Burns P A, Gordon A J, Glickman B W
J Mol Biol. 1987 Apr 5;194(3):385-90. doi: 10.1016/0022-2836(87)90668-1.
N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced forward mutations within the first 540 base-pairs of the lacI gene of Escherichia coli were cloned and sequenced. In total, 167 MNNG-induced independent mutations were characterized, with G.C to A.T transitions accounting for all but three of the mutations. This mutagenic specificity is consistent with the mispairing predicted by the methylation of the O6 position of guanine. The characterization of such large numbers of mutations permitted an analysis of the influence of local DNA sequence on mutagenesis. This analysis revealed a strong influence by the 5' flanking base. On average, guanine residues preceded (5') by a guanine or an adenine residue were, respectively, nine times and five times more likely to mutate after treatment with MNNG than those preceded by a pyrimidine residue.
对N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的大肠杆菌lacI基因前540个碱基对内的正向突变进行了克隆和测序。总共鉴定了167个MNNG诱导的独立突变,除三个突变外,其余所有突变均为G.C到A.T的转换。这种诱变特异性与鸟嘌呤O6位甲基化预测的错配一致。如此大量突变的表征使得能够分析局部DNA序列对诱变的影响。该分析揭示了5'侧翼碱基的强烈影响。平均而言,在用MNNG处理后,鸟嘌呤残基5'端分别为鸟嘌呤或腺嘌呤残基的情况下,其突变的可能性分别比嘧啶残基5'端的鸟嘌呤残基高九倍和五倍。