Department of Epidemiology, Rollins School of Public Health, Emory University, 1518 Clifton Road NE #3049, Atlanta, GA, 30322, USA.
Hum Genet. 2013 Sep;132(9):1027-37. doi: 10.1007/s00439-013-1311-6. Epub 2013 May 9.
Cigarette smoking is an environmental risk factor for many chronic diseases, and disease risk can often be managed by smoking control. Smoking can induce cellular and molecular changes, including epigenetic modification, but the short- and long-term epigenetic modifications caused by cigarette smoking at the gene level have not been well understood. Recent studies have identified smoking-related DNA methylation (DNAm) sites in Caucasians. To determine whether the same DNAm sites associate with smoking in African Americans, and to identify novel smoking-related DNAm sites, we conducted a methylome-wide association study of cigarette smoking using a discovery sample of 972 African Americans, and a replication sample of 239 African Americans with two array-based methods. Among 15 DNAm sites significantly associated with smoking after correction for multiple testing in our discovery sample, 5 DNAm sites are replicated in an independent cohort, and 14 sites in the replication sample have effects in the same direction as in the discovery sample. The top two smoking-related DNAm sites in F2RL3 (factor II receptor-like 3) and GPR15 (G-protein-coupled receptor 15) observed in African Americans are consistent with previous findings in Caucasians. The associations between the replicated DNAm sites and smoking remain significant after adjusting for genetic background. Despite the distinct genetic background between African Americans and Caucasians, the DNAm from the two ethnic groups shares common associations with cigarette smoking, which suggests a common molecular mechanism of epigenetic modification influenced by environmental exposure.
吸烟是许多慢性疾病的环境风险因素,疾病风险通常可以通过控烟来管理。吸烟可诱导细胞和分子变化,包括表观遗传修饰,但吸烟引起的短期和长期基因水平的表观遗传修饰尚未得到很好的理解。最近的研究已经在白种人中确定了与吸烟有关的 DNA 甲基化(DNAm)位点。为了确定在非裔美国人中是否存在与吸烟相关的相同 DNAm 位点,并确定新的与吸烟相关的 DNAm 位点,我们使用基于 972 名非裔美国人的发现样本和基于 239 名非裔美国人的两个基于阵列的方法的复制样本,进行了一项关于吸烟的全基因组甲基化关联研究。在我们的发现样本中,经过多次测试校正后,有 15 个 DNAm 位点与吸烟显著相关,其中 5 个 DNAm 位点在独立队列中得到复制,在复制样本中,有 14 个位点的效应与发现样本中的相同。在非裔美国人中观察到的 F2RL3(因子 II 受体样 3)和 GPR15(G 蛋白偶联受体 15)中与吸烟相关的两个最显著的 DNAm 位点与白种人之前的发现一致。在调整遗传背景后,复制的 DNAm 位点与吸烟之间的关联仍然显著。尽管非裔美国人和白种人之间存在明显的遗传背景差异,但这两个种族的 DNAm 与吸烟存在共同关联,这表明受环境暴露影响的表观遗传修饰存在共同的分子机制。