Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS Genet. 2010 May 13;6(5):e1000952. doi: 10.1371/journal.pgen.1000952.
A fundamental challenge in the post-genome era is to understand and annotate the consequences of genetic variation, particularly within the context of human tissues. We present a set of integrated experiments that investigate the effects of common genetic variability on DNA methylation and mRNA expression in four human brain regions each from 150 individuals (600 samples total). We find an abundance of genetic cis regulation of mRNA expression and show for the first time abundant quantitative trait loci for DNA CpG methylation across the genome. We show peak enrichment for cis expression QTLs to be approximately 68,000 bp away from individual transcription start sites; however, the peak enrichment for cis CpG methylation QTLs is located much closer, only 45 bp from the CpG site in question. We observe that the largest magnitude quantitative trait loci occur across distinct brain tissues. Our analyses reveal that CpG methylation quantitative trait loci are more likely to occur for CpG sites outside of islands. Lastly, we show that while we can observe individual QTLs that appear to affect both the level of a transcript and a physically close CpG methylation site, these are quite rare. We believe these data, which we have made publicly available, will provide a critical step toward understanding the biological effects of genetic variation.
在后基因组时代,一个基本的挑战是理解和注释遗传变异的后果,特别是在人类组织的背景下。我们提出了一系列综合实验,研究了常见遗传变异对四个人类大脑区域中每个区域的 150 个人(总共 600 个样本)的 DNA 甲基化和 mRNA 表达的影响。我们发现大量的 mRNA 表达的顺式调控遗传,并首次显示出大量的全基因组 DNA CpG 甲基化的数量性状基因座。我们发现顺式表达 QTL 的峰富集距离单个转录起始位点约 68000bp;然而,顺式 CpG 甲基化 QTL 的峰富集位置要近得多,仅距离所研究的 CpG 位点 45bp。我们观察到最大幅度的数量性状基因座发生在不同的脑组织中。我们的分析表明,CpG 甲基化数量性状基因座更可能发生在岛外的 CpG 位点。最后,我们表明,虽然我们可以观察到似乎同时影响转录本水平和物理上接近的 CpG 甲基化位点的单个 QTL,但这种情况相当罕见。我们相信,我们公开提供的这些数据将为理解遗传变异的生物学效应提供一个关键步骤。