Akey Dayna T, Akey Joshua M, Zhang Kun, Jin Li
Center for Genome Information, Department of Environmental Health, University of Cincinnati, Cincinnati, Ohio 45267, USA.
Genomics. 2002 Oct;80(4):376-84. doi: 10.1006/geno.2002.6851.
Here we describe two high-throughput methods to assay DNA methylation, melting curve methylation specific PCR (McMSP) and melting curve combined bisulfite restriction analysis (McCOBRA), which adapt standard MSP and COBRA methods to a melting curve analysis based platform. We show that McMSP and McCOBRA can accurately determine methylation status in a high-throughput and gel-free manner. Moreover, McCOBRA can be used to quantitatively estimate the percent of methylated DNA at a specific CpG site within a heterogeneous sample. The accuracy of McMSP and McCOBRA was initially tested using the 5'-CpG site of the tumor-suppressor gene CDKN2A as a model system in homogeneous and heterogeneous controls, and cancer cell line samples. Furthermore, the robustness of McMSP and McCOBRA was validated in four additional loci. We demonstrate that McCOBRA and McMSP provide several advantages over existing methods, as they are simple, accurate, and high-throughput, which makes them widely applicable to large-scale methylation studies.
在此,我们描述了两种用于检测DNA甲基化的高通量方法,即熔解曲线甲基化特异性PCR(McMSP)和熔解曲线联合亚硫酸氢盐限制性分析(McCOBRA),它们将标准的MSP和COBRA方法应用于基于熔解曲线分析的平台。我们表明,McMSP和McCOBRA能够以高通量且无需凝胶的方式准确确定甲基化状态。此外,McCOBRA可用于定量估计异质样品中特定CpG位点处甲基化DNA的百分比。最初,使用肿瘤抑制基因CDKN2A的5'-CpG位点作为模型系统,在同质和异质对照以及癌细胞系样品中测试了McMSP和McCOBRA的准确性。此外,在另外四个位点验证了McMSP和McCOBRA的稳健性。我们证明,McCOBRA和McMSP相对于现有方法具有多个优点,因为它们简单、准确且高通量,这使得它们广泛适用于大规模甲基化研究。