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父代苯并[a]芘暴露可改变 F0 代小鼠精子印迹基因的 DNA 甲基化水平及其未暴露的 F1-2 雄性后代。

Paternal benzo[a]pyrene exposure alters the sperm DNA methylation levels of imprinting genes in F0 generation mice and their unexposed F1-2 male offspring.

机构信息

Department of Toxicology, School of Public Health, Shanxi Medical University, Shanxi, Taiyuan 030001, China.

Department of Children and Adolescences Health, School of Public Health, Shanxi Medical University, Shanxi, Taiyuan 030001, China.

出版信息

Chemosphere. 2019 Aug;228:586-594. doi: 10.1016/j.chemosphere.2019.04.092. Epub 2019 Apr 28.

Abstract

BACKGROUND

Benzo[a]pyrene (BaP) is an environmental pollutant known to cause teratogenesis. However, the mechanism underlying this teratogenic effect is not fully understood. Recently, the alteration of DNA methylation of imprinting genes has emerged as a specific epigenetic mechanism linking the impact of environmental pollutants on embryonic development to paternal exposures. The aim of this study was to investigate the transgenerational effects of paternal BaP exposure on the imprinting genes in mouse sperm DNA.

METHODS

Male C57BL/6J mice received BaP (1.0 or 2.5 mg/kg) or olive oil twice a week for 12 weeks. The methylation status of 6 imprinting genes (H19, Meg3, Peg1, Peg3, Igf2 and Snrpn) was examined by bisulfite pyrosequencing of the sperm DNA of BaP-exposed F0 generation and their offspring.

RESULTS

BaP exposure reduced the methylation levels in the imprinting genes H19 and Meg3 and increased the methylation levels of Peg1 and Peg3; however, no significant differences was observed for the methylation levels of Igf2 or Snrpn in the sperm DNA. Furthermore, BaP-exposed male mice were mated with unexposed female mice to generate F1-2 generations. The methylation levels of the 6 genes in the sperm DNA from F1-2 offspring showed a similar pattern as that of the F0 male. The effects were attenuated in F1-2 generations.

CONCLUSIONS

Paternal BaP exposure altered the methylation levels of imprinting genes, implicating that imprinting genes are susceptible to environmental toxicants. Furthermore, a similar alteration was observed in the F1-2 generations although the attenuated in methylation in F2 generation, revealing a potential transgenerational effect.

摘要

背景

苯并[a]芘(BaP)是一种环境污染物,已知会导致致畸。然而,这种致畸作用的机制尚未完全阐明。最近,印迹基因的 DNA 甲基化改变已成为将环境污染物对胚胎发育的影响与父代暴露联系起来的特定表观遗传机制。本研究旨在探讨父代 BaP 暴露对小鼠精子 DNA 印迹基因的跨代效应。

方法

雄性 C57BL/6J 小鼠每周接受 BaP(1.0 或 2.5mg/kg)或橄榄油两次,共 12 周。通过对 BaP 暴露的 F0 代及其后代精子 DNA 的亚硫酸氢盐焦磷酸测序,检测 6 个印迹基因(H19、Meg3、Peg1、Peg3、Igf2 和 Snrpn)的甲基化状态。

结果

BaP 暴露降低了印迹基因 H19 和 Meg3 的甲基化水平,增加了 Peg1 和 Peg3 的甲基化水平;然而,精子 DNA 中 Igf2 或 Snrpn 的甲基化水平没有显著差异。此外,BaP 暴露的雄性小鼠与未暴露的雌性小鼠交配,产生 F1-2 代。F1-2 代后代精子 DNA 中 6 个基因的甲基化水平呈现出与 F0 雄性相似的模式。这种效应在 F1-2 代中减弱。

结论

父代 BaP 暴露改变了印迹基因的甲基化水平,表明印迹基因易受环境毒物的影响。此外,尽管在 F2 代中甲基化减弱,但在 F1-2 代中观察到类似的改变,揭示了潜在的跨代效应。

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