Cannon Matthew V, Buchner David A, Hester James, Miller Hadley, Sehayek Ephraim, Nadeau Joseph H, Serre David
Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
Department of Genetics, Case Western Reserve University, Cleveland, Ohio, United States of America.
PLoS One. 2014 Mar 3;9(3):e90335. doi: 10.1371/journal.pone.0090335. eCollection 2014.
Epidemiological and animal studies have shown that maternal diet can influence metabolism in adult offspring. However, the molecular mechanisms underlying these changes remain poorly understood. Here, we characterize the phenotypes induced by maternal obesity in a mouse model and examine gene expression and epigenetic changes induced by maternal diet in adult offspring.
We analyzed genetically identical male mice born from dams fed a high- or low-fat diet throughout pregnancy and until day 21 postpartum. After weaning, half of the males of each group were fed a high-fat diet, the other half a low-fat diet. We first characterized the genome-wide gene expression patterns of six tissues of adult offspring - liver, pancreas, white adipose, brain, muscle and heart. We then measured DNA methylation patterns in liver at selected loci and throughout the genome.
Maternal diet had a significant effect on the body weight of the offspring when they were fed an obesogenic diet after weaning. Our analyses showed that maternal diet had a pervasive effect on gene expression, with a pronounced effect in liver where it affected many genes involved in inflammation, cholesterol synthesis and RXR activation. We did not detect any effect of the maternal diet on DNA methylation in the liver.
Overall, our findings highlighted the persistent influence of maternal diet on adult tissue regulation and suggested that the transcriptional changes were unlikely to be caused by DNA methylation differences in adult liver.
流行病学和动物研究表明,母体饮食可影响成年后代的新陈代谢。然而,这些变化背后的分子机制仍知之甚少。在此,我们在小鼠模型中表征母体肥胖诱导的表型,并研究母体饮食在成年后代中诱导的基因表达和表观遗传变化。
我们分析了在整个孕期及产后21天由喂食高脂或低脂饮食的母鼠所生的基因相同的雄性小鼠。断奶后,每组一半的雄性小鼠喂食高脂饮食,另一半喂食低脂饮食。我们首先表征成年后代六个组织——肝脏、胰腺、白色脂肪、大脑、肌肉和心脏的全基因组基因表达模式。然后我们测量了肝脏中选定基因座及全基因组的DNA甲基化模式。
断奶后喂食致肥胖饮食时,母体饮食对后代体重有显著影响。我们的分析表明,母体饮食对基因表达有普遍影响,在肝脏中影响尤为明显,它影响了许多参与炎症、胆固醇合成和视黄酸X受体(RXR)激活的基因。我们未检测到母体饮食对肝脏DNA甲基化有任何影响。
总体而言,我们的研究结果突出了母体饮食对成年组织调节的持续影响,并表明转录变化不太可能由成年肝脏中的DNA甲基化差异引起。