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Neural Tube Defects and ZIC4 Hypomethylation in Relation to Polycyclic Aromatic Hydrocarbon Exposure

机译:多环芳烃暴露的神经管缺陷和ZIC4低甲基化

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Background: Epigenetic dysregulation is one of the postulated underlying mechanisms of neural tube defects (NTDs). Polycyclic aromatic hydrocarbons (PAHs), a group of environmental pollutants that are reported as a risk factor of NTDs, may cause decreased genome-wide DNA methylation. With DNA extracted from neural tissues, this study identified gene(s) whose hypomethylation was related to elevated risk for NTDs and examined whether its hypomethylation is related to PAH exposure. Results: Using data profiled by Infinium HumanMethylation450 BeadChip array from 10 NTD cases and 8 controls, ZIC4, CASP8, RAB32, RARA, and TRAF6 were identified to be the top 5 genes in NTD-related hypomethylated gene families. Among all identified genes, ZIC4 had the largest number of differently methylated CpG sites (n = 13) in the promoter and 5'UTR. Significantly decreased methylation in ZIC4 promoter and 5'UTR was verified in an independent cohort of 80 cases and 32 controls (p 0.001) utilizing the Sequenom EpiTYPER platform. Hypomethylation of ZIC4 was associated with a higher risk of NTDs (adjusted OR = 1.08; 95% CI: 1.03, 1.13) in a logistic regression model. Mean methylation levels in the promoter and 5'UTR region of ZIC4 tended to be inversely associated with levels of high-molecular-weight PAHs in fetal liver among NTD fetuses (β [95% CI]: - 0.045 [-0.091, 0.001], p = 0.054). Six and three CpG sites in ZIC4 promoter and 5'UTR were inversely correlated with antioxidant indicators and protein oxidation markers (ρ: -0.45 to -0.75, p 0.05) in fetal neural tissues, respectively. In a whole-embryo cultured mouse model, hypomethylation of Zic4 promoter and 5'UTR, and upregulation of Zic4 were observed, coupled with increased NTD rates after BaP exposure. The antioxidant N-acetyl-L-cysteine normalized the changes observed in the BaP exposure group. Conclusions: Hypomethylation of ZIC4 promoter and 5'UTR may increase the risk for NTDs; oxidative stress is likely to play a role in the methylation change of Zic4 in response to PAH exposure in NTD formation.
机译:背景:表观遗传失调是神经管缺陷(NTDS)的假设潜在机制之一。多环芳烃(PAHS),作为NTDS危险因子报告的一组环境污染物,可能导致基因组宽的DNA甲基化。通过从神经组织中提取的DNA,该研究鉴定了低甲基化与NTDS的升高风险有关的基因,并检查其低甲基化与PAH暴露有关。结果:使用来自10个NTD病例和8个对照,ZIC4,CasP8,RAB32,RARA和TRAF6的数据分解的数据分析了450珠芯片阵列,鉴定为与NTD相关的低甲基化基因家族中的前5个基因。在所有鉴定的基因中,ZIC4在启动子和5'UTR中具有最大数量的不同甲基化CPG位点(n = 13)。在ZiC4启动子中显着降低甲基化,在80例的独立队列和32例对照(P <0.001)中验证了5'UTR。在逻辑回归模型中,ZiC4的低​​甲基化与NTDS的风险较高(调节或= 1.08; 95%CI:1.03,1.13)。 ZIC4的促进剂和5'UTR区域中的平均甲基化水平往返NTD胎儿中胎儿肝中的高分子重量PAH水平(β[95%CI]: - 0.045 [-0.091,0001], p = 0.054)。 ZIC4启动子和5'UTR中的六个和三个CPG位点分别与胎儿神经组织中的抗氧化剂指示剂和蛋白氧化标志物(ρ:-0.45至-0.75,P <0.05)相关。在全胚胎培养的小鼠模型中,观察到ZIC4启动子和5'UTR的低甲基化,ZIC4的上调,偶联在BAP暴露后增加的NTD速率。抗氧化N-乙酰基-1-半胱氨酸标准化在烘烤曝光组中观察到的变化。结论:ZIC4启动子和5'UTR的低甲基化可能会增加NTD的风险;氧化应激可能在抗NTD形成中的PAH暴露时在ZIC4的甲基化变化中发挥作用。

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