S3 cells, which are extremely sensitive to killing and induction of sister chromatid exchange by alkylating agents. One transformant (the S3-9 cell line) has several integrated copies of pSV2ada-alkB and was found to express a very high level of the ada gene product, the 39-kDa O6-methylguanine-DNA methyltransferase. S3-9 cells were found to have become resistant to killing and induction of sister chromatid exchange by two alkylating agents, N-methyl-N'-nitro-N-nitrosoguanidine and N,N'-bis(2-chloroethyl)-N-nitro-sourea. This shows that bacterial DNA alkylation-repair genes are able to suppress the alkylation-repair defects in human Mer- cells.
ada-alkB操纵子可保护大肠杆菌免受多种烷化剂的影响。我们已将其亚克隆到pSV2哺乳动物表达载体中,得到pSV2ada-alkB,并且该质粒已被导入Mer- HeLa S3细胞中,这些细胞对烷化剂诱导的杀伤和姐妹染色单体交换极为敏感。一个转化体(S3-9细胞系)含有多个整合的pSV2ada-alkB拷贝,并且发现其表达非常高水平的ada基因产物,即39 kDa的O6-甲基鸟嘌呤-DNA甲基转移酶。结果发现,S3-9细胞对两种烷化剂N-甲基-N'-硝基-N-亚硝基胍和N,N'-双(2-氯乙基)-N-硝基脲的杀伤和姐妹染色单体交换诱导产生了抗性。这表明细菌DNA烷基化修复基因能够抑制人类Mer-细胞中的烷基化修复缺陷。