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Droplet Array Platform for High-Resolution Melt Analysis of DNA Methylation Density

机译:液滴阵列平台,用于DNA甲基化密度的高分辨率熔解分析

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摘要

High-resolution melting (HRM) has garnered significant interest as an analytical technique for a number of applications, including DNA methylation detection, due to its inherent sensitivity and robustness. In this study, we describe a miniaturized assay platform for quantitative methylation density analysis using a microfluidic droplet array cartridge. We demonstrate that the DNA methylation level of the RASSFIA promoter can be directly analyzed using HRM. PCR products were generated by amplifying bisulfite-treated DNA with varying CpG densities using CpG island-flanking primer sets. Subsequent HRM analysis on the miniaturized droplet platform shows distinct melting curve profiles associated with methylation levels, which was verified using a conventional benchtop PCR-HRM system. The characteristic melting temperature (Tm) of the PCR products was used to directly quantify the respective levels of DNA methylation density. Our approach provides a key advantage over current gold standard methods such as methylation-specific PCR (MSP), which are incapable of providing specific information regarding the overall methylation density of the target genes. The miniaturized platform establishes a practical approach to methylation density profiling from multiple DNA samples with a potential application in point-of-care diagnostics.
机译:高分辨率熔解(HRM)由于其固有的灵敏度和鲁棒性,已成为包括DNA甲基化检测在内的许多应用的分析技术,引起了广泛的关注。在这项研究中,我们描述了使用微流控微滴阵列盒进行甲基化密度定量分析的小型化分析平台。我们证明,可以使用HRM直接分析RASSFIA启动子的DNA甲基化水平。 PCR产物是通过使用CpG岛侧翼引物组扩增具有不同CpG密度的亚硫酸氢盐处理的DNA产生的。随后在微型液滴平台上进行的HRM分析显示了与甲基化水平相关的独特熔解曲线图,已使用常规台式PCR-HRM系统进行了验证。 PCR产物的特征解链温度(Tm)用于直接定量DNA甲基化密度的相应水平。与当前的金标准方法(例如甲基化特异性PCR(MSP))相比,我们的方法具有关键优势,因为该方法无法提供有关靶基因总体甲基化密度的特定信息。小型化平台为从多个DNA样本进行甲基化密度分析提供了一种实用的方法,并有望在即时诊断中应用。

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