Takahashi K, Sekiguchi M, Kawazoe Y
Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.
Biochem Biophys Res Commun. 1989 Aug 15;162(3):1376-81. doi: 10.1016/0006-291x(89)90826-7.
The present study revealed that potent comutagenic activity of o-vanillin in mutagenesis by N-methyl-N-nitrosourea (MNU) is a consequence of inhibition of the transcriptional promoting capacity of methylated O6-methylguanine-DNA methyltransferase (MGTase). As evidence of this, in the presence of o-vanillin, there were (i) dose-dependent decreases in MGTase induced in E. coli exposed to MNU, (ii) inhibition of ada gene promotion determined in the ada'-lacZ' assay system, and (iii) minimal inhibition of the methyl transfer capacity of MGTase in a subcellular system.
本研究表明,邻香草醛在N-甲基-N-亚硝基脲(MNU)诱变中具有强大的共诱变活性,这是抑制甲基化的O6-甲基鸟嘌呤-DNA甲基转移酶(MGTase)转录促进能力的结果。作为对此的证据,在邻香草醛存在的情况下,有以下情况:(i)暴露于MNU的大肠杆菌中诱导的MGTase呈剂量依赖性降低;(ii)在ada'-lacZ'检测系统中测定的ada基因促进受到抑制;(iii)在亚细胞系统中MGTase的甲基转移能力受到最小程度的抑制。