Brozmanova J, Kleibl K, Vlckova V, Skorvaga M, Cernakova L, Margison G P
Cancer Research Institute, Slovak Academy of Sciences, Bratislava.
Nucleic Acids Res. 1990 Jan 25;18(2):331-5. doi: 10.1093/nar/18.2.331.
The E.coli ada gene protein coding region has been ligated into an extrachromosomally replicating yeast expression vector downstream of the yeast alcohol dehydrogenase gene promoter region to produce pADH06C. The yeast strains SX46A, 7799-4B and VV-6 are deficient in endogenous O6-alkylguanine-DNA-alkyltransferase and transformation of these strains with this shuttle vector resulted in the expression of 1730, 1260 and 374 fmoles ada-encoded ATase/mg protein in stationary phase yeast: transformation with the parent vector had no effect on endogenous ATase activity which remained less than 2 fm/mg. In comparison with parent vector transformed yeast, all of the pADH06C-transformed strains showed an increase in the resistance to the toxic effects of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). In addition, 7799-4B and VV-6 were more resistant to the mutagenic effects of this agent. These results indicate that the toxic and mutagenic effects of MNNG in yeast are mediated, at least in part, by DNA lesions than can be repaired by the E.coli ada gene product.
大肠杆菌ada基因的蛋白质编码区已被连接到酵母乙醇脱氢酶基因启动子区域下游的一种染色体外复制的酵母表达载体中,以产生pADH06C。酵母菌株SX46A、7799 - 4B和VV - 6缺乏内源性O6 - 烷基鸟嘌呤 - DNA - 烷基转移酶,用这种穿梭载体转化这些菌株后,在稳定期酵母中分别产生了1730、1260和374飞摩尔ada编码的烷基转移酶/毫克蛋白质:用亲本载体转化对内源性烷基转移酶活性没有影响,其仍低于2飞摩尔/毫克。与亲本载体转化的酵母相比,所有pADH06C转化的菌株对N - 甲基 - N' - 硝基 - N - 亚硝基胍(MNNG)的毒性作用的抗性都有所增加。此外,7799 - 4B和VV - 6对该试剂的诱变作用更具抗性。这些结果表明,MNNG在酵母中的毒性和诱变作用至少部分是由可被大肠杆菌ada基因产物修复的DNA损伤介导的。