Optimizing methodologies for PCR-based DNA methylation analysis

被引:129
|
作者
Hernandez, Hernan G. [1 ,2 ,3 ]
Tse, M. Yat [4 ]
Pang, Stephen C. [4 ]
Arboleda, Humberto [2 ]
Forero, Diego A. [1 ]
机构
[1] Univ Antonio Narino, Lab NeuroPsychiat Genet, Biomed Sci Res Grp, Sch Med, Bogota, Colombia
[2] Univ Nacl Colombia, Neurosci Res Grp, Sch Med, Bogota, Colombia
[3] Univ Nacl Colombia, Biomed Sci Doctoral Program, Sch Med, Bogota, Colombia
[4] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON, Canada
关键词
epigenomics; DNA methylation; MS-HRM; MethyLight; 5-methylcytosine; polymerase chain reaction; reference standards; POLYMERASE-CHAIN-REACTION; PERIPHERAL-BLOOD DNA; PROMOTER METHYLATION; HIGH-THROUGHPUT; PRIMER-DESIGN; BISULFITE MODIFICATION; WEB-TOOLS; RESOLUTION; CANCER; GENOME;
D O I
10.2144/000114087
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Comprehensive analysis of DNA methylation patterns is critical for understanding the molecular basis of many human diseases. While hundreds of PCR-based DNA methylation studies are published every year, the selection and implementation of appropriate methods for these studies can be challenging for molecular genetics researchers not yet familiar with methylation analysis. Here we review the most commonly used PCR-based DNA methylation analysis techniques: bisulfite sequencing PCR (BSP), methylation specific PCR (MSP), MethyLight, and methylation-sensitive high resolution melting (MS-HRM). We provide critical analysis of the strengths and weaknesses of each approach as well as a series of guidelines to assist in selecting and implementing an appropriate method.
引用
收藏
页码:181 / 197
页数:17
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