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Methylation-sensitive high resolution melting (MS-HRM): a new approach for sensitive and high-throughput assessment of methylation

机译:甲基化敏感的高分辨率熔解(MS-HRM):一种用于甲基化的灵敏且高通量评估的新方法

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In this article, we show that high resolution melting analysis (HRM) is a sensitive and specific method for the detection of methylation. Methylated DNA and unmethylated DNA acquire different sequences after bisulphite treatment resulting in PCR products with markedly different melting profiles. We used PCR to amplify both methylated and unmethylated sequences and assessed HRM for the determination of the methylation status of the MGMT promoter region. Reconstruction experiments showed that MGMT methylation could be detected at levels as low as 0.1%. Moreover, MS-HRM allows for estimation of the methylation level by comparing the melting profiles of unknown PCR products to the melting profiles of PCR products derived from standards with a known unmethylated to methylated template ratio. We used MS-HRM for the analysis of eight cell lines of known methylation status and a panel of colorectal cancer specimens. The simplicity and high reproducibility of the MS-HRM protocol makes MS-HRM the method of choice for methylation assessment in many diagnostic and research applications.
机译:在本文中,我们显示了高分辨率熔解分析(HRM)是检测甲基化的灵敏且特异的方法。亚硫酸氢盐处理后,甲基化的DNA和未甲基化的DNA获得不同的序列,导致PCR产物的熔解曲线显着不同。我们使用PCR扩增甲基化和非甲基化序列,并评估HRM以确定MGMT启动子区域的甲基化状态。重建实验表明,MGMT甲基化水平可低至0.1%。此外,MS-HRM可以通过将未知PCR产物的熔解曲线与衍生自具有已知未甲基化与甲基化模板比的标准液的PCR产物的熔解曲线进行比较来估算甲基化水平。我们使用MS-HRM分析了八种已知甲基化状态的细胞系和一组结肠直肠癌标本。 MS-HRM协议的简单性和高可重复性使MS-HRM成为许多诊断和研究应用中甲基化评估的首选方法。

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