Mutational and DNA binding specificity of the carcinogen 2-amino-3, 8-dimethylimidazo[4,5-f]quinoxaline.

Détails

ID Serval
serval:BIB_5095
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Mutational and DNA binding specificity of the carcinogen 2-amino-3, 8-dimethylimidazo[4,5-f]quinoxaline.
Périodique
Journal of Biological Chemistry
Auteur(s)
Solomon M.S., Morgenthaler P.M., Turesky R.J., Essigmann J.M.
ISSN
0021-9258
Statut éditorial
Publié
Date de publication
1996
Volume
271
Numéro
31
Pages
18368-18374
Langue
anglais
Notes
Publication types: Journal Article
Résumé
The mutagenic specificity of 2-amino-3,8-dimethylimidazo[4, 5-f]quinoxaline (MeIQx), a food-borne mutagen and carcinogen, was studied. Plasmid pK19 was modified by photolysis with the 2-azido form of the carcinogen. High pressure liquid chromatography confirmed that the photoactivated azide formed primarily C8 and N2 guanyl adducts. Transformation of modified pK19 into excision repair competent Escherichia coli resulted in dose-dependent increases in genotoxicity and in mutagenesis within the lacZalpha target sequence. Upon induction of the SOS response, a 20-fold increase in mutation frequency over background was observed. A mutational spectrum for MeIQx, generated by sequencing 125 independent mutants, revealed base substitutions (41%), frameshifts (54%), and complex mutations (5.6%); >90% of the mutations occurred at G-C base pairs. Two hotspots were evident at runs of three or five G-C base pairs; approximately 60% of the mutations occurred at the hotspot sites. The hotspot at position 2532 produced mainly base substitutions, while that at position 2576 gave exclusively frameshift mutations. A polymerase inhibition assay mapped the sites of MeIQx adducts. Arrest sites were primarily at or one base 3' to a guanine residue, which correlated well with the distribution of mutations. No direct correlation was seen, however, between intensity of modification and hotspots for mutation.
Mots-clé
Base Sequence, Binding Sites/genetics, Carcinogens/chemistry, Carcinogens/metabolism, DNA Adducts/drug effects, DNA Adducts/genetics, DNA, Bacterial/drug effects, DNA, Bacterial/genetics, DNA-Directed DNA Polymerase/metabolism, Escherichia coli/drug effects, Escherichia coli/genetics, Lac Operon, Molecular Sequence Data, Molecular Structure, Mutagens/chemistry, Mutagens/metabolism, Mutation, Quinoxalines/chemistry, Quinoxalines/metabolism, R Factors/genetics
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/11/2007 13:41
Dernière modification de la notice
08/05/2019 18:31
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