Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.
Int J Mol Sci. 2024 May 7;25(10):5082. doi: 10.3390/ijms25105082.
High-resolution melting (HRM) is a cost-efficient tool for targeted DNA methylation analysis. HRM yields the average methylation status across all CpGs in PCR products. Moreover, it provides information on the methylation pattern, e.g., the occurrence of monoallelic methylation. HRM assays have to be calibrated by analyzing DNA methylation standards of known methylation status and mixtures thereof. In general, DNA methylation levels determined by the classical calibration approach, including the whole temperature range in between normalization intervals, are in good agreement with the mean of the DNA methylation status of individual CpGs determined by pyrosequencing (PSQ), the gold standard of targeted DNA methylation analysis. However, the classical calibration approach leads to highly inaccurate results for samples with heterogeneous DNA methylation since they result in more complex melt curves, differing in their shape compared to those of DNA standards and mixtures thereof. Here, we present a novel calibration approach, i.e., temperature-wise calibration. By temperature-wise calibration, methylation profiles over temperature are obtained, which help in finding the optimal calibration range and thus increase the accuracy of HRM data, particularly for heterogeneous DNA methylation. For explaining the principle and demonstrating the potential of the novel calibration approach, we selected the promoter and two enhancers of , a gene encoding the repair protein MGMT.
高分辨率熔解(HRM)是一种用于靶向 DNA 甲基化分析的经济高效的工具。HRM 可提供 PCR 产物中所有 CpG 的平均甲基化状态。此外,它还提供有关甲基化模式的信息,例如单等位基因甲基化的发生情况。HRM 分析必须通过分析具有已知甲基化状态的 DNA 甲基化标准品及其混合物来进行校准。一般来说,通过经典校准方法确定的 DNA 甲基化水平,包括在标准化间隔之间的整个温度范围内,与通过焦磷酸测序(PSQ)确定的单个 CpG 的 DNA 甲基化状态的平均值非常吻合,PSQ 是靶向 DNA 甲基化分析的金标准。然而,经典的校准方法对于具有异质 DNA 甲基化的样本会导致非常不准确的结果,因为它们会导致更复杂的熔解曲线,与 DNA 标准品及其混合物的形状不同。在这里,我们提出了一种新的校准方法,即温度校准。通过温度校准,可以获得温度范围内的甲基化谱,这有助于找到最佳的校准范围,从而提高 HRM 数据的准确性,特别是对于异质 DNA 甲基化。为了解释新校准方法的原理并展示其潜力,我们选择了编码修复蛋白 MGMT 的基因的启动子和两个增强子。