Ly Lundi, Chan Donovan, Landry Mylène, Angle Camille, Martel Josée, Trasler Jacquetta
Department of Human Genetics, McGill University, Montreal, QC, Canada.
Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Environ Epigenet. 2020 Nov 18;6(1):dvaa018. doi: 10.1093/eep/dvaa018. eCollection 2020.
The dynamic patterning of DNA and histone methylation during oocyte development presents a potentially susceptible time for epigenetic disruption due to early life environmental exposure of future mothers. We investigated whether maternal exposure to folic acid deficient and supplemented diets starting could affect oocytes and cause adverse developmental and epigenetic effects in next generation progeny. Female BALB/c mice (F0) were placed on one of four amino acid defined diets for 4 weeks before pregnancy and throughout gestation and lactation: folic acid control (rodent recommended daily intake; Ctrl), 7-fold folic acid deficient, 10-fold folic acid supplemented or 20-fold folic acid supplemented diets. F1 female pups were weaned onto Ctrl diets, mated to produce the F2 generation and the F2 offspring were examined at E18.5 for developmental and epigenetic abnormalities. Resorption rates were increased and litter sizes decreased amongst F2 E18.5-day litters in the 20-fold folic acid supplemented group. Increases in abnormal embryo outcomes were observed in all three folic acid deficient and supplemented groups. Subtle genome-wide DNA methylation alterations were found in the placentas and brains of F2 offspring in the 7-fold folic acid deficient , 10-fold folic acid supplemented and 20-fold folic acid supplemented groups; in contrast, global and imprinted gene methylation were not affected. The findings show that early life female environmental exposures to both low and high folate prior to oocyte maturation can compromise oocyte quality, adversely affecting offspring of the next generation, in part by altering DNA methylation patterns.
在卵母细胞发育过程中,DNA和组蛋白甲基化的动态模式表明,由于未来母亲在生命早期受到环境暴露,这一时期的表观遗传可能容易受到干扰。我们研究了从开始,母体暴露于叶酸缺乏和补充叶酸的饮食中是否会影响卵母细胞,并在下一代后代中引起不良的发育和表观遗传效应。雌性BALB/c小鼠(F0)在怀孕前4周以及整个妊娠期和哺乳期被置于四种氨基酸限定饮食之一:叶酸对照(啮齿动物推荐每日摄入量;Ctrl)、7倍叶酸缺乏、10倍叶酸补充或20倍叶酸补充饮食。F1雌性幼崽断奶后采用Ctrl饮食,交配产生F2代,并在E18.5时检查F2后代的发育和表观遗传异常情况。在20倍叶酸补充组的F2 E18.5日龄幼崽中,吸收率增加,窝仔数减少。在所有三个叶酸缺乏和补充叶酸的组中均观察到异常胚胎结局增加。在7倍叶酸缺乏、10倍叶酸补充和20倍叶酸补充组的F2后代的胎盘和大脑中发现了全基因组范围内细微的DNA甲基化改变;相比之下,整体和印迹基因甲基化未受影响。研究结果表明,在卵母细胞成熟之前,生命早期雌性暴露于低叶酸和高叶酸环境中均会损害卵母细胞质量,对下一代后代产生不利影响,部分原因是改变了DNA甲基化模式。