妊娠期糖尿病
卵母细胞
糖尿病
甲基化
EZH2型
基因组
生物
DNA甲基化
医学
遗传学
生物信息学
怀孕
妊娠期
基因
内分泌学
胚胎
基因表达
作者
Hongyan Guo,Shoubin Tang,Lijun Li,Jing Lin,Tingting Zhang,Shuo Chao,Xiao-Wen Jin,Kuipeng Xu,Xiaofeng Su,Shen Yin,Ming‐Hui Zhao,Gui‐An Huang,Lijia Yang,Wei Shen,Lei Zhang,Cuilian Zhang,Qing‐Yuan Sun,Zhao‐Jia Ge
标识
DOI:10.1038/s41467-024-55499-x
摘要
Gestational diabetes mellitus (GDM), a common pregnancy disease, has long-term negative effects on offspring health. Epigenetic changes may have important contributions to that, but the underlying mechanisms are not well understood. Here, we report the influence of GDM on DNA methylation of offspring (GDF1) oocytes and the possible mechanisms. Our results show that GDM induces genomic hyper-methylation of offspring oocytes, and at least a part of the altered methylation is inherited by F2 oocytes, which may be a reason for the inheritance of metabolic disorders. We further find that GDM exposure increases the expression of Ezh2 in oocytes. Ezh2 regulates DNA methylation via DNMT1, and Ezh2 knockdown reduces the genomic methylation level of GDF1 oocytes. These results suggest that GDM may induce oocyte genomic hyper-methylation of offspring via enhancing the Ezh2 expression recruiting more DNMT1 into nucleus. Gestational diabetes milletus (GDM) may have impairments on offspring health. Here, the authors suggest that the increase of EZH2 is an important reason for the disrupted DNA methylome in oocytes exposed to GDM, which may be associated with the transgenerational inheritance of the metabolic disorders.
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