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PMID: 17853883 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

DNA methylation analysis by pyrosequencing.

Nature protocols ·Vol. 2 ·No. 9 ·2007-00-00 ·Pages 2265-75

Tost J, Gut IG

Abstract

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.

MeSH Terms
Adaptor Proteins, Signal Transducing/chemistry,metabolism Base Composition CpG Islands DNA Methylation Genomic Imprinting Humans MutL Protein Homolog 1 Nuclear Proteins/chemistry,metabolism Polymerase Chain Reaction Sequence Analysis, DNA/methods Sulfites/chemistry
Chemicals
Adaptor Proteins, Signal Transducing MLH1 protein, human Nuclear Proteins Sulfites MutL Protein Homolog 1 hydrogen sulfite
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tost Jörg
Laboratory for Epigenetics, CEA-Institut de Génomique, Centre National de Génotypage, Evry Cedex, France. [email protected]
Gut Ivo G
Article Info
Journal
Nature protocols
Abbr.
Nat Protoc
ISSN
1750-2799
Published
2007-00-00
Pages
2265-75
Language
English
Region
England
NLM ID
101284307
Subset
IM
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