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胞嘧啶甲基化的比较同裂酶分析:HELP 分析

Comparative isoschizomer profiling of cytosine methylation: the HELP assay.

作者信息

Khulan Batbayar, Thompson Reid F, Ye Kenny, Fazzari Melissa J, Suzuki Masako, Stasiek Edyta, Figueroa Maria E, Glass Jacob L, Chen Quan, Montagna Cristina, Hatchwell Eli, Selzer Rebecca R, Richmond Todd A, Green Roland D, Melnick Ari, Greally John M

机构信息

Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Genome Res. 2006 Aug;16(8):1046-55. doi: 10.1101/gr.5273806. Epub 2006 Jun 29.

Abstract

The distribution of cytosine methylation in 6.2 Mb of the mouse genome was tested using cohybridization of genomic representations from a methylation-sensitive restriction enzyme and its methylation-insensitive isoschizomer. This assay, termed HELP (HpaII tiny fragment Enrichment by Ligation-mediated PCR), allows both intragenomic profiling and intergenomic comparisons of cytosine methylation. The intragenomic profile shows most of the genome to be contiguous methylated sequence with occasional clusters of hypomethylated loci, usually but not exclusively at promoters and CpG islands. Intergenomic comparison found marked differences in cytosine methylation between spermatogenic and brain cells, identifying 223 new candidate tissue-specific differentially methylated regions (T-DMRs). Bisulfite pyrosequencing confirmed the four candidates tested to be T-DMRs, while quantitative RT-PCR for two genes with T-DMRs located at their promoters showed the HELP data to be correlated with gene activity at these loci. The HELP assay is robust, quantitative, and accurate and is providing new insights into the distribution and dynamic nature of cytosine methylation in the genome.

摘要

利用来自甲基化敏感限制酶及其甲基化不敏感同裂酶的基因组代表性片段的共杂交,检测了小鼠基因组6.2 Mb区域内胞嘧啶甲基化的分布情况。这种检测方法称为HELP(通过连接介导的PCR富集HpaII小片段),可同时进行胞嘧啶甲基化的基因组内分析和基因组间比较。基因组内分析显示,基因组的大部分区域为连续的甲基化序列,偶尔会出现低甲基化位点簇,这些位点通常(但并非仅)位于启动子和CpG岛。基因组间比较发现,生精细胞和脑细胞之间的胞嘧啶甲基化存在显著差异,鉴定出223个新的候选组织特异性差异甲基化区域(T-DMR)。亚硫酸氢盐焦磷酸测序证实,所检测的4个候选区域为T-DMR,而对两个启动子区域含有T-DMR的基因进行定量RT-PCR分析表明,HELP检测数据与这些位点的基因活性相关。HELP检测方法具有稳健性、定量性和准确性,为深入了解基因组中胞嘧啶甲基化的分布和动态性质提供了新的视角。

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