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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Germ-line mutations, DNA damage, and global hypermethylation in mice exposed to particulate air pollution in an urban/industrial location
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Germ-line mutations, DNA damage, and global hypermethylation in mice exposed to particulate air pollution in an urban/industrial location

机译:暴露于城市/工业场所空气中的颗粒物污染的小鼠中的种系突变,DNA损伤和总体甲基化过高

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Particulate air pollution is widespread, yet we have little understanding of the long-term health implications associated with exposure. We investigated DNA damage, mutation, and methylation in gametes of male mice exposed to particulate air pollution in an industrial/ urban environment. C57BL/CBA mice were exposed in situ to ambient air near two integrated steel mills and a major highway, alongside control mice breathing high-efficiency air particulate (HEPA) filtered ambient air. PCR analysis of an expanded simple tandem repeat (ESTR) locus revealed a 1.6-fold increase in sperm mutation frequency in mice exposed to ambient air for 10 wks, followed by a 6-wk break, compared with -HEPA-filtered air, indicating that mutations were induced in spermatogonial stem cells. DNA collected after 3 or 10 wks of exposure did not exhibit increased mutation frequency. Bulky DNA adducts were below the detection threshold in testes samples, suggesting that DNA reactive chemicals do not reach the germ line and cause ESTR mutation. In contrast, DNA strand breaks were elevated at 3 and 10 wks, possibly resulting from oxidative stress arising from exposure to particles and associated airborne pollutants. Sperm DNA was hypermethylated in mice breathing ambient relative to HEPA-filtered air and this change persisted following removal from the environmental exposure. Increased germ-line DNA mutation frequencies may cause population-level changes in genetic composition and disease. Changes in methylation can have widespread repercussions for chromatin structure, gene expression and genome stability. Potential health effects warrant extensive further investigation.
机译:空气污染十分普遍,但我们对与暴露有关的长期健康影响知之甚少。我们调查了在工业/城市环境中暴露于颗粒空气污染的雄性小鼠配子中的DNA损伤,突变和甲基化。将C57BL / CBA小鼠原位暴露于两家综合钢铁厂和一条主要高速公路附近的环境空气中,而对照小鼠则呼吸经高效空气颗粒(HEPA)过滤的环境空气。对扩展的简单串联重复(ESTR)基因座进行的PCR分析显示,与-HEPA过滤的空气相比,暴露于环境空气10周的小鼠的精子突变频率增加了1.6倍,随后发生了6周的中断,这表明在精原干细胞中诱导了突变。暴露3或10周后收集的DNA没有显示出增加的突变频率。睾丸样本中的大体积DNA加合物低于检测阈值,表明DNA反应性化学物质未到达种系并引起ESTR突变。相反,DNA链断裂在3和10 wks时升高,可能是由于暴露于颗粒和相关的空气传播污染物而产生的氧化应激所致。相对于经HEPA过滤的空气,在呼吸环境的小鼠中,精子DNA甲基化程度很高,这种变化在从环境暴露中去除后仍然持续存在。种系DNA突变频率增加可能会导致种群水平的遗传组成和疾病发生变化。甲基化的变化会对染色质结构,基因表达和基因组稳定性产生广泛影响。潜在的健康影响值得进一步研究。

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