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Open AccessMethodology article

A novel method to quantify local CpG methylation density by regional methylation elongation assay on microarray

Dingdong Zhang1,2* email, Yan Wang1* email, Yunfei Bai1 email, Qinyu Ge1 email, Yingjuan Qiao1 email, Junfeng Luo1 email, Chao Jia1 email and Zuhong Lu1 email

State Key Laboratory of Bioelectronics, Southeast University, Nanjing 210096, China

College of Animal Science and Technology, Jinling Institute of Technology, Nanjing 210038, China

author email corresponding author email* Contributed equally

BMC Genomics 2008, 9:59doi:10.1186/1471-2164-9-59

Published: 31 January 2008

Abstract

Background

DNA methylation based techniques are important tools in both clinical diagnostics and therapeutics. But most of these methods only analyze a few CpG sites in a target region. Indeed, difference of site-specific methylation may also lead to a change of methylation density in many cases, and it has been found that the density of methylation is more important than methylation of single CpG site for gene silencing.

Results

We have developed a novel approach for quantitative analysis of CpG methylation density on the basis of microarray-based hybridization and incorporation of Cy5-dCTP into the Cy3 labeled target DNA by using Taq DNA Polymerase on microarray. The quantification is achieved by measuring Cy5/Cy3 signal ratio which is proportional to methylation density. This methylation-sensitive technique, termed RMEAM (regional methylation elongation assay on microarray), provides several advantages over existing methods used for methylation analysis. It can determine an exact methylation density of the given region, and has potential of high throughput. We demonstrate a use of this method in determining the methylation density of the promoter region of the tumor-related gene MLH1, TERT and MGMT in colorectal carcinoma patients.

Conclusion

This technique allows for quantitative analysis of regional methylation density, which is the representative of all allelic methylation patterns in the sample. The results show that this technique has the characteristics of simplicity, rapidness, specificity and high-throughput.


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