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哺乳动物配子的表观遗传衰老。

Epigenetic aging of mammalian gametes.

机构信息

Institute of Biomedical and Oral Research, Faculty of Dental Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.

出版信息

Mol Reprod Dev. 2023 Dec;90(12):785-803. doi: 10.1002/mrd.23717. Epub 2023 Nov 24.

Abstract

The process of aging refers to physiological changes that occur to an organism as time progresses and involves changes to DNA, proteins, metabolism, cells, and organs. Like the rest of the cells in the body, gametes age, and it is well established that there is a decline in reproductive capabilities in females and males with aging. One of the major pathways known to be involved in aging is epigenetic changes. The epigenome is the multitude of chemical modifications performed on DNA and chromatin that affect the ability of chromatin to be transcribed. In this review, we explore the effects of aging on female and male gametes with a focus on the epigenetic changes that occur in gametes throughout aging. Quality decline in oocytes occurs at a relatively early age. Epigenetic changes constitute an important part of oocyte aging. DNA methylation is reduced with age, along with reduced expression of DNA methyltransferases (DNMTs). Histone deacetylases (HDAC) expression is also reduced, and a loss of heterochromatin marks occurs with age. As a consequence of heterochromatin loss, retrotransposon expression is elevated, and aged oocytes suffer from DNA damage. In sperm, aging affects sperm number, motility and fecundity, and epigenetic changes may constitute a part of this process. 5 methyl-cytosine (5mC) methylation is elevated in sperm from aged men, but methylation on Long interspersed nuclear elements (LINE) elements is reduced. Di and trimethylation of histone 3 lysine 9 (H3K9me2/3) is reduced in sperm from aged men and trimethylation of histone 3 lysine 27 (H3K27me3) is elevated. The protamine makeup of sperm from aged men is also changed, with reduced protamine expression and a misbalanced ratio between protamine proteins protamine P1 and protamine P2. The study of epigenetic reproductive aging is recently gaining interest. The current status of the field suggests that many aspects of gamete epigenetic aging are still open for investigation. The clinical applications of these investigations have far-reaching consequences for fertility and sociological human behavior.

摘要

衰老过程是指生物体随着时间的推移而发生的生理变化,涉及到 DNA、蛋白质、代谢、细胞和器官的变化。与体内其他细胞一样,配子也会衰老,并且已经确定随着年龄的增长,女性和男性的生殖能力会下降。已知参与衰老的主要途径之一是表观遗传变化。表观基因组是 DNA 和染色质上进行的多种化学修饰,这些修饰会影响染色质转录的能力。在这篇综述中,我们探讨了衰老对雌性和雄性配子的影响,重点关注了整个衰老过程中配子发生的表观遗传变化。卵母细胞的质量下降发生在相对较早的年龄。表观遗传变化是卵母细胞衰老的重要组成部分。随着年龄的增长,DNA 甲基化减少,同时 DNA 甲基转移酶 (DNMTs) 的表达减少。组蛋白去乙酰化酶 (HDAC) 的表达也减少,异染色质标记随着年龄的增长而丢失。由于异染色质的丢失,逆转座子的表达升高,衰老的卵母细胞会遭受 DNA 损伤。在精子中,衰老会影响精子数量、活力和生育能力,而表观遗传变化可能构成这一过程的一部分。老年男性精子中的 5 甲基胞嘧啶 (5mC) 甲基化增加,但长散布核元件 (LINE) 元件上的甲基化减少。高龄男性精子中组蛋白 3 赖氨酸 9 (H3K9me2/3) 的二甲基和三甲基化减少,组蛋白 3 赖氨酸 27 (H3K27me3) 的三甲基化增加。高龄男性精子中的鱼精蛋白组成也发生了变化,鱼精蛋白表达减少,鱼精蛋白 P1 和鱼精蛋白 P2 之间的比例失衡。生殖衰老的表观遗传研究最近引起了人们的兴趣。该领域的现状表明,配子表观遗传衰老的许多方面仍有待研究。这些研究的临床应用对生育能力和社会学人类行为有着深远的影响。

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