Keleher Madeline Rose, Zaidi Rabab, Shah Shyam, Oakley M Elsa, Pavlatos Cassondra, El Idrissi Samir, Xing Xiaoyun, Li Daofeng, Wang Ting, Cheverud James M
Department of Evolution, Ecology, and Population Biology, Washington University in St. Louis, St. Louis, Missouri, United States of America.
Department of Biology, Loyola University, Chicago, Illinois, United States of America.
PLoS One. 2018 Feb 15;13(2):e0192606. doi: 10.1371/journal.pone.0192606. eCollection 2018.
We investigated maternal obesity in inbred SM/J mice by assigning females to a high-fat diet or a low-fat diet at weaning, mating them to low-fat-fed males, cross-fostering the offspring to low-fat-fed SM/J nurses at birth, and weaning the offspring onto a high-fat or low-fat diet. A maternal high-fat diet exacerbated obesity in the high-fat-fed daughters, causing them to weigh more, have more fat, and have higher serum levels of leptin as adults, accompanied by dozens of gene expression changes and thousands of DNA methylation changes in their livers and hearts. Maternal diet particularly affected genes involved in RNA processing, immune response, and mitochondria. Between one-quarter and one-third of differentially expressed genes contained a differentially methylated region associated with maternal diet. An offspring high-fat diet reduced overall variation in DNA methylation, increased body weight and organ weights, increased long bone lengths and weights, decreased insulin sensitivity, and changed the expression of 3,908 genes in the liver. Although the offspring were more affected by their own diet, their maternal diet had epigenetic effects lasting through adulthood, and in the daughters these effects were accompanied by phenotypic changes relevant to obesity and diabetes.
我们通过在断奶时将雌性近交系SM/J小鼠分为高脂饮食组或低脂饮食组,使其与低脂饮食的雄性小鼠交配,在出生时将后代交叉寄养给低脂饮食的SM/J代乳母鼠,并在断奶后将后代分为高脂或低脂饮食,来研究母源性肥胖。母源性高脂饮食加剧了高脂饮食组雌性后代的肥胖,导致它们成年后体重更重、脂肪更多、血清瘦素水平更高,同时其肝脏和心脏中伴有数十种基因表达变化和数千种DNA甲基化变化。母源性饮食尤其影响参与RNA加工、免疫反应和线粒体的基因。四分之一到三分之一的差异表达基因含有与母源性饮食相关的差异甲基化区域。后代高脂饮食减少了DNA甲基化的总体变异,增加了体重和器官重量,增加了长骨长度和重量,降低了胰岛素敏感性,并改变了肝脏中3908个基因的表达。尽管后代受自身饮食的影响更大,但其母源性饮食具有持续到成年期的表观遗传效应,在雌性后代中,这些效应伴随着与肥胖和糖尿病相关的表型变化。