Takechi Shinji, Yamaguchi Tadatoshi, Nomura Hajime, Minematsu Toshio, Adachi Masaru, Kurata Hirofumi, Kurata Rie
Faculty of Pharmaceutical Sciences, Sojo University Kumamoto, Japan.
Biol Pharm Bull. 2006 Jan;29(1):17-20. doi: 10.1248/bpb.29.17.
Dihydropyrazine (DHP), which induces mutagenesis in E. coli, was investigated. From analyzing mutations in the chromosomal rpoB gene, the mutation spectrum in uvrB strain revealed the different behavior on exposure to two DHP derivatives 3-hydro-2,2,5,6-tetramethylpyrazine (HTMP), and 2,3-dihydro-5,6-dimethylpyrazine (DHDMP). A higher level of DHP-induced mutation was observed, with base substitutions at G : C pairs predominant. HTMP and DHDMP increased the frequency of G : C to T : A transversions. HTMP increased the frequency of G : C to A : T transitions, than did DHDMP. These findings suggest that DHPs prefer to attack the G : C pair and that different DHP derivatives may prefer distinct mutagenic base pairs; and further, that nucleotide excision repair may be involved in the repair of DHP-induced mutations.
对能在大肠杆菌中诱发突变的二氢吡嗪(DHP)进行了研究。通过分析染色体rpoB基因中的突变,uvrB菌株中的突变谱揭示了在暴露于两种DHP衍生物3-羟基-2,2,5,6-四甲基吡嗪(HTMP)和2,3-二氢-5,6-二甲基吡嗪(DHDMP)时的不同行为。观察到较高水平的DHP诱导突变,其中以G:C碱基对的碱基替换为主。HTMP和DHDMP增加了G:C到T:A颠换的频率。HTMP比DHDMP增加了G:C到A:T转换的频率。这些发现表明,二氢吡嗪倾向于攻击G:C碱基对,不同的二氢吡嗪衍生物可能倾向于不同的诱变碱基对;此外,核苷酸切除修复可能参与了二氢吡嗪诱导突变的修复。