Zielenska M, Guttenplan J B
Department of Biochemistry, New York University Dental Center, NY 10010.
Mutat Res. 1988 Nov;202(1):269-76. doi: 10.1016/0027-5107(88)90189-3.
The carcinogenic nitrosamines, N-nitrosomethylaniline (NMA) and N-nitrosodiphenylamine (NDphA), which have been previously reported negative or very weakly mutagenic in the Salmonella/microsome assay, were found to be mutagenic in the hisG428 Salmonella strain, TA104. NMA was moderately potent and NDphA was about 10% as potent. Mutagenesis by both compounds was dependent on the uvrB mutation and enhanced in strains harboring the plasmid, pKM101. The mutational specificities of NMA and NDphA for base-pair substitutions were determined by assaying their activities in several mutants which are reverted by a limited number, or a single type of base-pair substitution mutation, and additionally by subclassification of revertants. NMA induced predominantly AT----CG transversions and NDphA induced AT----TA transversions. The specificity of NMA and NDphA for mutagenesis at AT base pairs and the lack of sensitivity of the previously employed hisG46 strains for these base changes may be the reason for the previous reports on the lack of mutagenic activity of these compounds. This specificity is quite unusual for nitrosamines and is consistent with the hypothesis that NMA and NDphA lead to DNA damage of different nature than that produced by other nitrosamines.
致癌性亚硝胺,N-亚硝基甲基苯胺(NMA)和N-亚硝基二苯胺(NDphA),先前在沙门氏菌/微粒体试验中报告为阴性或致突变性非常弱,但发现在hisG428沙门氏菌菌株TA104中具有致突变性。NMA的致突变性中等强度,NDphA的致突变性约为其10%。两种化合物的诱变作用均依赖于uvrB突变,并且在携带质粒pKM101的菌株中增强。通过在几种由有限数量或单一类型的碱基对替换突变回复的突变体中测定NMA和NDphA的活性,并通过对回复子进行亚分类,确定了它们对碱基对替换的突变特异性。NMA主要诱导AT→CG颠换,NDphA诱导AT→TA颠换。NMA和NDphA对AT碱基对诱变的特异性以及先前使用的hisG46菌株对这些碱基变化缺乏敏感性,可能是先前关于这些化合物缺乏诱变活性报道的原因。这种特异性对于亚硝胺来说非常不寻常,并且与NMA和NDphA导致的DNA损伤性质不同于其他亚硝胺产生的损伤这一假设一致。