We report here on a quantitative technique called COBRA to determine DNA methylation levels at specific gene loci in small amounts of genomic DNA. Restriction enzyme digestion is used to reveal methylation-dependent sequence differences in PCR products of sodium bisulfite-treated DNA as described previously. We show that methylation levels in the original DNA sample are represented by the relative amounts of digested and undigested PCR product in a linearly quantitative fashion across a wide spectrum of DNA methylation levels. In addition, we show that this technique can be reliably applied to DNA obtained from microdissected paraffin-embedded tissue samples. COBRA thus combines the powerful features of ease of use, quantitative accuracy, and compatibility with paraffin sections.
COBRA: a sensitive and quantitative DNA methylation assay
Autor(es):
Z Xiong 1, P W Laird
Patologia:
Análise de Metilação de DNA
Link do Artigo:
Acessar Artigo Original
Data de Criação:
16/05/2022
Data de Publicação:
15/06/1997