O'Doherty Alan M, Magee David A, O'Shea Lynee C, Forde Niamh, Beltman Marijke E, Mamo Solomon, Fair Trudee
School of Agriculture and Food Science, University College Dublin, Belfield, Dublin, Ireland.
School of Medicine and Medical Sciences, University College Dublin, Belfield, Dublin 4, Ireland.
BMC Dev Biol. 2015 Mar 10;15:13. doi: 10.1186/s12861-015-0060-2.
In mammals, maternal differentially methylated regions (DMRs) acquire DNA methylation during the postnatal growth stage of oogenesis, with paternal DMRs acquiring DNA methylation in the perinatal prospermatagonia. Following fusion of the male and female gametes, it is widely accepted that murine DNA methylation marks at the DMRs of imprinted genes are stable through embryogenesis and early development, until they are reprogrammed in primordial germ cells. However, the DNA methylation dynamics at DMRs of bovine imprinted genes during early stages of development remains largely unknown. The objective of this investigation was to analyse the methylation dynamics at imprinted gene DMRs during bovine embryo development, from blastocyst stage until implantation.
To this end, pyrosequencing technology was used to quantify DNA methylation at DMR-associated CpG dinucleotides of six imprinted bovine genes (SNRPN, MEST, IGF2R, PLAGL1, PEG10 and H19) using bisulfite-modified genomic DNA isolated from individual blastocysts (Day 7); ovoid embryos (Day 14); filamentous embryos (Day 17) and implanting conceptuses (Day 25). For all genes, the degree of DNA methylation was most variable in Day 7 blastocysts compared to later developmental stages (P < 0.05). Furthermore, mining of RNA-seq transcriptomic data and western blot analysis revealed a specific window of expression of DNA methylation machinery genes (including DNMT3A, DNMT3B, TRIM28/KAP1 and DNMT1) and proteins (DNMT3A, DNMT3A2 and DNMT3B) by bovine embryos coincident with imprint stabilization.
The findings of this study suggest that the DNA methylation status of bovine DMRs might be variable during the early stages of embryonic development, possibly requiring an active period of imprint stabilization.
在哺乳动物中,母源差异甲基化区域(DMRs)在卵子发生的出生后生长阶段获得DNA甲基化,而父源DMRs在围产期精原细胞中获得DNA甲基化。雌雄配子融合后,普遍认为印记基因DMRs处的小鼠DNA甲基化标记在胚胎发生和早期发育过程中是稳定的,直到它们在原始生殖细胞中被重编程。然而,牛印记基因DMRs在发育早期的DNA甲基化动态仍在很大程度上未知。本研究的目的是分析牛胚胎从囊胚阶段到着床期间印记基因DMRs的甲基化动态。
为此,使用焦磷酸测序技术,对从单个囊胚(第7天)、卵形胚胎(第14天)、丝状胚胎(第17天)和着床期孕体(第25天)中分离的亚硫酸氢盐修饰的基因组DNA,定量六个牛印记基因(SNRPN、MEST、IGF2R、PLAGL1、PEG10和H19)的DMR相关CpG二核苷酸处的DNA甲基化。对于所有基因,与后期发育阶段相比,第7天囊胚的DNA甲基化程度变化最大(P < 0.05)。此外,对RNA测序转录组数据的挖掘和蛋白质免疫印迹分析显示,牛胚胎表达DNA甲基化机制基因(包括DNMT3A、DNMT3B、TRIM28/KAP1和DNMT1)和蛋白质(DNMT3A、DNMT3A2和DNMT3B)的特定窗口与印记稳定一致。
本研究结果表明,牛DMRs的DNA甲基化状态在胚胎发育早期可能是可变的,可能需要一个印记稳定的活跃期。