Huang Yun, Lin Shanshan, Wang Chengrong, Pi Xin, Jin Lei, Li Zhiwen, Wang Linlin, Ren Aiguo
National Health Commission Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, Institute of Reproductive and Child Health, School of Public Health, Peking University Health Science Center, Beijing, China.
Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Front Cell Dev Biol. 2020 Nov 16;8:582661. doi: 10.3389/fcell.2020.582661. eCollection 2020.
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.
Using data profiled by Infinium HumanMethylation450 BeadChip array from 10 NTD cases and eight controls, , , , , and were identified to be the top five genes in NTD-related hypomethylated gene families. Among all identified genes, had the largest number of differently methylated CpG sites ( = 13) in the promoter region and 5' UTR. Significantly decreased methylation in the promoter region and 5' UTR was verified in an independent cohort of 80 cases and 32 controls ( < 0.001) utilizing the Sequenom EpiTYPER platform. Hypomethylation of was associated with a higher risk of NTDs [adjusted OR = 1.08; 95% confidence interval (CI): 1.03, 1.13] in a logistic regression model. Mean methylation levels in the promoter region and 5' UTR of 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], = 0.054). Six and three CpG sites in the promoter region and 5' UTR were inversely correlated with antioxidant indicators and protein oxidation markers (: -0.45 to -0.75, < 0.05) in fetal neural tissues, respectively. In a whole-embryo cultured mouse model, hypomethylation of the promoter region and 5' UTR and upregulation of were observed, coupled with increased NTD rates after BaP exposure. The antioxidant -acetyl-L-cysteine normalized the changes observed in the BaP exposure group.
Hypomethylation of the promoter region and 5' UTR may increase the risk for NTDs; oxidative stress is likely to play a role in the methylation change of in response to PAH exposure in NTD formation.
表观遗传失调是神经管缺陷(NTDs)潜在的发病机制之一。多环芳烃(PAHs)是一类环境污染物,被报道为NTDs的一个风险因素,可能导致全基因组DNA甲基化水平降低。本研究利用从神经组织中提取的DNA,鉴定出甲基化水平降低与NTDs风险升高相关的基因,并检测其甲基化水平降低是否与PAH暴露有关。
利用来自10例NTD病例和8例对照的Infinium HumanMethylation450 BeadChip芯片数据,鉴定出 、 、 、 和 是NTD相关低甲基化基因家族中的前五个基因。在所有鉴定出的基因中, 在启动子区域和5'非翻译区(UTR)具有最多数量的差异甲基化CpG位点( = 13)。利用Sequenom EpiTYPER平台,在一个由80例病例和32例对照组成的独立队列中验证了 启动子区域和5' UTR的甲基化水平显著降低( < 0.001)。在逻辑回归模型中, 的低甲基化与NTDs的较高风险相关[调整后的比值比(OR) = 1.08;95%置信区间(CI):1.03,1.13]。在NTD胎儿中, 启动子区域和5' UTR的平均甲基化水平往往与胎儿肝脏中高分子量PAHs的水平呈负相关(β [95% CI]:-0.045 [-0.091,0.001], = 0.054)。在胎儿神经组织中, 启动子区域和5' UTR中的6个和3个CpG位点分别与抗氧化指标和蛋白质氧化标记物呈负相关(:-0.45至-0.75, < 0.05)。在全胚胎培养的小鼠模型中,观察到 启动子区域和5' UTR的低甲基化以及 的上调,同时在暴露于苯并[a]芘(BaP)后NTD发生率增加。抗氧化剂N-乙酰-L-半胱氨酸使BaP暴露组中观察到的变化恢复正常。
启动子区域和5' UTR的低甲基化可能增加NTDs的风险;氧化应激可能在NTD形成过程中PAH暴露导致的 的甲基化变化中起作用。