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Estimation of the Mutagenic Potential of 8-Oxog in Nuclear Extracts of Mouse Cells Using the Framed Mirror Method

机译:用镜框镜法估算小鼠细胞核提取物中8-氧合蛋白的致突变潜力

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摘要

We propose an improved earlier described “mirror” method for detecting in cell nuclear extracts mutations that arise in DNA during its replication due to the misincorporation of deoxyadenosine-5′-monophosphate (dAMP) opposite 7,8-dihydro-8-oxoguanine (8-oxoG). This method is based on the synthesis of a complementary chain (“mirror”) by nuclear extracts of different mice organs on a template containing 8-oxoG and dideoxycytidine residue (ddC) at the 3′‑end. The “mirror” was amplified by PCR using primers part of which was non-complementary to the template. It allowed obtaining the “framed mirror” products. The misincorporation of dAMP in “framed mirror” products forms an restriction site. The restriction analysis of double-stranded “framed mirror” products allows a quantification of the mutation frequency in nuclear extracts. The data obtained show that the mutagenic potential of 8-oxoG markedly varied in different organs of adult mice and embryos.
机译:我们提出了一种改进的较早描述的“镜像”方法,用于检测DNA复制过程中由于脱氧腺苷-5'-单磷酸(dAMP)与7,8-二氢-8-氧鸟嘌呤相对而错误掺入而引起的DNA突变(8 -oxoG)。此方法基于在3'端含有8-oxoG和双脱氧胞苷残基(ddC)的模板上不同小鼠器官的核提取物合成的互补链(“镜像”)。通过使用部分引物与模板不互补的引物通过PCR扩增“镜子”。它允许获得“镜框”产品。 dAMP在“镜框”产品中的错误掺入形成限制位点。对双链“镜框”产品的限制性分析可以定量核提取物中的突变频率。获得的数据表明,在成年小鼠和胚胎的不同器官中,8-oxoG的诱变潜力明显不同。

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