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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.

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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