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过氧化氢可诱导大肠杆菌supF基因中发生从G:C到T:A以及从G:C到C:G的颠换。

Hydrogen peroxide induces G:C to T:A and G:C to C:G transversions in the supF gene of Escherichia coli.

作者信息

Akasaka S, Yamamoto K

机构信息

Division of Industrial Health, Osaka Prefectural Institute of Public Health, Japan.

出版信息

Mol Gen Genet. 1994 Jun 3;243(5):500-5. doi: 10.1007/BF00284197.

DOI:10.1007/BF00284197
PMID:8208241
Abstract

A vector plasmid, pZ189, carrying an Escherichia coli supF gene as a target for mutations, was treated with a combination of hydrogen peroxide and Fe3+/EDTA complex and propagated in E. coli host cells that had been induced for SOS functions by ultraviolet irradiation. The mutations frequency increased by up to 30-fold over spontaneous background levels with increasing concentrations of hydrogen peroxide. The increase in mutation frequency correlated with an increase in the formation of 8-hydroxydeoxyguanosine in the pZ189 DNA. Sequence analysis of 82 independent supF mutant plasmids revealed that 70 mutants contained base substitutions, with 63 of the 70 involving a G:C base pair, and with G:C-->C:G (28 cases) and G:C-->T:A (26 cases) transversions predominating. Investigation of the influence of the local DNA sequence on the transversions revealed that the guanine at the center of the triplet 5'-PuGA-3' was five times more likely to mutate after treatment with hydrogen peroxide than that at the center of 5'PyGN3'. G:C-->T:A transversions presumably resulted from mispairing of an altered G (probably 8-hydroxydeoxyguanosine) with deoxyadenosine. The origin of the G:C-->C:G transversions may be an as yet unidentified lesion generated by hydrogen peroxide. Mutagenic hotspots for base substitutions were found at positions 133, 160 and 168. Mutation spectra and the positions of mutagenic hotspots, when compared with a previously determined spontaneous mutagenesis spectrum, also provide information on the mechanism of spontaneous mutagenesis.

摘要

携带大肠杆菌supF基因作为突变靶点的载体质粒pZ189,用过氧化氢和Fe3+/EDTA复合物处理,并在经紫外线照射诱导SOS功能的大肠杆菌宿主细胞中增殖。随着过氧化氢浓度的增加,突变频率比自发背景水平增加了30倍。突变频率的增加与pZ189 DNA中8-羟基脱氧鸟苷的形成增加相关。对82个独立的supF突变体质粒进行序列分析,发现70个突变体含有碱基替换,其中70个中的63个涉及G:C碱基对,且G:C→C:G(28例)和G:C→T:A(26例)颠换占主导。对局部DNA序列对颠换影响的研究表明,三联体5'-PuGA-3'中心的鸟嘌呤在用过氧化氢处理后发生突变的可能性是5'PyGN3'中心鸟嘌呤的5倍。G:C→T:A颠换可能是由改变的G(可能是8-羟基脱氧鸟苷)与脱氧腺苷错配导致的。G:C→C:G颠换的起源可能是过氧化氢产生的一种尚未确定的损伤。在第133、160和168位发现了碱基替换的诱变热点。与先前确定的自发诱变谱相比,突变谱和诱变热点的位置也提供了关于自发诱变机制的信息。

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