Maternal epigenetic factors in embryonic and postnatal development.
Hiromi NishimuraYayoi IkawaEriko KajikawaNatsumi Shimizu-MizunoSylvain HiverNamine Tabata-OkamotoMasashi MoriTomoya S KitajimaTetsutaro HayashiMika YoshimuraMana UmedaItoshi NikaidoMineo KurokawaToshio WatanabeHiroshi HamadaPublished in: Genes to cells : devoted to molecular & cellular mechanisms (2023)
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. This article is protected by copyright. All rights reserved.
Keyphrases
- induced apoptosis
- cell cycle arrest
- birth weight
- dna methylation
- pregnancy outcomes
- gene expression
- endoplasmic reticulum stress
- preterm infants
- type diabetes
- transcription factor
- pregnant women
- signaling pathway
- genome wide
- high fat diet induced
- cell proliferation
- pi k akt
- skeletal muscle
- high fat diet
- preterm birth