DNA甲基化和组蛋白修饰与男性生殖细胞分化相关

A. Soumya, K. Radhakrishnan, Pradeep G. Kumar
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引用次数: 0

摘要

精子发生是一个高度调控的过程,在这个过程中,未分化的精原干细胞分化成高度特化的精子细胞,能够与卵子融合形成受精卵。这是通过严格控制基因表达的调节来实现的,而基因表达的调节主要取决于DNA的可及性。DNA可及性在很大程度上取决于表观遗传修饰,包括DNA甲基化和组蛋白修饰。DNA甲基化是由DNA甲基转移酶(DNMT)催化的。dnmt的时空表达水平和功能特征被认为是男性生殖细胞中基因表达的景观。另一方面,组蛋白密码是由一系列分子定义的,这些分子在不同的位点上对各种组蛋白进行翻译后修饰。所有这些复杂的事件协调生殖细胞规格,干细胞维持,有丝分裂扩增,减数分裂起始和减数分裂后分化事件。本文综述了生殖细胞中DNA甲基化和组蛋白修饰谱的序列变化,从而导致功能性精子的产生。
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DNA Methylation and Histone Modifications Associated with Male Germ Cell Differentiation
Spermatogenesis is a highly regulated process in which undifferentiated spermatogonial stem cells differentiate to form highly specialized sperm cells capable of fusing with the ovum to form a zygote. This is achieved through tightly controlled regulation of gene expression which depends crucially on DNA accessibility. DNA accessibility is largely dependent on epigenetic modifications including DNA methylation and modifications of the histones. DNA methylation is catalysed by DNA methyltransferase (DNMT) enzymes. The spatial and temporal expression levels and functional features of the DNMTs are thought to landscape the gene expression in the male germ cells. On the other hand, the histone code is defined by an array of molecules that bring about post-translational modifications of various histones at various sites. All these intricate events orchestrate germ cell specification, stem cell maintenance, mitotic amplification, initiation of meiosis and post-meiotic differentiation events. This review summarizes the sequential changes in DNA methylation and the histone modification profiles in germ cells leading to the production of functional spermatozoa.
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