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吸烟会导致 DNA 甲基化的广泛全基因组改变。

Tobacco smoking leads to extensive genome-wide changes in DNA methylation.

机构信息

Research Unit of Molecular Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

出版信息

PLoS One. 2013 May 17;8(5):e63812. doi: 10.1371/journal.pone.0063812. Print 2013.

DOI:10.1371/journal.pone.0063812
PMID:23691101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3656907/
Abstract

Environmental factors such as tobacco smoking may have long-lasting effects on DNA methylation patterns, which might lead to changes in gene expression and in a broader context to the development or progression of various diseases. We conducted an epigenome-wide association study (EWAs) comparing current, former and never smokers from 1793 participants of the population-based KORA F4 panel, with replication in 479 participants from the KORA F3 panel, carried out by the 450K BeadChip with genomic DNA obtained from whole blood. We observed wide-spread differences in the degree of site-specific methylation (with p-values ranging from 9.31E-08 to 2.54E-182) as a function of tobacco smoking in each of the 22 autosomes, with the percent of variance explained by smoking ranging from 1.31 to 41.02. Depending on cessation time and pack-years, methylation levels in former smokers were found to be close to the ones seen in never smokers. In addition, methylation-specific protein binding patterns were observed for cg05575921 within AHRR, which had the highest level of detectable changes in DNA methylation associated with tobacco smoking (-24.40% methylation; p = 2.54E-182), suggesting a regulatory role for gene expression. The results of our study confirm the broad effect of tobacco smoking on the human organism, but also show that quitting tobacco smoking presumably allows regaining the DNA methylation state of never smokers.

摘要

环境因素,如吸烟,可能对 DNA 甲基化模式产生持久影响,这可能导致基因表达的变化,并在更广泛的范围内导致各种疾病的发生或进展。我们进行了一项基于人群的 KORA F4 面板中 1793 名参与者的当前、曾经和从不吸烟者的全基因组关联研究(EWAS),并在基于全血基因组 DNA 的 450K BeadChip 上进行了复制,共有来自 KORA F3 面板的 479 名参与者参与。我们观察到,在 22 条常染色体上,吸烟与特定部位的甲基化程度存在广泛差异(p 值范围从 9.31E-08 到 2.54E-182),吸烟解释的变异百分比范围从 1.31 到 41.02。根据戒烟时间和吸烟年数,发现曾经吸烟者的甲基化水平接近从不吸烟者。此外,在 AHRR 内的 cg05575921 观察到了甲基化特异性蛋白结合模式,该模式与吸烟相关的 DNA 甲基化变化程度最高(-24.40%的甲基化;p = 2.54E-182),表明其对基因表达具有调节作用。我们的研究结果证实了吸烟对人体的广泛影响,但也表明戒烟可能允许恢复从不吸烟者的 DNA 甲基化状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41c/3656907/12ac2f15c07b/pone.0063812.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41c/3656907/ca2fdad99f12/pone.0063812.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41c/3656907/12ac2f15c07b/pone.0063812.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41c/3656907/ca2fdad99f12/pone.0063812.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41c/3656907/12ac2f15c07b/pone.0063812.g002.jpg

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