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A Novel CpG Island Set Identifies Tissue-Specific Methylation at Developmental Gene Loci

机译:一种新型的CpG岛集确定发育基因位点的组织特异性甲基化。

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摘要

CpG islands (CGIs) are dense clusters of CpG sequences that punctuate the CpG-deficient human genome and associate with many gene promoters. As CGIs also differ from bulk chromosomal DNA by their frequent lack of cytosine methylation, we devised a CGI enrichment method based on nonmethylated CpG affinity chromatography. The resulting library was sequenced to define a novel human blood CGI set that includes many that are not detected by current algorithms. Approximately half of CGIs were associated with annotated gene transcription start sites, the remainder being intra- or intergenic. Using an array representing over 17,000 CGIs, we established that 6%–8% of CGIs are methylated in genomic DNA of human blood, brain, muscle, and spleen. Inter- and intragenic CGIs are preferentially susceptible to methylation. CGIs showing tissue-specific methylation were overrepresented at numerous genetic loci that are essential for development, including HOX and PAX family members. The findings enable a comprehensive analysis of the roles played by CGI methylation in normal and diseased human tissues.
机译:CpG岛(CGI)是CpG序列的密集簇,可刺穿CpG缺陷型人类基因组并与许多基因启动子相关。由于CGI也因其经常缺乏胞嘧啶甲基化而与体染色体DNA不同,因此我们设计了一种基于非甲基化CpG亲和色谱的CGI富集方法。对得到的文库进行测序,以定义一种新颖的人类血液CGI集,其中包括许多当前算法无法检测到的CGI集。大约一半的CGI与注释的基因转录起始位点相关,其余的是基因内或基因间的。使用代表17,000多个CGI的阵列,我们确定了6%–8%的CGI在人类血液,大脑,肌肉和脾脏的基因组DNA中被甲基化。基因间和基因内的CGI优先受到甲基化的影响。显示组织特异性甲基化的CGI在许多对发育至关重要的遗传基因位点(包括HOX和PAX家族成员)中过分代表。这些发现能够全面分析CGI甲基化在正常和患病人体组织中所起的作用。

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