Figueroa Maria E, Melnick Ari, Greally John M
Department of Medicine and Department of Molecular Genetics, Albert Einstein College of Medicine, 1300 Morris Park Ave., Ullmann 911, Bronx, NY 10461, USA.
Methods Mol Biol. 2009;538:395-407. doi: 10.1007/978-1-59745-418-6_20.
Aberrant distribution of cytosine methylation in cancer has been linked to deregulation of gene expression and genomic instability. DNA methylation changes in cancer include both hyper and hypomethylation, and the precise localization of these changes is directly related to the impact they have on gene regulation. To determine both the localization and extent of DNA methylation status under different conditions, we have developed the HpaII tiny fragment enrichment by ligation-mediated PCR (HELP) assay, a microarray-based technique that allows the simultaneous interrogation of the methylation status of hundreds of thousands of CpG dinucleotides. The HELP assay allows methylation levels throughout the genome to be accurately determined so that the epigenetic state of leukemia cells can be identified, compared, and contrasted.
癌症中胞嘧啶甲基化的异常分布与基因表达失调和基因组不稳定有关。癌症中的DNA甲基化变化包括高甲基化和低甲基化,这些变化的精确定位与它们对基因调控的影响直接相关。为了确定不同条件下DNA甲基化状态的定位和程度,我们开发了连接介导的PCR富集HpaII小片段(HELP)分析法,这是一种基于微阵列的技术,可同时检测数十万CpG二核苷酸的甲基化状态。HELP分析法能够准确测定全基因组的甲基化水平,从而识别、比较和对比白血病细胞的表观遗传状态。