Costa de Oliveira R, Laval J, Boiteux S
Mutat Res. 1987 Jan;183(1):11-20. doi: 10.1016/0167-8817(87)90040-x.
The induction of SOS and adaptive responses by alkylating agents was studied in Escherichia coli mutants tagA and alkA deficient in 3-methyladenine-DNA glycosylase activities. The SOS response was measured using an sfiA::lacZ operon fusion. The sfiA operon, in the double mutant tagA alkA, is induced at 5-50-fold lower concentrations of all tested methylating and ethylating compounds, as compared to the wild-type strain. In all cases, the tagA mutation, which inactivates the constitutive and specific 3-alkyladenine-DNA glycosylase I (TagI), sensitizes the strain to the SOS response. The sensitization effect of alkA mutation, which inactivates the inducible 3-alkyladenine-DNA glycosylase II (TagII), is observed under conditions which allow the induction of the adaptive response. We conclude that the persistence of 3-methyladenine and 3-ethyladenine residues in DNA most likely leads to the induction of the SOS functions. In contrast, the adaptive response, evaluated by O6-methylguanine-DNA methyltransferase activity in cell extracts, was not affected by either tagA or alkA mutations. The results suggest that the SOS and adaptive responses use different alkylation products as an inducing "signal". However, adaptation protein TagII inhibits the induction of the SOS response to some extent, due to its action at the level of signal production. Finally, we provide conditions to improve short-term bacterial tests for the detection of genotoxic alkylating agents.
在缺乏3-甲基腺嘌呤-DNA糖基化酶活性的大肠杆菌突变体tagA和alkA中,研究了烷基化剂对SOS和适应性反应的诱导作用。使用sfiA::lacZ操纵子融合来测量SOS反应。与野生型菌株相比,在双突变体tagA alkA中,sfiA操纵子在所有测试的甲基化和乙基化化合物浓度低5至50倍时被诱导。在所有情况下,使组成型和特异性3-烷基腺嘌呤-DNA糖基化酶I(TagI)失活的tagA突变使菌株对SOS反应敏感。使诱导型3-烷基腺嘌呤-DNA糖基化酶II(TagII)失活的alkA突变的敏感化作用,在允许诱导适应性反应的条件下观察到。我们得出结论,DNA中3-甲基腺嘌呤和3-乙基腺嘌呤残基的持续存在很可能导致SOS功能的诱导。相反,通过细胞提取物中的O6-甲基鸟嘌呤-DNA甲基转移酶活性评估的适应性反应不受tagA或alkA突变的影响。结果表明,SOS和适应性反应使用不同的烷基化产物作为诱导“信号”。然而,由于其在信号产生水平的作用,适应性蛋白TagII在一定程度上抑制SOS反应的诱导。最后,我们提供了改进用于检测遗传毒性烷基化剂的短期细菌试验的条件。