DNA methylation analysis by pyrosequencing

被引:501
作者
Tost, Joeg [1 ]
Gut, Ivo G. [2 ]
机构
[1] CEA, Inst Genom, Ctr Natl Genotypage, Lab Epigenet, F-91057 Evry, France
[2] CEA, Inst Genom, Ctr Natl Genotypage, Dept Technol Dev, F-91057 Evry, France
关键词
D O I
10.1038/nprot.2007.314
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pyrosequencing is a sequencing-by-synthesis method that quantitatively monitors the real-time incorporation of nucleotides through the enzymatic conversion of released pyrophosphate into a proportional light signal. Quantitative measures are of special importance for DNA methylation analysis in various developmental and pathological situations. Analysis of DNA methylation patterns by pyrosequencing combines a simple reaction protocol with reproducible and accurate measures of the degree of methylation at several CpGs in close proximity with high quantitative resolution. After bisulfite treatment and PCR, the degree of each methylation at each CpG position in a sequence is determined from the ratio of T and C. The process of purification and sequencing can be repeated for the same template to analyze other CpGs in the same amplification product. Quantitative epigenotypes are obtained using this protocol in approximately 4 h for up to 96 DNA samples when bisulfite-treated DNA is already available as the starting material.
引用
收藏
页码:2265 / 2275
页数:11
相关论文
共 39 条
[1]   The BiSearch web server [J].
Aranyi, Tamas ;
Varadi, Andras ;
Simon, Istvan ;
Tusnady, Gabor E. .
BMC BIOINFORMATICS, 2006, 7 (1)
[2]   Promoter methylation analysis on micro-dissected paraffin-embedded tissues using bisulfite treatment and PCR-SSCP [J].
Bian, YS ;
Yan, P ;
Osterheld, MC ;
Fontolliet, C ;
Benhattar, J .
BIOTECHNIQUES, 2001, 30 (01) :66-+
[3]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[4]   Bisulfite conversion of genomic DNA for methylation analysis: protocol simplification with higher recovery applicable to limited samples and increased throughput [J].
Boyd, VL ;
Zon, G .
ANALYTICAL BIOCHEMISTRY, 2004, 326 (02) :278-280
[5]   Quantitative assessment of DNA methylation: potential applications for disease diagnosis, classification, and prognosis in clinical settings [J].
Brena, Romulo Martin ;
Huang, Tim Hui-Ming ;
Plass, Christoph .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2006, 84 (05) :365-377
[6]   Pyrosequencing: nucleotide sequencing technology with bacterial genotyping applications [J].
Clarke, SC .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (06) :947-953
[7]   Sensitive and quantitative universal Pyrosequencing™ methylation analysis of CpG sites [J].
Colella, S ;
Shen, L ;
Baggerly, KA ;
Issa, JPJ ;
Krahe, R .
BIOTECHNIQUES, 2003, 35 (01) :146-+
[8]   Detection of aneuploidies by paralogous sequence quantification [J].
Deutsch, S ;
Choudhury, U ;
Merla, G ;
Howald, C ;
Sylvan, A ;
Antonarakis, SE .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (12) :908-915
[9]   De novo quantitative bisulfite sequencing using the pyrosequencing technology [J].
Dupont, JM ;
Tost, J ;
Jammes, H ;
Gut, NG .
ANALYTICAL BIOCHEMISTRY, 2004, 333 (01) :119-127
[10]   Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry [J].
Ehrich, M ;
Nelson, MR ;
Stanssens, P ;
Zabeau, M ;
Liloglou, T ;
Xinarianos, G ;
Cantor, CR ;
Field, JK ;
van den Boom, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (44) :15785-15790