首页> 美国卫生研究院文献>Nucleic Acids Research >Reduction of the toxicity and mutagenicity of aziridine in mammalian cells harboring the Escherichia coli fpg gene.
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Reduction of the toxicity and mutagenicity of aziridine in mammalian cells harboring the Escherichia coli fpg gene.

机译:减少氮丙啶在含有大肠杆菌fpg基因的哺乳动物细胞中的毒性和致突变性。

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摘要

Aziridine (ethyleneimine) reacts with DNA in vitro, mainly at the N7 position of guanine and N3 of adenine, then imidazole ring opening of the modified guanine results in formation of formamidopyrimidine (FaPy) residues. The Escherichia coli fpg gene encodes a DNA glycosylase that removes FaPy residues from DNA. To determine whether aziridine produces FaPy lesions in mammalian cells we have expressed the E.coli fpg gene in CHO cells. The transfected cells, expressing high levels of the bacterial protein, are more resistant to the toxic and mutagenic effects of aziridine than the control population. Less DNA damage was measured by quantitative PCR analysis in transfected than in control cells treated with equimolar concentrations of aziridine. The results suggest that aziridine produces in vivo FaPy residues that could account for the deleterious effects of this compound.
机译:氮丙啶(乙烯亚胺)在体外与DNA反应,主要在鸟嘌呤的N7位置和腺嘌呤的N3,然后修饰的鸟嘌呤的咪唑开环导致形成甲酰嘧啶(FaPy)残基。大肠杆菌fpg基因编码一种DNA糖基化酶,可从DNA中去除FaPy残基。为了确定氮丙啶在哺乳动物细胞中是否产生FaPy损伤,我们已经在CHO细胞中表达了大肠杆菌fpg基因。表达高水平细菌蛋白的转染细胞,与对照组相比,对氮丙啶的毒性和诱变作用更具抵抗力。通过定量PCR分析,与等摩尔浓度的氮丙啶处理的对照细胞相比,通过定量PCR分析测得的DNA损伤更少。结果表明,氮丙啶在体内产生FaPy残基,这可能解释了该化合物的有害作用。

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