Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania, United States of America.
PLoS Genet. 2010 Jul 22;6(7):e1001033. doi: 10.1371/journal.pgen.1001033.
Epidemiological studies have reported a higher incidence of rare disorders involving imprinted genes among children conceived using assisted reproductive technology (ART), suggesting that ART procedures may be disruptive to imprinted gene methylation patterns. We examined intra- and inter-individual variation in DNA methylation at the differentially methylated regions (DMRs) of the IGF2/H19 and IGF2R loci in a population of children conceived in vitro or in vivo. We found substantial variation in allele-specific methylation at both loci in both groups. Aberrant methylation of the maternal IGF2/H19 DMR was more common in the in vitro group, and the overall variance was also significantly greater in the in vitro group. We estimated the number of trophoblast stem cells in each group based on approximation of the variance of the binomial distribution of IGF2/H19 methylation ratios, as well as the distribution of X chromosome inactivation scores in placenta. Both of these independent measures indicated that placentas of the in vitro group were derived from fewer stem cells than the in vivo conceived group. Both IGF2 and H19 mRNAs were significantly lower in placenta from the in vitro group. Although average birth weight was lower in the in vitro group, we found no correlation between birth weight and IGF2 or IGF2R transcript levels or the ratio of IGF2/IGF2R transcript levels. Our results show that in vitro conception is associated with aberrant methylation patterns at the IGF2/H19 locus. However, very little of the inter- or intra-individual variation in H19 or IGF2 mRNA levels can be explained by differences in maternal DMR DNA methylation, in contrast to the expectations of current transcriptional imprinting models. Extraembryonic tissues of embryos cultured in vitro appear to be derived from fewer trophoblast stem cells. It is possible that this developmental difference has an effect on placental and fetal growth.
流行病学研究报告称,使用辅助生殖技术(ART)受孕的儿童中,涉及印迹基因的罕见疾病发病率较高,这表明 ART 程序可能会破坏印迹基因的甲基化模式。我们检查了体外或体内受孕的儿童中 IGF2/H19 和 IGF2R 基因座的差异甲基化区域(DMR)的 DNA 甲基化的个体内和个体间变异。我们发现两个组在两个基因座上的等位基因特异性甲基化都存在很大差异。体外组中 IGF2/H19 DMR 的母体甲基化异常更为常见,并且体外组的总体方差也显着更大。我们根据 IGF2/H19 甲基化比率的二项式分布的方差以及胎盘 X 染色体失活评分的分布,估算了每个组中的滋养层干细胞数量。这两个独立的指标均表明,与体内受孕组相比,体外组的胎盘源自更少的干细胞。来自体外组的胎盘的 IGF2 和 H19 mRNA 均显着降低。尽管体外组的平均出生体重较低,但我们没有发现出生体重与 IGF2 或 IGF2R 转录本水平或 IGF2/IGF2R 转录本水平的比值之间存在相关性。我们的研究结果表明,体外受孕与 IGF2/H19 基因座的异常甲基化模式有关。然而,与当前转录印迹模型的预期相反,H19 或 IGF2 mRNA 水平的个体内或个体间变异几乎无法用母体 DMR DNA 甲基化差异来解释。体外培养的胚胎的胚胎外组织似乎来自较少的滋养层干细胞。这种发育差异可能对胎盘和胎儿生长有影响。