Department of Human Genetics, University of Michigan, Ann Arbor, MI, United States.
Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI, United States.
Front Endocrinol (Lausanne). 2022 Jun 22;13:895502. doi: 10.3389/fendo.2022.895502. eCollection 2022.
Male fertility throughout life hinges on the successful production of motile sperm, a developmental process that involves three coordinated transitions: mitosis, meiosis, and spermiogenesis. Germ cells undergo both mitosis and meiosis to generate haploid round spermatids, in which histones bound to the male genome are replaced with small nuclear proteins known as protamines. During this transformation, the chromatin undergoes extensive remodeling to become highly compacted in the sperm head. Despite its central role in spermiogenesis and fertility, we lack a comprehensive understanding of the molecular mechanisms underlying the remodeling process, including which remodelers/chaperones are involved, and whether intermediate chromatin proteins function as discrete steps, or unite simultaneously to drive successful exchange. Furthermore, it remains largely unknown whether more nuanced interactions instructed by protamine post-translational modifications affect chromatin dynamics or gene expression in the early embryo. Here, we bring together past and more recent work to explore these topics and suggest future studies that will elevate our understanding of the molecular basis of the histone-to-protamine exchange and the underlying etiology of idiopathic male infertility.
男性的生育能力取决于能否成功生成游动精子,这一发育过程涉及三个协调的转变:有丝分裂、减数分裂和精子形成。生殖细胞经历有丝分裂和减数分裂,产生单倍体圆形精子细胞,在此过程中,与雄性基因组结合的组蛋白被称为鱼精蛋白的小核蛋白取代。在此转化过程中,染色质经历广泛的重塑,在精子头部变得高度紧凑。尽管它在精子形成和生育能力中起着核心作用,但我们缺乏对重塑过程背后的分子机制的全面了解,包括涉及哪些重塑因子/伴侣蛋白,以及中间染色质蛋白是否作为离散步骤发挥作用,还是同时联合起来推动成功的交换。此外,组蛋白到鱼精蛋白的转换过程中是否存在更细微的相互作用,这些相互作用是否影响早期胚胎中的染色质动力学或基因表达,在很大程度上仍然未知。在这里,我们汇集了过去和最近的工作来探讨这些主题,并提出未来的研究将提高我们对组蛋白到鱼精蛋白交换的分子基础以及特发性男性不育症的潜在病因的理解。