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Maternal Choline Supplementation during Normal Murine Pregnancy Alters the Placental Epigenome: Results of an Exploratory Study

机译:正常小鼠妊娠期间的母体胆碱补充疗法可改变胎盘表观基因组:一项探索性研究的结果

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摘要

The placental epigenome regulates processes that affect placental and fetal development, and could be mediating some of the reported effects of maternal choline supplementation (MCS) on placental vascular development and nutrient delivery. As an extension of work previously conducted in pregnant mice, the current study sought to explore the effects of MCS on various epigenetic markers in the placenta. RNA and DNA were extracted from placentas collected on embryonic day 15.5 from pregnant mice fed a 1X or 4X choline diet, and were subjected to genome-wide sequencing procedures or mass-spectrometry-based assays to examine placental imprinted gene expression, DNA methylation patterns, and microRNA (miRNA) abundance. MCS yielded a higher (fold change = 1.63–2.25) expression of four imprinted genes (Ampd3, Tfpi2, Gatm and Aqp1) in the female placentas and a lower (fold change = 0.46–0.62) expression of three imprinted genes (Dcn, Qpct and Tnfrsf23) in the male placentas (false discovery rate (FDR) ≤ 0.05 for both sexes). Methylation in the promoter regions of these genes and global placental DNA methylation were also affected (p ≤ 0.05). Additionally, a lower (fold change = 0.3; Punadjusted = 2.05 × 10−4; FDR = 0.13) abundance of miR-2137 and a higher (fold change = 1.25–3.92; p < 0.05) expression of its target genes were detected in the 4X choline placentas. These data demonstrate that the placental epigenome is responsive to maternal choline intake during murine pregnancy and likely mediates some of the previously described choline-induced effects on placental and fetal outcomes.
机译:胎盘表观基因组调节影响胎盘和胎儿发育的过程,并可能介导母体补充胆碱(MCS)对胎盘血管发育和营养输送的某些报道作用。作为先前在怀孕小鼠中进行的工作的扩展,当前的研究试图探索MCS对胎盘中各种表观遗传标记的影响。从在胚胎第15.5天收集的饲喂1倍或4倍胆碱饮食的怀孕小鼠的胎盘中提取RNA和DNA,并对其进行全基因组测序程序或基于质谱的分析,以检查胎盘印迹基因表达,DNA甲基化模式,和microRNA(miRNA)丰富度。 MCS在雌性胎盘中产生四个印迹基因(Ampd3,Tfpi2,Gatm和Aqp1)的较高表达(倍数= 1.63–2.25),而在三个胎记基因(Dcn,Qpct)中较低的表达(倍数= 0.46-0.62)和Tnfrsf23)在男性胎盘中(两性的错误发现率(FDR)≤0.05)。这些基因的启动子区域的甲基化和整体胎盘DNA甲基化也受到影响(p≤0.05)。此外,miR-2137的丰度较低(倍数变化= 0.3; Punadjusted = 2.05×10 -4 ; FDR = 0.13),而较高的蛋白质(倍数变化= 1.25–3.92; p <0.05)在4X胆碱胎盘中检测到了其靶基因。这些数据表明,胎盘表观基因组在鼠怀孕期间对母体胆碱的摄入有反应,并可能介导胆碱对胎盘和胎儿结局的某些先前描述的影响。

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