Allele-specific extension on microarray for DNA methylation analysis

被引:3
|
作者
Wu, Zhixiang
Luo, Junfeng
Ge, Qinyu
Zhang, Dingdong
Wang, Yan
Jia, Chao
Lu, Zuhong
机构
[1] SE Univ, State Key Lab Bioelectron, Nanjing 210096, Peoples R China
[2] SE Univ, Minist Educ, Key Lab Child Dev & Learning Sci, Nanjing 210096, Peoples R China
基金
中国国家自然科学基金;
关键词
methylation; microarray; allele-specific extension; methylation-specific PCR;
D O I
10.1016/j.aca.2007.09.027
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Aberrant DNA methylation of CpG site in the gene promoter region has been confirmed to be closely associated with carcinogenesis. In this present study, a new method based on the allele-specific extension on microarray technique for detecting changes of DNA methylation in cancer was developed. The target gene regions were amplified from the bisulfite treated genomic DNA (gDNA) with modified primers and treated with exonuclease to generate single-strand targets. Allele-specific extension of the immobilized primers took place along a stretch of target sequence with the presence of DNA polymerase and CyS-labeled dGTP. To control the false positive signals, the hybridization condition, DNA polymerase, extension time and primers design were optimized. Two breast tumor-related genes (P16 and E-cadherin) were analyzed with this present method successfully and all the results were compatible with that of traditional methylation-specific PCR. The experiments results demonstrated that this DNA microarray-based method could be applied as a high throughput tool for methylation status analysis of the cancer-related genes, which could be widely used in cancer diagnosis or the detection of recurrence. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 204
页数:6
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