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<p>Proper function and switching of regulatory elements are essential for vertebrate development and are regulated by DNA methylation. We use isoform-specific knockouts of the de novo methyltransferase Dnmt3a1 and Dnmt3a2 to probe their roles during embryogenesis and postnatal development. Mice lacking Dnmt3a1 show minimal embryonic methylation loss but are smaller and die postnatally. In contrast, <i>Dnmt3a2</i><sup><i>−/−</i></sup> mice exhibit widespread hypomethylation at enhancers, CTCF sites and imprinted genes, which are largely repaired postnatally. These mice are viable but display sporadic abnormalities including anophthalmia, hydrocephalus, hydronephrosis and male infertility due to absence of sperm. Interestingly, the fertile <i>Dnmt3a2</i><sup><i>−/−</i></sup> mice produce sperm with sporadic imprinting defects. These findings suggest that the two isoform have distinct, developmentally regulated roles, with Dnmt3a2 being crucial for maintaining proper methylation of regulatory elements, especially for enhancers, CTCF sites and imprinted genes, and preventing stochastic phenotypic outcomes after birth.</p><p></p>

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Dnmt3a2 expression during embryonic development is required for phenotypic stability

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年12月8日

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  • Minmin Liu,
  • Guillermo Urrutia,
  • Rachel Shereda,
  • Galen Hostetter,
  • Stacey L. Thomas,
  • Gangning Liang,
  • Peter A. Jones

摘要

Proper function and switching of regulatory elements are essential for vertebrate development and are regulated by DNA methylation. We use isoform-specific knockouts of the de novo methyltransferase Dnmt3a1 and Dnmt3a2 to probe their roles during embryogenesis and postnatal development. Mice lacking Dnmt3a1 show minimal embryonic methylation loss but are smaller and die postnatally. In contrast, Dnmt3a2−/− mice exhibit widespread hypomethylation at enhancers, CTCF sites and imprinted genes, which are largely repaired postnatally. These mice are viable but display sporadic abnormalities including anophthalmia, hydrocephalus, hydronephrosis and male infertility due to absence of sperm. Interestingly, the fertile Dnmt3a2−/− mice produce sperm with sporadic imprinting defects. These findings suggest that the two isoform have distinct, developmentally regulated roles, with Dnmt3a2 being crucial for maintaining proper methylation of regulatory elements, especially for enhancers, CTCF sites and imprinted genes, and preventing stochastic phenotypic outcomes after birth.