Gestational diabetes mellitus causes genome hyper-methylation of oocyte via increased EZH2

Nat Commun. 2025 Jan 2;16(1):127. doi: 10.1038/s41467-024-55499-x.

Abstract

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.

MeSH terms

  • Animals
  • DNA (Cytosine-5-)-Methyltransferase 1* / genetics
  • DNA (Cytosine-5-)-Methyltransferase 1* / metabolism
  • DNA Methylation*
  • Diabetes, Gestational* / genetics
  • Diabetes, Gestational* / metabolism
  • Enhancer of Zeste Homolog 2 Protein* / genetics
  • Enhancer of Zeste Homolog 2 Protein* / metabolism
  • Epigenesis, Genetic
  • Female
  • Humans
  • Male
  • Mice
  • Oocytes* / metabolism
  • Pregnancy

Substances

  • Enhancer of Zeste Homolog 2 Protein
  • DNA (Cytosine-5-)-Methyltransferase 1
  • Ezh2 protein, mouse
  • Dnmt1 protein, mouse