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首页> 外文期刊>Epigenetics & Chromatin >Genome-wide analysis of DNA methylation in buccal cells: a study of monozygotic twins and mQTLs
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Genome-wide analysis of DNA methylation in buccal cells: a study of monozygotic twins and mQTLs

机译:全基因组分析颊细胞DNA甲基化:单卵双胞胎和mQTLs的研究。

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DNA methylation arrays are widely used in epigenome-wide association studies and methylation quantitative trait locus (mQTL) studies. Here, we performed the first genome-wide analysis of monozygotic (MZ) twin correlations and mQTLs on data obtained with the Illumina MethylationEPIC BeadChip (EPIC array) and compared the performance of the EPIC array to the Illumina HumanMethylation450 BeadChip (HM450 array) for buccal-derived DNA. Good-quality EPIC data were obtained for 102 buccal-derived DNA samples from 49 MZ twin pairs (mean age?=?7.5?years, range?=?1–10). Differences between MZ twins in the cellular content of buccal swabs were a major driver for differences in their DNA methylation profiles, highlighting the importance to adjust for cellular composition in DNA methylation studies of buccal-derived DNA. After adjusting for cellular composition, the genome-wide mean correlation (r) between MZ twins was 0.21 for the EPIC array, and cis mQTL analysis in 84 twins identified 1,296,323 significant associations (FDR 5%), encompassing 33,749 methylation sites and 616,029 genetic variants. MZ twin correlations were slightly larger (p??2.2?×?10?16) for novel EPIC probes (N?=?383,066, mean r?=?0.22) compared to probes that are also present on HM450 (N?=?406,822, mean r?=?0.20). In line with this observation, a larger percentage of novel EPIC probes was associated with genetic variants (novel EPIC probes with significant mQTL 4.7%, HM450 probes with mQTL 3.9%, p??2.2?×?10?16). Methylation sites with a large MZ correlation and sites associated with mQTLs were most strongly enriched in epithelial cell DNase I hypersensitive sites (DHSs), enhancers, and histone mark H3K4me3. We conclude that the contribution of familial factors to individual differences in DNA methylation and the effect of mQTLs are larger for novel EPIC probes, especially those within regulatory elements connected to active regions specific to the investigated tissue.
机译:DNA甲基化阵列广泛用于表观基因组范围的关联研究和甲基化定量性状基因座(mQTL)研究中。在这里,我们对通过Illumina甲基化EPIC BeadChip(EPIC阵列)获得的数据进行了单合子(MZ)孪生相关性和mQTL的首次全基因组分析,并将EPIC阵列与Illumina HumanMethylation450 BeadChip(HM450阵列)的性能进行了比较。衍生的DNA。从49对MZ双胞胎中获得102份颊颊来源的DNA样品的高质量EPIC数据(平均年龄== 7.5年,范围范围= 1-10)。口腔拭子细胞含量中MZ双胞胎之间的差异是其DNA甲基化谱图差异的主要驱动力,突显了在颊源DNA的DNA甲基化研究中调整细胞组成的重要性。调整细胞组成后,EPIC阵列的MZ双胞胎之间的全基因组平均关联度(r)为0.21,对84个双胞胎的顺式mQTL分析确定了1,296,323个重要关联(FDR 5%),包括33,749个甲基化位点和616,029个遗传变异。与同样存在于HM450上的探针(N ==)相比,新型EPIC探针的MZ孪生相关性稍大(p?<?2.2?×?10?16)(N?=?383,066,平均r?=?0.22)。 ≤406822,平均值r≤0.20)。与该观察结果一致,更大百分比的新型EPIC探针与遗传变异相关(具有显着的mQTL 4.7%的新的EPIC探针,具有mQTL的3.9%的HM450探针,p≤<2.2≤×≤10≤16)。具有较大MZ相关性的甲基化位点和与mQTL相关的位点在上皮细胞DNase I超敏位点(DHS),增强子和组蛋白标记H3K4me3中最丰富。我们得出结论,对于新型EPIC探针,家族因子对DNA甲基化个体差异的贡献和mQTL的影响更大,尤其是那些与特定于研究组织的活性区域相连的调节元件内的探针。

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