Department of Forensic medicine, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Rd, Wuhan, 430030, China.
BMC Mol Biol. 2017 Dec 19;18(1):24. doi: 10.1186/s12867-017-0101-4.
Methylation analysis of cell-free DNA is a encouraging tool for tumor diagnosis, monitoring and prognosis. Sensitivity of methylation analysis is a very important matter due to the tiny amounts of cell-free DNA available in plasma. Most current methods of DNA methylation analysis are based on the difference of bisulfite-mediated deamination of cytosine between cytosine and 5-methylcytosine. However, the recovery of bisulfite-converted DNA based on current methods is very poor for the methylation analysis of cell-free DNA.
We optimized a rapid method for the crucial steps of bisulfite conversion with high recovery of cell-free DNA. A rapid deamination step and alkaline desulfonation was combined with the purification of DNA on a silica column. The conversion efficiency and recovery of bisulfite-treated DNA was investigated by the droplet digital PCR. The optimization of the reaction results in complete cytosine conversion in 30 min at 70 °C and about 65% of recovery of bisulfite-treated cell-free DNA, which is higher than current methods.
The method allows high recovery from low levels of bisulfite-treated cell-free DNA, enhancing the analysis sensitivity of methylation detection from cell-free DNA.
游离 DNA 的甲基化分析是一种很有前途的肿瘤诊断、监测和预后工具。由于血浆中游离 DNA 含量极少,因此甲基化分析的灵敏度是一个非常重要的问题。目前大多数 DNA 甲基化分析方法都是基于亚硫酸氢盐介导的胞嘧啶与 5-甲基胞嘧啶之间脱氨反应的差异。然而,目前的方法对于游离 DNA 的甲基化分析,其对亚硫酸氢盐转化 DNA 的回收效果很差。
我们优化了一种快速的方法,用于关键的亚硫酸氢盐转化步骤,以实现高回收率的游离 DNA。快速脱氨步骤和碱性脱硫与硅基柱上的 DNA 纯化相结合。通过液滴数字 PCR 研究了亚硫酸氢盐处理的 DNA 的转化率和回收率。反应的优化结果是在 70°C 下 30 分钟内实现完全的胞嘧啶转化,并且大约 65%的亚硫酸氢盐处理的游离 DNA 得到回收,高于目前的方法。
该方法允许从低水平的亚硫酸氢盐处理的游离 DNA 中进行高回收,从而提高了从游离 DNA 中检测甲基化的分析灵敏度。