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超排卵改变早期胚胎发育过程中的全球 DNA 甲基化。

Superovulation alters global DNA methylation in early mouse embryo development.

机构信息

a Department of Obstetrics and Gynecology , University of Washington , Seattle , WA , USA.

b Institute for Stem Cell and Regenerative Medicine , University of Washington , Seattle , WA , USA.

出版信息

Epigenetics. 2019 Aug;14(8):780-790. doi: 10.1080/15592294.2019.1615353. Epub 2019 May 13.

Abstract

Assisted reproductive technologies are known to alter the developmental environment of gametes and early embryos during the most dynamic period of establishing the epigenome. This may result in the introduction of errors during active DNA methylation reprogramming. Controlled ovarian hyperstimulation, or superovulation, is a ubiquitously used intervention which has been demonstrated to alter the methylation of certain imprinted genes. The objective of this study was to investigate whether ovarian hyperstimulation results in genome-wide DNA methylation changes in mouse early embryos. Ovarian hyperstimulation was induced by treating mice with either low doses (5 IU) or high doses (10 IU) of PMSG and hCG. Natural mating (NM) control mice received no treatment. Zygotes and 8-cell embryos were collected from each group and DNA methylomes were generated by whole-genome bisulfite sequencing. In the NM group, mean CpG methylation levels slightly decreased from zygote to 8-cell stage, whereas a large decrease in mean CpG methylation level was observed in both superovulated groups. A separate analysis of the mean CpG methylation levels within each developmental stage confirmed that significant genome-wide erasure of CpG methylation from the zygote to 8-cell stage only occurred in the superovulation groups. Our results suggest that superovulation alters the genome-wide DNA methylation erasure process in mouse early pre-implantation embryos. It is not clear whether these changes are transient or persistent. Further studies are ongoing to investigate the impact of ovarian hyperstimulation on DNA methylation re-establishment in later stages of embryo development.

摘要

辅助生殖技术已知会在配子和早期胚胎形成表观基因组的最活跃时期改变其发育环境。这可能导致在活跃的 DNA 甲基化重编程过程中引入错误。控制性卵巢过度刺激,即超排卵,是一种广泛使用的干预措施,已被证明会改变某些印迹基因的甲基化。本研究的目的是研究卵巢过度刺激是否会导致小鼠早期胚胎的全基因组 DNA 甲基化变化。通过用低剂量(5 IU)或高剂量(10 IU) PMSG 和 hCG 处理小鼠来诱导卵巢过度刺激。自然交配(NM)对照小鼠未接受任何处理。从每个组中收集受精卵和 8 细胞胚胎,并通过全基因组亚硫酸氢盐测序生成 DNA 甲基组。在 NM 组中,从受精卵到 8 细胞阶段的平均 CpG 甲基化水平略有下降,而在两个超排卵组中观察到平均 CpG 甲基化水平的大幅下降。在每个发育阶段内对平均 CpG 甲基化水平的单独分析证实,仅在超排卵组中,从受精卵到 8 细胞阶段的全基因组 CpG 甲基化完全消除才会发生。我们的结果表明,超排卵改变了小鼠早期胚胎前植入期的全基因组 DNA 甲基化消除过程。目前尚不清楚这些变化是短暂的还是持久的。正在进行进一步的研究,以调查卵巢过度刺激对胚胎发育后期 DNA 甲基化重新建立的影响。

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