首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Detection of single-strand breaks and formamidopyrimidine-DNA glycosylase-sensitive sites in DNA of cultured human fibroblasts.
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Detection of single-strand breaks and formamidopyrimidine-DNA glycosylase-sensitive sites in DNA of cultured human fibroblasts.

机译:检测培养的人成纤维细胞DNA中的单链断裂和甲酰胺基嘧啶-DNA糖基化酶敏感位点。

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摘要

Under oxidative stress 7,8-dihydro-8-oxo-2'-deoxyguanosine (8-oxodG), a damaged base with mutagenic potential, and single-strand breaks (SSB) are formed in DNA. Both lesions are frequently used as a parameter for oxidative damage of DNA. Here we report on results from the evaluation of a modified nick translation assay, where 8-oxodG and SSB formation in cellular DNA of cultured human fibroblasts were simultaneously detected. The assay is based on a method previously described by others, with several modifications in reaction conditions and type of substrate. We used formamidopyrimidine-DNA glycosylase (FPG) in our assay in order to measure the formation of FPG-sensitive lesions (which include 8-oxodG) in DNA of human fibroblasts in response to ionising radiation. The quantification of the DNA damage was based on calibration experiments with plasmid DNA pUC19. Dose-response curves of SSB and FPG-sensitive lesion formation in human fibroblasts VH-10 were established. A very low background level of 8-oxodG was detected in unirradiated fibroblasts (approx. 500 residues per cell).
机译:在氧化应激下7,8-二氢-8-氧代2'-脱氧鸟苷(8-oxodG)在DNA中形成具有诱变电位的受损碱基和单链断裂(SSB)。两种病变常被用作DNA氧化损伤的参数。在这里,我们报告了从改进的切口平移测定法评估的结果,其中同时检测到培养的人成纤维细胞的细胞DNA中的8-oxodG和SSB形成。该测定基于其他人先前描述的方法,对反应条件和底物类型进行了一些修改。为了测定电离辐射对人成纤维细胞DNA中FPG敏感病变(包括8-oxodG)的形成,我们在测定中使用了甲酰嘧啶-DNA糖基化酶(FPG)。 DNA损伤的定量基于质粒DNA pUC19的校准实验。建立了人成纤维细胞VH-10中SSB和FPG敏感病变形成的剂量反应曲线。在未辐照的成纤维细胞中检测到非常低的8-oxodG背景水平(每个细胞约500个残基)。

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