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首页> 外文期刊>Human Molecular Genetics >Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns
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Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns

机译:从人体解剖标本中提取的体细胞组织的表观遗传学特征鉴定出组织和个体特异性DNA甲基化模式

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摘要

DNA methylation is known to be associated with cell differentiation, aging, disease and cancer. There exists an expanding base of knowledge regarding tissue-specific DNA methylation, but we have little information about person-specific DNA methylation. Here, we analyze the DNA methylation patterns of multiple tissues from multiple individuals using a high-throughput quantitative assay of genome-wide DNA methylation, namely the Illumina GoldenGate BeadArray. DNA methylation patterns were largely conserved across 11 different tissues (r = 0.852) and across six individuals (r = 0.829), and we found that DNA was highly methylated in non-CpG islands and/or CpG sites that are not occupied by either H3K4me3 or H3K27me3 (P 0.05). Finally, we found that the Illumina GoldenGate assay features a large number of probes (265/1505 probes, 17.6%) that contain single-nucleotide polymorphisms, which may interfere with DNA methylation analyses in genome-wide studies.
机译:已知DNA甲基化与细胞分化,衰老,疾病和癌症有关。关于组织特异性DNA甲基化的知识已有不断扩展的知识,但是关于人特异性DNA甲基化的信息很少。在这里,我们使用全基因组DNA甲基化的高通量定量分析,即Illumina GoldenGate BeadArray,分析了来自多个个体的多个组织的DNA甲基化模式。 DNA甲基化模式在11个不同组织(r = 0.852)和六个个体(r = 0.829)中基本保持保守,我们发现DNA在非CpG岛和/或未被H3K4me3占据的CpG位点中高度甲基化或H3K27me3(P <0.05)。最终,我们发现Illumina GoldenGate检测具有大量包含单核苷酸多态性的探针(265/1505探针,占17.6%),这可能会干扰全基因组研究中的DNA甲基化分析。

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