Maternal epigenetic factors in embryonic and postnatal development

• Published in: Genes to cells : devoted to molecular & cellular mechanisms 2023-06, Vol.28 (6), p.422-432
• Main Authors: Nishimura, Hiromi, Ikawa, Yayoi, Kajikawa, Eriko, Shimizu‐Mizuno, Natsumi, Hiver, Sylvain, Tabata‐Okamoto, Namine, Mori, Masashi, Kitajima, Tomoya, Hayashi, Tetsutaro, Yoshimura, Mika, Umeda, Mana, Nikaido, Itoshi, Kurokawa, Mineo, Watanabe, Toshio, Hamada, Hiroshi
• Format: Article
• Language: English
• Subjects: aging; Animals; development; Embryogenesis; Embryonic Development - genetics; Epigenesis, Genetic; Epigenetics; Female; Granulosa cells; Histone Demethylases - genetics; Histone Demethylases - metabolism; Lethality; Maternal effects; maternal factor; Mice; Oocytes; Oocytes - metabolism; Pregnancy; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 1356-9597; 1365-2443
• DOI: 10.1111/gtc.13024

Maternal factors present in oocytes and surrounding granulosa cells influence early development of embryos. In this study, we searched for epigenetic regulators that are expressed in oocytes and/or granulosa cells. Some of the 120 epigenetic regulators examined were expressed specifically in oocytes and/or granulosa cells. When their expression was examined in young versus aged oocytes or granulosa cells, many were significantly up‐ or downregulated in aged cells. The maternal role of six genes in development was investigated by generating oocyte‐specific knock‐out (MKO) mice. Two genes (Mllt10, Kdm2b) did not show maternal effects on later development, whereas maternal effects were evident for Kdm6a, Kdm4a, Prdm3, and Prdm16 for MKO female mice. Offspring from Kdm6a MKO mice underwent perinatal lethality at a higher rate. Pups derived from Prdm3;Prdm16 double MKO showed a higher incidence of postnatal death. Finally, embryos derived from Kdm4a MKO mice showed early developmental defects as early as the peri‐implantation stage. These results suggest that many of maternal epigenetic regulators undergo differential expression upon aging. Some, such as Kdm4a, Kdm6a, Prdm3, and Prdm16, have maternal role in later embryonic or postnatal development. Many of epigenetic regulators are expressed in oocytes and granulosa cells, and their expression is often influenced by aging. Some of the epigenetic regulators have a maternal role in embryonic and post‐natal development.