Reid T M, Feig D I, Loeb L A
Joseph Gottstein Memorial Cancer Research Laboratory, Department of Pathology, University of Washington School of Medicine, Seattle 98195.
Environ Health Perspect. 1994 Sep;102 Suppl 3(Suppl 3):57-61. doi: 10.1289/ehp.94102s357.
To assess the contribution of reactive oxygen species (ROS) to metal-induced mutagenesis, we have determined the spectrum of mutations in the lacZ alpha gene after exposure of M13mp2 DNA to Fe2+, Cu2+, and Ni2+. With iron and copper ions, mutations are clustered and are predominantly single-base substitutions. Fe, Cu, and phorbol ester-stimulated neutrophils also produced tandem double CC-->TT mutations. This mutation may provide a marker for the role of oxidative damage in carcinogenesis. Mutagenesis by Ni2+ required the complexing of the metal to a tripeptide and the addition of H2O2. To assess the contribution of ROS in mammalian cells, we determined the spectrum of mutations produced when purified DNA polymerases-alpha and -beta synthesized DNA using a template that had been damaged by ROS. The mutation spectra produced by the two polymerases indicates that these enzymes substitute different nucleotides opposite the same lesions.
为评估活性氧(ROS)对金属诱导诱变的作用,我们测定了M13mp2 DNA暴露于Fe2+、Cu2+和Ni2+后lacZα基因中的突变谱。铁离子和铜离子诱导的突变呈簇状分布,且主要为单碱基替换。铁、铜以及佛波酯刺激的中性粒细胞也会产生串联双CC→TT突变。这种突变可能为氧化损伤在致癌过程中的作用提供一个标志物。Ni2+诱导的诱变需要金属与三肽络合并添加H2O2。为评估ROS在哺乳动物细胞中的作用,我们测定了纯化的DNA聚合酶α和β使用被ROS损伤的模板合成DNA时产生的突变谱。两种聚合酶产生的突变谱表明,这些酶在相同损伤位点对面替换不同的核苷酸。