The Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, United Kingdom.
Genome Res. 2012 Nov;22(11):2138-45. doi: 10.1101/gr.134304.111. Epub 2012 Aug 23.
A major concern in common disease epigenomics is distinguishing causal from consequential epigenetic variation. One means of addressing this issue is to identify the temporal origins of epigenetic variants via longitudinal analyses. However, prospective birth-cohort studies are expensive and time consuming. Here, we report DNA methylomics of archived Guthrie cards for the retrospective longitudinal analyses of in-utero-derived DNA methylation variation. We first validate two methodologies for generating comprehensive DNA methylomes from Guthrie cards. Then, using an integrated epigenomic/genomic analysis of Guthrie cards and follow-up samplings, we identify interindividual DNA methylation variation that is present both at birth and 3 yr later. These findings suggest that disease-relevant epigenetic variation could be detected at birth, i.e., before overt clinical disease. Guthrie card methylomics offers a potentially powerful and cost-effective strategy for studying the dynamics of interindividual epigenomic variation in a range of common human diseases.
常见疾病表观基因组学的一个主要关注点是区分因果性和继发性表观遗传变异。解决这个问题的一种方法是通过纵向分析来确定表观变异的时间起源。然而,前瞻性的出生队列研究既昂贵又耗时。在这里,我们报告了 Guthrie 卡的 DNA 甲基组学,以对胎儿来源的 DNA 甲基化变异进行回顾性纵向分析。我们首先验证了两种从 Guthrie 卡生成全面 DNA 甲基组的方法。然后,通过对 Guthrie 卡和后续采样的综合表观基因组/基因组分析,我们鉴定了在出生时和 3 年后都存在的个体间 DNA 甲基化变异。这些发现表明,与疾病相关的表观遗传变异可能在出生时,即在明显的临床疾病之前就可以被检测到。Guthrie 卡甲基组学为研究一系列常见人类疾病中个体间表观基因组变异的动态提供了一种潜在的强大且具有成本效益的策略。