Mackay W J, Han S, Samson L D
Department of Molecular and Cellular Toxicology, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
J Bacteriol. 1994 Jun;176(11):3224-30. doi: 10.1128/jb.176.11.3224-3230.1994.
The Escherichia coli Ada and Ogt DNA methyltransferases (MTases) are known to transfer simple alkyl groups from O6-alkylguanine and O4-alkylthymine, directly restoring these alkylated DNA lesions to guanine and thymine. In addition to being exquisitely sensitive to the mutagenic effects of methylating agents, E. coli ada ogt null mutants display a higher spontaneous mutation rate than the wild type. Here, we determined which base substitution mutations are elevated in the MTase-deficient cells by monitoring the reversion of six mutated lacZ alleles that revert via each of the six possible base substitution mutations. During exponential growth, the spontaneous rate of G:C to A:T transitions and G:C to C:G transversions was elevated about fourfold in ada ogt double mutant versus wild-type E. coli. Furthermore, compared with the wild type, stationary populations of the MTase-deficient E. coli (under lactose selection) displayed increased G:C to A:T and A:T to G:C transitions (10- and 3-fold, respectively) and increased G:C to C:G, A:T to C:G, and A:T to T:A transversions (10-, 2.5-, and 1.7-fold, respectively). ada and ogt single mutants did not suffer elevated spontaneous mutation rates for any base substitution event, and the cloned ada and ogt genes each restored wild-type spontaneous mutation rates to the ada ogt MTase-deficient strains. We infer that both the Ada MTase and the Ogt MTase can repair the endogenously produced DNA lesions responsible for each of the five base substitution events that are elevated in MTase-deficient cells. Simple methylating and ethylating agents induced G:C to A:T and A:T to G:C transitions in these strains but did not significantly induce G:C to C:G, A:T to C:G, and A:T to T:A transversions. We deduce that S-adenosylmethionine (known to e a weak methylating agent) is not the only metabolite responsible for endogenous DNA alkylation and that at least some of the endogenous metabolites that cause O-alkyl DNA damage in E. coli are not simple methylating or ethylating agents.
已知大肠杆菌的Ada和Ogt DNA甲基转移酶(MTases)能从O6 - 烷基鸟嘌呤和O4 - 烷基胸腺嘧啶转移简单的烷基基团,直接将这些烷基化的DNA损伤恢复为鸟嘌呤和胸腺嘧啶。除了对甲基化剂的诱变作用极为敏感外,大肠杆菌ada ogt基因缺失突变体的自发突变率也高于野生型。在此,我们通过监测六个经六种可能的碱基替换突变回复的lacZ突变等位基因的回复情况,确定了在MTase缺陷细胞中哪些碱基替换突变有所增加。在指数生长期,与野生型大肠杆菌相比,ada ogt双突变体中G:C到A:T的转换以及G:C到C:G的颠换的自发率提高了约四倍。此外,与野生型相比,MTase缺陷型大肠杆菌(在乳糖选择下)的静止群体中G:C到A:T和A:T到G:C的转换增加(分别为10倍和3倍),G:C到C:G、A:T到C:G以及A:T到T:A的颠换也增加(分别为10倍、2.5倍和1.7倍)。ada和ogt单突变体在任何碱基替换事件中都没有自发突变率升高的情况,并且克隆的ada和ogt基因各自将野生型自发突变率恢复到ada ogt MTase缺陷型菌株中。我们推断,Ada MTase和Ogt MTase都可以修复内源性产生的DNA损伤,这些损伤导致了MTase缺陷细胞中增加的五种碱基替换事件中的每一种。简单的甲基化和乙基化剂在这些菌株中诱导了G:C到A:T和A:T到G:C的转换,但没有显著诱导G:C到C:G、A:T到C:G以及A:T到T:A的颠换。我们推断,S - 腺苷甲硫氨酸(已知是一种弱甲基化剂)不是内源性DNA烷基化的唯一代谢产物,并且在大肠杆菌中导致O - 烷基DNA损伤的至少一些内源性代谢产物不是简单的甲基化或乙基化剂。