TY - JOUR
T1 - Mutagenic activity and specificity of N-nitrosomethylaniline and N-nitrosodiphenylamine in Salmonella
AU - Zielenska, M.
AU - Guttenplan, J. B.
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1988/11
Y1 - 1988/11
N2 - 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 consitent with the hypothesis that NMA and NDphA lead to DNA damage of different nature than that produced by other nitrosamines.
AB - 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 consitent with the hypothesis that NMA and NDphA lead to DNA damage of different nature than that produced by other nitrosamines.
KW - N-Nitrosodiphenylamine
KW - N-Nitrosomethylaniline
KW - Salmonella/microsome assay
KW - UvrB mutation
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U2 - 10.1016/0027-5107(88)90189-3
DO - 10.1016/0027-5107(88)90189-3
M3 - Article
C2 - 3054528
AN - SCOPUS:0023682767
SN - 0027-5107
VL - 202
SP - 269
EP - 276
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 1
ER -