Ge Zhao-Jia, Luo Shi-Ming, Lin Fei, Liang Qiu-Xia, Huang Lin, Wei Yan-Chang, Hou Yi, Han Zhi-Ming, Schatten Heide, Sun Qing-Yuan
State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China.
Environ Health Perspect. 2014 Feb;122(2):159-64. doi: 10.1289/ehp.1307047. Epub 2013 Dec 6.
Maternal obesity has adverse effects on oocyte quality, embryo development, and the health of the offspring.
To understand the underlying mechanisms responsible for the negative effects of maternal obesity, we investigated the DNA methylation status of several imprinted genes and metabolism-related genes.
Using a high-fat-diet (HFD)-induced mouse model of obesity, we analyzed the DNA methylation of several imprinted genes and metabolism-related genes in oocytes from control and obese dams and in oocytes and liver from their offspring. Analysis was performed using combined bisulfite restriction analysis (COBRA) and bisulfite sequencing.
DNA methylation of imprinted genes in oocytes was not altered in either obese dams or their offspring; however, DNA methylation of metabolism-related genes was changed. In oocytes of obese mice, the DNA methylation level of the leptin (Lep) promoter was significantly increased and that of the Ppar-α promoter was reduced. Increased methylation of Lep and decreased methylation of Ppar-α was also observed in the liver of female offspring from dams fed the high-fat diet (OHFD). mRNA expression of Lep and Ppar-α was also significantly altered in the liver of these OHFD. In OHFD oocytes, the DNA methylation level of Ppar-α promoter was increased.
Our results indicate that DNA methylation patterns of several metabolism-related genes are changed not only in oocytes of obese mice but also in oocytes and liver of their offspring. These data may contribute to the understanding of adverse effects of maternal obesity on reproduction and health of the offspring.
母体肥胖对卵母细胞质量、胚胎发育及后代健康具有不利影响。
为了解母体肥胖产生负面影响的潜在机制,我们研究了多个印记基因和代谢相关基因的DNA甲基化状态。
利用高脂饮食(HFD)诱导的肥胖小鼠模型,我们分析了对照母鼠和肥胖母鼠的卵母细胞以及它们后代的卵母细胞和肝脏中多个印记基因和代谢相关基因的DNA甲基化情况。采用亚硫酸氢盐联合限制性分析(COBRA)和亚硫酸氢盐测序进行分析。
肥胖母鼠及其后代的卵母细胞中印记基因的DNA甲基化未发生改变;然而,代谢相关基因的DNA甲基化发生了变化。在肥胖小鼠的卵母细胞中,瘦素(Lep)启动子的DNA甲基化水平显著升高,而过氧化物酶体增殖物激活受体α(Ppar-α)启动子的DNA甲基化水平降低。在高脂饮食喂养的母鼠(OHFD)后代的雌性肝脏中也观察到Lep甲基化增加和Ppar-α甲基化减少。这些OHFD小鼠肝脏中Lep和Ppar-α的mRNA表达也显著改变。在OHFD卵母细胞中,Ppar-α启动子的DNA甲基化水平升高。
我们的结果表明,多个代谢相关基因的DNA甲基化模式不仅在肥胖小鼠的卵母细胞中发生改变,在其后代的卵母细胞和肝脏中也发生改变。这些数据可能有助于理解母体肥胖对后代生殖和健康的不利影响。