Centre de Recherche en Biologie de la Reproduction, Institut des Nutraceutiques et des Aliments Fonctionnels, Université Laval, Québec, QC, G1V 0A6, Canada.
BMC Genomics. 2013 Jun 18;14:406. doi: 10.1186/1471-2164-14-406.
It was recently established that changes in methylation during development are dynamic and involve both methylation and demethylation processes. Yet, which genomic sites are changing and what are the contributions of methylation (5mC) and hydroxymethylation (5hmC) to this epigenetic remodeling is still unknown. When studying early development, options for methylation profiling are limited by the unavailability of sufficient DNA material from these scarce samples and limitations are aggravated in non-model species due to the lack of technological platforms. We therefore sought to obtain a representation of differentially 5mC or 5hmC loci during bovine early embryo stages through the use of three complementary methods, based on selective methyl-sensitive restriction and enrichment by ligation-mediated PCR or on subtractive hybridization. Using these strategies, libraries of putative methylation and hydroxymethylated sites were generated from Day-7 and Day-12 bovine embryos.
Over 1.2 million sequencing reads were analyzed, resulting in 151,501 contigs, of which 69,136 were uniquely positioned on the genome. A total of 101,461 putative methylated sites were identified. The output of the three methods differed in genomic coverage as well as in the nature of the identified sites. The classical MspI/HpaII combination of restriction enzymes targeted CpG islands whereas the other methods covered 5mC and 5hmC sites outside of these regions. Data analysis suggests a transition of these methylation marks between Day-7 and Day-12 embryos in specific classes of repeat-containing elements.
Our combined strategy offers a genomic map of the distribution of cytosine methylation/hydroxymethylation during early bovine embryo development. These results support the hypothesis of a regulatory phase of hypomethylation in repeat sequences during early embryogenesis.
最近的研究表明,发育过程中的甲基化变化是动态的,涉及甲基化和去甲基化过程。然而,哪些基因组位点正在发生变化,以及甲基化(5mC)和羟甲基化(5hmC)对此表观遗传重塑的贡献是什么,仍然未知。在研究早期发育时,由于这些稀有样本中可用的 DNA 材料不足,以及非模式物种缺乏技术平台,甲基化分析的选择有限。因此,我们试图通过使用三种互补的方法,基于选择性甲基敏感限制和连接介导的 PCR 或差减杂交的富集,获得牛早期胚胎阶段差异 5mC 或 5hmC 位点的代表性。使用这些策略,从 Day-7 和 Day-12 的牛胚胎中生成了假定的甲基化和羟甲基化位点文库。
分析了超过 120 万个测序读段,得到了 151501 个重叠群,其中 69136 个是在基因组上唯一定位的。共鉴定出 101461 个假定的甲基化位点。这三种方法的输出在基因组覆盖范围以及鉴定出的位点的性质上存在差异。经典的 MspI/HpaII 组合限制性内切酶靶向 CpG 岛,而其他方法则覆盖了这些区域之外的 5mC 和 5hmC 位点。数据分析表明,在特定的重复元件类中,这些甲基化标记在 Day-7 和 Day-12 胚胎之间发生了转变。
我们的联合策略提供了牛早期胚胎发育过程中胞嘧啶甲基化/羟甲基化分布的基因组图谱。这些结果支持了在早期胚胎发生中重复序列去甲基化的调节阶段假说。