A Modified and Improved Method for Bisulphite Based Cytosine Methylation Analysis
Author(s) -
Alexander Olek,
Joachim Oswald,
Jörn Walter
Publication year - 1996
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/24.24.5064
Subject(s) - bisulfite sequencing , biology , dna methylation , dna , agarose , bisulfite , cytosine , computational biology , methylation , dna sequencing , sensitivity (control systems) , microbiology and biotechnology , genetics , gene , gene expression , electronic engineering , engineering
Sequencing of bisulphite modified genomic DNA is the most powerful method to determine methylation patterns in chromosomal DNA. In many experimental systems, the amount of material available for analysis is very small which makes it necessary to perform experiments at extreme levels of sensitivity and reproducibility. In this communication, we present an improved modification of the bisulphite based sequencing method. Our strategy is to perform the bisulphite treatment and subsequent PCR steps on material embedded into agarose beads. This prevents loss of DNA during the experimental procedure and ensures an optimal bisulphite reactivity by maintaining the DNA in the single stranded form. The modification improves previously published protocols in that it facilitates the handling of probes and reproducibly reaches a very high level of sensitivity.
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