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Mutations induced by glyoxal and methylglyoxal in mammalian cells
Author(s) -
Hiroyuki Kamiya,
Hidesuke Kaji,
Hiroshi Kasai
Publication year - 2000
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/44.1.3
Subject(s) - methylglyoxal , glyoxal , mutant , mutation , microbiology and biotechnology , shuttle vector , chemistry , base pair , mutagenesis , lactoylglutathione lyase , plasmid , genetics , biology , biochemistry , gene , recombinant dna , vector (molecular biology) , enzyme , organic chemistry
To investigate the mutation spectra of glyoxal and methylglyoxal in mammalian cells, we analyzed mutations in a bacterial suppressor tRNA (supF) gene in the shuttle vector plasmid pMY189. The cytotoxicity and the mutation frequency increased according to the doses of glyoxal and methylglyoxal. The majority of glyoxal-induced mutations (65%) were base-pair substitutions, in which G:C-->C:G transversions were predominant. In the mutants induced by methylglyoxal, multi-base deletions were predominant (50%), followed by base-pair substitutions (35%), in which G:C-->C:G and G:C-->T:A transversions were predominant.

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