亚硫酸氢盐
亚硫酸氢盐测序
甲基化DNA免疫沉淀
DNA甲基化
分子生物学
底漆(化妆品)
甲基化
生物
照明菌甲基化试验
限制性酶
底漆二聚体
DNA
CpG站点
聚合酶链反应
生物化学
化学
多重聚合酶链反应
基因
基因表达
有机化学
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2006-09-07
卷期号:336: 33-44
被引量:20
标识
DOI:10.1385/1-59745-074-x:33
摘要
DNA methylation can be analyzed easily by qualitative or quantitative polymerase chain reaction (PCR)-based methods, including methylation-specific PCR (MSP), bisulfite sequencing, methylation-sensitive restriction enzyme PCR, combined bisulfite restriction analysis (COBRA), methylation-sensitive single nucleotide primer extension (Ms-SNuPE), and quantitative real-time MSP. MSP, which couples the bisulfite modification of DNA and PCR, is fast, highly sensitive, specific, and widely applied for DNA methylation analyses. Bisulfite modification converts unmethylated cytosine to uracil, whereas methylcytosine remains unmodified. Most of these methods require specific PCR primers that are designed to distinguish between methylated and unmethylated DNA sequences. Bisulfite sequencing is comparatively time-consuming. Methylation-sensitive restriction enzyme PCR combines methylation-sensitive restriction enzyme digestion and PCR. After enzyme digestion, PCR products are obtained if the enzyme does not digest the methylated CpG sites within the specified DNA region. COBRA, Ms-SNuPE, and quantitative real-time MSP allow the quantitative analyses of DNA methylation.
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