The Role of N6-methyladenosine Modification in Gametogenesis and Embryogenesis: Impact on Fertility.

Yujie Wang, Chen Yang, Hanxiao Sun, Hui Jiang, Pin Zhang, Yue Huang, Zhenran Liu, Yaru Yu, Zuying Xu, Huifen Xiang, Chengqi Yi
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Abstract

The most common epigenetic modification of messenger RNAs (mRNAs) is N6-methyladenosine (m6A), which is mainly located near the 3' untranslated region of mRNAs, near the stop codons, and within internal exons. The biological effect of m6A is dynamically modulated by methyltransferases (writers), demethylases (erasers), and m6A-binding proteins (readers). By controlling post-transcriptional gene expression, m6A has a significant impact on numerous biological functions, including RNA transcription, translation, splicing, transport, and degradation. Hence, m6A influences various physiological and pathological processes, such as spermatogenesis, oogenesis, embryogenesis, placental function, and human reproductive system diseases. During gametogenesis and embryogenesis, genetic material undergoes significant changes, including epigenomic modifications such as m6A. From spermatogenesis and oogenesis to the formation of an oosperm and early embryogenesis, m6A changes occur at every step. m6A abnormalities can lead to gamete abnormalities, developmental delays, impaired fertilization, and maternal-to-zygotic transition blockage. Both mice and humans with abnormal m6A modifications exhibit impaired fertility. In this review, we discuss the dynamic biological effects of m6A and its regulators on gamete and embryonic development and review the possible mechanisms of infertility caused by m6A changes. We also discuss the drugs currently used to manipulate m6A and provide prospects for the prevention and treatment of infertility at the epigenetic level.

N6-甲基腺苷修饰在配子发生和胚胎发生中的作用:对生育能力的影响
信使核糖核酸(mRNA)最常见的表观遗传修饰是 N6-甲基腺苷(m6A),它主要位于 mRNA 的 3' 非翻译区、终止密码子附近和内部外显子内。甲基化转移酶(写入者)、去甲基化酶(擦除者)和 m6A 结合蛋白(读取者)会动态地改变 m6A 的生物效应。通过控制转录后基因的表达,m6A 对许多生物功能(包括 RNA 转录、翻译、剪接、运输和降解)都有重要影响。因此,m6A 影响着精子发生、卵子生成、胚胎发育、胎盘功能和人类生殖系统疾病等各种生理和病理过程。在配子发生和胚胎发生过程中,遗传物质会发生重大变化,包括表观基因组修饰,如 m6A。m6A 异常可导致配子异常、发育迟缓、受精能力受损以及母体到子代的转换受阻。m6A修饰异常的小鼠和人类都表现出生育能力受损。在这篇综述中,我们讨论了 m6A 及其调节因子对配子和胚胎发育的动态生物效应,并回顾了 m6A 变化导致不育的可能机制。我们还讨论了目前用于操纵 m6A 的药物,并展望了在表观遗传学水平上预防和治疗不孕症的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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