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鉴定一个新的位点,并验证先前报道的与吸烟相关的差异甲基化的位点。REGICOR 研究。

Identification of a new locus and validation of previously reported loci showing differential methylation associated with smoking. The REGICOR study.

机构信息

a Cardiovascular Epidemiology and Genetics Research Group; IMIM (Hospital del Mar Medical Research Institute); 08003 Barcelona , Catalonia , Spain.

b Universitat Pompeu Fabra (UPF); 08003 Barcelona , Catalonia , Spain.

出版信息

Epigenetics. 2015;10(12):1156-65. doi: 10.1080/15592294.2015.1115175.

Abstract

Smoking increases the risk of many diseases and could act through changes in DNA methylation patterns. The aims of this study were to determine the association between smoking and DNA methylation throughout the genome at cytosine-phosphate-guanine (CpG) site level and genomic regions. A discovery cross-sectional epigenome-wide association study nested in the follow-up of the REGICOR cohort was designed and included 645 individuals. Blood DNA methylation was assessed using the Illumina HumanMethylation450 BeadChip. Smoking status was self-reported using a standardized questionnaire. We identified 66 differentially methylated CpG sites associated with smoking, located in 38 genes. In most of these CpG sites, we observed a trend among those quitting smoking to recover methylation levels typical of never smokers. A CpG site located in a novel smoking-associated gene (cg06394460 in LNX2) was hypomethylated in current smokers. Moreover, we validated two previously reported CpG sites (cg05886626 in THBS1, and cg24838345 in MTSS1) for their potential relation to atherosclerosis and cancer diseases, using several different approaches: CpG site methylation, gene expression, and plasma protein level determinations. Smoking was also associated with higher THBS1 gene expression but with lower levels of thrombospondin-1 in plasma. Finally, we identified differential methylation regions in 13 genes and in four non-coding RNAs. In summary, this study replicated previous findings and identified and validated a new CpG site located in LNX2 associated with smoking.

摘要

吸烟会增加许多疾病的风险,并且可能通过改变 DNA 甲基化模式来发挥作用。本研究的目的是确定吸烟与整个基因组在胞嘧啶-磷酸-鸟嘌呤(CpG)位点水平和基因组区域的 DNA 甲基化之间的关联。一项在 REGICOR 队列随访中嵌套的发现性横断面全基因组表观遗传关联研究被设计出来,并纳入了 645 名个体。使用 Illumina HumanMethylation450 BeadChip 评估血液 DNA 甲基化。使用标准化问卷自我报告吸烟状况。我们确定了 66 个与吸烟相关的差异甲基化 CpG 位点,位于 38 个基因中。在这些 CpG 位点中,我们观察到那些正在戒烟的人有恢复到从不吸烟者典型甲基化水平的趋势。一个位于新的与吸烟相关基因(LXN2 中的 cg06394460)中的 CpG 位点在当前吸烟者中呈低甲基化状态。此外,我们使用几种不同的方法验证了两个先前报道的与动脉粥样硬化和癌症疾病相关的 CpG 位点(THBS1 中的 cg05886626 和 MTSS1 中的 cg24838345)的潜在关系:CpG 位点甲基化、基因表达和血浆蛋白水平测定。吸烟还与 THBS1 基因表达升高但血浆中血栓素-1 水平降低有关。最后,我们确定了 13 个基因和 4 个非编码 RNA 中的差异甲基化区域。总之,本研究复制了先前的发现,并确定和验证了一个位于 LXN2 与吸烟相关的新 CpG 位点。

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