精子表观遗传学与男性不育:揭开分子之谜。

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY
Maryam Hosseini, Anis Khalafiyan, Mohammadreza Zare, Haniye Karimzadeh, Basireh Bahrami, Behnaz Hammami, Mohammad Kazemi
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引用次数: 0

摘要

背景:据估计,不孕症在夫妇中的发病率为 8%至 12%。人们对不孕症的认识发生了范式转变,对不孕症主要影响女性的观念提出了挑战。现在人们认识到,即使不是大多数,也有相当一部分不孕症可归因于与男性有关的因素。导致男性生殖障碍的因素有很多,包括垂体功能失调导致的精子生成异常、睾丸恶性肿瘤、再生障碍性生殖细胞、精索静脉曲张以及环境因素:哺乳动物精子的表观遗传特征是独特而专业的。各种表观遗传因子对精子中不同水平的基因进行调控,从而影响精子的功能。精子表观遗传学的变化可能受到环境暴露等因素的影响,从而导致男性不育症的发生:总之,本综述调查了有关精子细胞表观遗传学变化机制及其与男性生殖问题相关性的最新研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sperm epigenetics and male infertility: unraveling the molecular puzzle.

Background: The prevalence of infertility among couples is estimated to range from 8 to 12%. A paradigm shift has occurred in understanding of infertility, challenging the notion that it predominantly affects women. It is now acknowledged that a significant proportion, if not the majority, of infertility cases can be attributed to male-related factors. Various elements contribute to male reproductive impairments, including aberrant sperm production caused by pituitary malfunction, testicular malignancies, aplastic germ cells, varicocele, and environmental factors.

Main body: The epigenetic profile of mammalian sperm is distinctive and specialized. Various epigenetic factors regulate genes across different levels in sperm, thereby affecting its function. Changes in sperm epigenetics, potentially influenced by factors such as environmental exposures, could contribute to the development of male infertility.

Conclusion: In conclusion, this review investigates the latest studies pertaining to the mechanisms of epigenetic changes that occur in sperm cells and their association with male reproductive issues.

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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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