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首页> 外文期刊>Methods and Protocols >Estimation of the Mutagenic Potential of 8-Oxog in Nuclear Extracts of Mouse Cells Using the “Framed Mirror” Method
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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:使用“框架镜”法估计小鼠细胞核提取物核提取物的诱变电位

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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 EcoRI 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前面描述的“镜子”方法,用于检测在其复制期间在DNA中产生的细胞核提取物突变,由于脱氧腺苷-5'-单磷酸酯(潮湿)对面的7,8-二氢-8-氧代(8 -oxog)。 该方法基于通过在3'末端含有8- oxog和二赤氧基胞苷残基(DDC)的模板上的不同小鼠器官的核提取物的互补链(“镜子”)的合成。 通过PCR使用底漆部分扩增“镜子”,其与模板不互补。 它允许获得“框架镜子”产品。 “框架镜子”产品中潮湿的MISCLONATION构成了一个ECORI限制性部位。 双链“框架”产品的限制分析允许定量核提取物中的突变频率。 获得的数据表明,8-氧的致致诱变电位明显不同于成人小鼠和胚胎的不同器官。

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