首页> 外文期刊>Toxicology and Applied Pharmacology >Developmental exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin alters DNA methyltransferase (dnmt) expression in zebrafish (Danio rerio)
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Developmental exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin alters DNA methyltransferase (dnmt) expression in zebrafish (Danio rerio)

机译:发育中的2,3,7,8-四氯二苯并-对-二恶英暴露会改变斑马鱼(Danio rerio)中的DNA甲基转移酶(dnmt)表达

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摘要

DNA methylation is one of the most important epigenetic modifications involved in the regulation of gene expression. The DNA methylation reaction is catalyzed by DNA methyltransferases (DNMTs). Recent studies have demonstrated that toxicants can affect normal development by altering DNA methylation patterns, but the mechanisms of action are poorly understood. Hence, we tested the hypothesis that developmental exposure to TCDD affects dnmt gene expression patterns. Zebrafish embryos were exposed to 5 nM TCDD for 1 h from 4 to 5 h post-fertilization (hpf) and sampled at 12, 24, 48, 72, and 96 hpf to determine dnmt gene expression and DNA methylation patterns. We performed a detailed analysis of zebrafish dnmt gene expression during development and in adult tissues. Our results demonstrate that dnmt3b genes are highly expressed in early stages of development, and dnmt3a genes are more abundant in later stages. TCDD exposure upregulated dnmt1 and dnmt3b2 expression, whereas dnmt3a1, 3b1, and 3b4 are downregulated following exposure. We did not observe any TCDD-induced differences in global methylation or hydroxymethylation levels, but the promoter methylation of aryl hydrocarbon receptor (AHR) target genes was altered. In TCDD-exposed embryos, AHR repressor a (ahrra) and c-fos promoters were differentially methylated. To characterize the TCDD effects on DNMTs, we cloned the dnmt promoters with xenobiotic response elements and conducted AHR transactivation assays using a luciferase reporter system. Our results suggest that ahr2 can regulate dnmt3a1, dnmt3a2, and dnmt3b2 expression. Overall, we demonstrate that developmental exposure to TCDD alters dnmt expression and DNA methylation patterns. (C) 2015 Elsevier Inc. All rights reserved.
机译:DNA甲基化是参与基因表达调控的最重要的表观遗传修饰之一。 DNA甲基化反应由DNA甲基转移酶(DNMT)催化。最近的研究表明,有毒物质可通过改变DNA甲基化模式来影响正常发育,但其作用机理尚不清楚。因此,我们测试了TCDD发育暴露影响dnmt基因表达模式的假说。从受精后(hpf)4至5 h,将斑马鱼胚胎暴露于5 nM TCDD 1 h,并在12、24、48、72和96 hpf采样,以确定dnmt基因表达和DNA甲基化模式。我们对发育过程中和成年组织中的斑马鱼dnmt基因表达进行了详细的分析。我们的结果表明dnmt3b基因在发育的早期阶段高表达,而dnmt3a基因在后期的阶段更为丰富。 TCDD暴露上调dnmt1和dnmt3b2表达,而dnmt3a1、3b1和3b4在暴露后下调。我们没有观察到任何TCDD诱导的总体甲基化或羟甲基化水平的差异,但是芳烃受体(AHR)目标基因的启动子甲基化发生了改变。在暴露于TCDD的胚胎中,AHR阻遏物a(ahrra)和c-fos启动子被差异甲基化。为了表征TCDD对DNMT的作用,我们克隆了具有异源生物反应元件的dnmt启动子,并使用荧光素酶报告系统进行了AHR反式激活分析。我们的结果表明ahr2可以调节dnmt3a1,dnmt3a2和dnmt3b2的表达。总的来说,我们证明了TCDD的发育暴露会改变dnmt表达和DNA甲基化模式。 (C)2015 Elsevier Inc.保留所有权利。

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