Boiteux S, Laval J
Biochimie. 1982 Aug-Sep;64(8-9):637-41. doi: 10.1016/s0300-9084(82)80103-x.
After treatment of poly(dC) by the simple alkylating agent (3H)dimethylsulfate, 90 per cent of the radioactivity cochromatographied with 3-methylcytosine and 10 per cent with 5-methylcytosine which is the normally occurring methylated base. In order to study the influence of 3-methylcytosine on DNA replication, untreated and DMS-treated poly(dC) were used as templates for E. coli DNA polymerase I. The alkylation of poly(dC) inhibits DNA chain elongation, and does not induce any mispairing under high fidelity conditions. The alteration of DNA polymerase I fidelity by manganese ions allows some replication of 3-methylcytosine which mispairs with either dAMP or dTMP. Our results suggest that 3-methylcytosine could be responsible, at least partially, for the killing and the mutagenesis observed after cell treatment by alkylating agents.
用简单的烷基化剂(³H)硫酸二甲酯处理聚(dC)后,90%的放射性与3 - 甲基胞嘧啶共层析,10%与5 - 甲基胞嘧啶共层析,5 - 甲基胞嘧啶是正常存在的甲基化碱基。为了研究3 - 甲基胞嘧啶对DNA复制的影响,未处理的和经硫酸二甲酯处理的聚(dC)被用作大肠杆菌DNA聚合酶I的模板。聚(dC)的烷基化抑制DNA链延伸,并且在高保真条件下不诱导任何错配。锰离子改变DNA聚合酶I的保真度会使3 - 甲基胞嘧啶与dAMP或dTMP发生错配从而得以进行一些复制。我们的结果表明,3 - 甲基胞嘧啶可能至少部分地导致了细胞经烷基化剂处理后出现的杀伤和诱变现象。