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Mutation spectra of the drinking water mutagen 3‐chloro‐4‐methyl‐5‐hydroxy‐2(5 H )‐furanone (MCF) in Salmonella TA100 and TA104: Comparison to MX
Author(s) -
Shaughnessy Daniel T.,
Ohe Takeshi,
Landi Stefano,
Warren Sarah H.,
Richard Ann M.,
Munter Tony,
Franzén Robert,
Kronberg Leif,
DeMarini David M.
Publication year - 2000
Publication title -
environmental and molecular mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 87
eISSN - 1098-2280
pISSN - 0893-6692
DOI - 10.1002/(sici)1098-2280(2000)35:2<106::aid-em5>3.0.co;2-u
Subject(s) - mutagen , mutagenesis , chemistry , adduct , mutation , salmonella , dna , stereochemistry , microbiology and biotechnology , biochemistry , genetics , biology , gene , bacteria , organic chemistry
Abstract The chlorinated drinking water mutagen 3‐chloro‐4‐methyl‐5‐hydroxy‐2(5H)‐furanone (MCF) occurs at concentrations similar to or greater than that of the related furanone 3‐chloro‐4‐(dichloromethyl)‐5‐hydroxy‐2(5 H )‐furanone (MX). MCF and MX differ structurally only by replacement of a 3‐methyl in MCF with a 3‐dichloromethyl in MX; yet, MCF is significantly less mutagenic than MX and produces different adducts when reacted with nucleosides or DNA. To explore further the effects that these structural differences might have on the biological activity of MCF and MX, we determined the mutation spectra of MCF in Salmonella strains TA100 and TA104 and of MX in strain TA104; the spectrum of MX in TA100 had been determined previously. In TA100, which presents only GC targets for mutagenesis, MCF induced primarily (75%) GC → TA transversions, with most of the remaining revertants (20%) being GC → AT transitions. This spectrum was not significantly different from that of MX in TA100 ( P = 0.07). In TA104, which presents both GC and AT targets, MCF induced a lower percentage (57%) of GC → TA transversions, with most of the remaining revertants (33%) being AT → TA transversions. In contrast, MX induced almost only (98%) GC → TA transversions in TA104, with the remaining revertants (2%) being AT → TA transversions. Thus, almost all (98%) of the MX mutations were targeted at GC sites in TA104, whereas only 63% of the MCF mutations were so targeted. These results are consistent with the published findings that MX: (1) forms an adduct on guanosine when reacted with guanosine, (2) induces apurinic sites in DNA, and (3) forms a minor adduct on adenosine when reacted with adenosine or DNA. The results are also consistent with evidence that MCF forms adenosine adducts when reacted with adenosine. Our results show that the replacement of the 4‐methyl in MCF with a 4‐dichloromethyl to form MX not only increases dramatically the mutagenic potency but also shifts significantly the mutagenic specificity from almost equal targeting of GC and AT sites by MCF to almost exclusive targeting of GC sites by MX. Environ. Mol. Mutagen. 35:106–113, 2000 Published 2000 Wiley‐Liss, Inc.