Ozturk Saffet
Department of Histology and Embryology, Akdeniz University School of Medicine, Campus, 07070, Antalya, Türkiye.
J Assist Reprod Genet. 2025 Jul 14. doi: 10.1007/s10815-025-03577-4.
Oocyt e development from non-growing to metaphase II (MII) stages is largely dependent on timely and correctly controlling gene expression. During the process of biological or postovulatory aging, the epigenetic mechanisms, particularly DNA methylation, histone methylation, and acetylation, exhibit notable changes in oocytes at various stages of development. These changes mainly result from altered expression of the related catalytic enzymes. In this review, changes in DNA methylation, histone methylation, and acetylation marks and expression of the acting enzymes in aging mammalian oocytes have been comprehensively evaluated in the light of existing studies. Potential interactions between these epigenetic mechanisms are also discussed. Finally, possible interventions to regulate them in order to mitigate the loss of female fertility in the later periods of the reproductive lifespan are reviewed.
卵母细胞从非生长阶段发育到减数分裂中期II(MII)阶段在很大程度上依赖于对基因表达的及时和正确控制。在生物衰老或排卵后衰老过程中,表观遗传机制,特别是DNA甲基化、组蛋白甲基化和乙酰化,在卵母细胞发育的各个阶段表现出显著变化。这些变化主要源于相关催化酶表达的改变。在本综述中,根据现有研究全面评估了衰老哺乳动物卵母细胞中DNA甲基化、组蛋白甲基化和乙酰化标记以及作用酶的表达变化。还讨论了这些表观遗传机制之间的潜在相互作用。最后,综述了为减轻生殖寿命后期女性生育力丧失而对其进行调控的可能干预措施。