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妊娠砷暴露与父系跨代表观遗传遗传。

Gestational arsenic exposure and paternal intergenerational epigenetic inheritance.

机构信息

Center for Health and Environmental Risk Research, National Institute for Environmental Studies, Tsukuba 305-8506, Japan.

Center for Health and Environmental Risk Research, National Institute for Environmental Studies, Tsukuba 305-8506, Japan.

出版信息

Toxicol Appl Pharmacol. 2020 Dec 15;409:115319. doi: 10.1016/j.taap.2020.115319. Epub 2020 Nov 6.

DOI:10.1016/j.taap.2020.115319
PMID:33160984
Abstract

A growing body of evidence has shown that gestational exposure to environmental factors such as imbalanced diet, environmental chemicals, and stress can lead to late-onset health effects in offspring and that some of these effects are heritable by the next generation and subsequent generations. Furthermore, altered epigenetic modifications in DNA methylation, histone modifications and small RNAs in a single sperm genome have been shown to transmit disease phenotypes acquired from the environment to later generations. Recently, our group found that gestational exposure of F0 pregnant dams to an inorganic arsenic, sodium arsenite, increases the incidence of hepatic tumors in male F2 mice, and the effects are paternally transmitted to the F2. Here, we first overview the epigenetic changes involved in paternal intergenerational and transgenerational inheritance caused by exposure to environmental factors. Then, we discuss our recent studies regarding paternal inheritance of the tumor-augmenting effects in F2 mice by gestational arsenite exposure, in which we investigated alterations of DNA methylation status in F2 tumors and causative F1 sperm. We also discuss the possible targets of the F2 effects. Finally, we discuss future perspectives on the studies that are needed to fully understand the health effects of arsenic exposure.

摘要

越来越多的证据表明,胎儿在母体中暴露于饮食不均衡、环境化学物质和压力等环境因素会导致后代出现迟发性健康影响,其中一些影响可通过下一代和随后的几代遗传。此外,研究表明,单个精子基因组中的 DNA 甲基化、组蛋白修饰和小 RNA 的表观遗传修饰改变,可将从环境中获得的疾病表型传递给后代。最近,我们的研究小组发现,母体在妊娠期接触无机砷(亚砷酸钠)会增加雄性 F2 代小鼠肝脏肿瘤的发生率,并且这种影响是通过父系遗传给 F2 代的。在这里,我们首先概述了环境因素暴露引起的父代跨代和传递性遗传中的表观遗传变化。然后,我们讨论了我们最近关于母体妊娠期接触亚砷酸盐导致 F2 代小鼠肿瘤增强效应的父系遗传的研究,其中我们研究了 F2 代肿瘤和致病因 F1 精子中 DNA 甲基化状态的改变。我们还讨论了 F2 代效应的可能靶标。最后,我们讨论了未来需要进行哪些研究才能全面了解砷暴露的健康影响。

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Gestational arsenic exposure and paternal intergenerational epigenetic inheritance.妊娠砷暴露与父系跨代表观遗传遗传。
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