Sekiguchi M, Nakabeppu Y, Sakumi K, Tuzuki T
Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
J Cancer Res Clin Oncol. 1996;122(4):199-206. doi: 10.1007/BF01209646.
Alkylation of DNA at the 0(6) position of guanine is regarded as one o f the most critical events leading to induction of mutations and cancers in organisms. Once 0(6)-methylguanine is formed, it can pair with thymine during DNA replication, the result being a conversion of the guanine.cytosine to an adenine.thymine pair in DNA, and such mutations are often found in tumors induced by alkylating agents. To counteract such effects, organisms possess a mechanism to repair 0(6)-methylguanine in DNA. An enzyme, 0(6)-methylguanine-DNA methyltransferase, is present in various organism, from bacteria to human cells, and appears to be responsible for preventing the occurrence of such mutations. The enzyme transfers methyl groups from 0(6)-methylguanine and other methylated moieties of the DNA to its own molecule, thereby repairing DNA lesions in a single-step reaction. To elucidate the role of methyltransferase in preventing cancers, animal models with altered levels of enzyme activity were generated. Transgenic mice carrying the foreign methyltransferase gene with functional promoters had higher levels of methyltransferase activity and showed a decreased susceptibility to N-nitroso compounds in regard to liver carcinogenesis. Mouse lines deficient in the methyltransferase gene, which were established by gene targeting, exhibited an extraordinarily high sensitivity to an alkylating carcinogen.
鸟嘌呤0(6)位的DNA烷基化被认为是导致生物体中突变和癌症发生的最关键事件之一。一旦形成0(6)-甲基鸟嘌呤,它在DNA复制过程中可与胸腺嘧啶配对,结果是DNA中的鸟嘌呤-胞嘧啶对转变为腺嘌呤-胸腺嘧啶对,并且这种突变常出现在由烷基化剂诱导的肿瘤中。为抵消这种影响,生物体拥有一种修复DNA中0(6)-甲基鸟嘌呤的机制。一种名为0(6)-甲基鸟嘌呤-DNA甲基转移酶的酶存在于从细菌到人类细胞的各种生物体中,似乎负责防止此类突变的发生。该酶将甲基从0(6)-甲基鸟嘌呤和DNA的其他甲基化部分转移到其自身分子上,从而在一步反应中修复DNA损伤。为阐明甲基转移酶在预防癌症中的作用,构建了酶活性水平改变的动物模型。携带具有功能性启动子的外源甲基转移酶基因的转基因小鼠具有较高的甲基转移酶活性水平,并且在肝癌发生方面对N-亚硝基化合物的易感性降低。通过基因靶向建立的甲基转移酶基因缺陷小鼠品系对烷基化致癌物表现出极高的敏感性。