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亚甲蓝加可见光诱导的lacZ中的非SOS依赖性诱变。

SOS-independent mutagenesis in lacZ induced by methylene blue plus visible light.

作者信息

Tudek B, Laval J, Boiteux S

机构信息

LA147 CNRS, U140 INSERM, Groupe Réparation des lésions radio et chimioinduites, Institut Gustave Roussy, Villejuif, France.

出版信息

Mol Gen Genet. 1993 Jan;236(2-3):433-9. doi: 10.1007/BF00277144.

DOI:10.1007/BF00277144
PMID:8437588
Abstract

In vitro photosensitization by visible light in the presence of methylene blue (MB-light) produces lesions in M13mp18 lacZ phage DNA, the lethal and mutagenic potential of which was analyzed after transfection into various bacterial hosts. Mutagenesis was determined with a forward mutation assay using the lacZ gene of M13mp18 as a target. When, MB-light-treated double-stranded (ds) M13mp18 DNA was used to transfect wild-type cells which were not induced for SOS functions, a fivefold increase in mutation frequency was observed at 10% survival compared to that observed with untreated DNA. Mutation frequency obtained with MB-light-treated ds M13mp18 DNA was greater when transfected into the uvr A fpg-1 double mutant than that seen in uvr A, fpg-1, or umuC single mutants or in the wild-type. Sequence analysis shows that in the wild-type strain, MB-light treatment of ds M13mp18 DNA results mostly in single base substitutions. The most frequent base change is the GC-->TA transversion. MB-light treatment of single-stranded (ss) M13mp18 DNA also results in an increased mutation frequency after transfection into the wild-type strain, yielding mostly G-->T transversions. Our results show that MB-light-induced mutagenesis is at least partially independent of the induction of SOS functions in Escherichia coli. The mutation spectra suggest that 8-oxo-7,8-dihydroguanine is the major promutagenic lesion in DNA.

摘要

在亚甲蓝存在下可见光介导的体外光敏作用(MB-光)会在M13mp18 lacZ噬菌体DNA中产生损伤,在将其转染到各种细菌宿主后分析了其致死和诱变潜力。使用M13mp18的lacZ基因作为靶点,通过正向突变试验确定诱变作用。当用经MB-光处理的双链(ds)M13mp18 DNA转染未诱导SOS功能的野生型细胞时,与未处理的DNA相比,在10%存活率下观察到突变频率增加了五倍。当将经MB-光处理的ds M13mp18 DNA转染到uvr A fpg-1双突变体中时,获得的突变频率高于在uvr A、fpg-1或umuC单突变体或野生型中观察到的频率。序列分析表明,在野生型菌株中,对ds M13mp18 DNA进行MB-光处理主要导致单碱基替换。最常见的碱基变化是GC→TA颠换。对单链(ss)M13mp18 DNA进行MB-光处理后转染到野生型菌株中也会导致突变频率增加,主要产生G→T颠换。我们的结果表明,MB-光诱导的诱变作用至少部分独立于大肠杆菌中SOS功能的诱导。突变谱表明,8-氧代-7,8-二氢鸟嘌呤是DNA中的主要前诱变损伤。

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本文引用的文献

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Cleavage and binding of a DNA fragment containing a single 8-oxoguanine by wild type and mutant FPG proteins.野生型和突变型FPG蛋白对含有单个8-氧代鸟嘌呤的DNA片段的切割与结合
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Hydrogen peroxide induces G:C to T:A and G:C to C:G transversions in the supF gene of Escherichia coli.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。
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从经γ射线辐照的聚脱氧核糖核苷酸中酶促切除其咪唑环已断裂的腺嘌呤残基。
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Mutational specificity of depurination.脱嘌呤的突变特异性
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New M13 vectors for cloning.用于克隆的新型M13载体。
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Proteins required for ultraviolet light and chemical mutagenesis. Identification of the products of the umuC locus of Escherichia coli.紫外线和化学诱变所需的蛋白质。大肠杆菌umuC基因座产物的鉴定。
J Mol Biol. 1983 Feb 25;164(2):175-92. doi: 10.1016/0022-2836(83)90074-8.
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Fidelity of DNA synthesis.DNA合成的保真度。
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Ring-opened 7-methylguanine residues in DNA are a block to in vitro DNA synthesis.DNA中开环的7-甲基鸟嘌呤残基会阻碍体外DNA合成。
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