Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT, USA.
Department of Psychology, University of Utah, Salt Lake City, UT, USA.
Andrology. 2017 Nov;5(6):1089-1099. doi: 10.1111/andr.12416. Epub 2017 Sep 26.
Numerous health consequences of tobacco smoke exposure have been characterized, and the effects of smoking on traditional measures of male fertility are well described. However, a growing body of data indicates that pre-conception paternal smoking also confers increased risk for a number of morbidities on offspring. The mechanism for this increased risk has not been elucidated, but it is likely mediated, at least in part, through epigenetic modifications transmitted through spermatozoa. In this study, we investigated the impact of cigarette smoke exposure on sperm DNA methylation patterns in 78 men who smoke and 78 never-smokers using the Infinium Human Methylation 450 beadchip. We investigated two models of DNA methylation alterations: (i) consistently altered methylation at specific CpGs or within specific genomic regions and (ii) stochastic DNA methylation alterations manifest as increased variability in genome-wide methylation patterns in men who smoke. We identified 141 significantly differentially methylated CpGs associated with smoking. In addition, we identified a trend toward increased variance in methylation patterns genome-wide in sperm DNA from men who smoke compared with never-smokers. These findings of widespread DNA methylation alterations are consistent with the broad range of offspring heath disparities associated with pre-conception paternal smoke exposure and warrant further investigation to identify the specific mechanism by which sperm DNA methylation perturbation confers risk to offspring health and whether these changes can be transmitted to offspring and transgenerationally.
已经描述了暴露于烟草烟雾的许多健康后果,并且吸烟对传统男性生育力衡量标准的影响也得到了很好的描述。然而,越来越多的数据表明,孕前父亲吸烟也会增加后代多种疾病的风险。这种风险增加的机制尚未阐明,但很可能至少部分通过通过精子传递的表观遗传修饰来介导。在这项研究中,我们使用 Infinium Human Methylation 450 珠芯片调查了 78 名吸烟男性和 78 名不吸烟男性的精子 DNA 甲基化模式受香烟烟雾暴露的影响。我们研究了两种 DNA 甲基化改变模型:(i)在特定 CpG 或特定基因组区域中一致改变的甲基化,和(ii)随机的 DNA 甲基化改变表现为吸烟男性全基因组甲基化模式中增加的可变性。我们鉴定出 141 个与吸烟相关的显着差异甲基化 CpG。此外,我们发现与从不吸烟者相比,吸烟男性精子 DNA 中全基因组的甲基化模式的方差呈增加趋势。这些广泛的 DNA 甲基化改变的发现与与孕前父亲吸烟有关的广泛的后代健康差异一致,值得进一步研究以确定精子 DNA 甲基化扰动通过何种具体机制赋予后代健康风险,以及这些变化是否可以传递给后代和跨代。