Wang Shengnan, Qin Zihan, Liu Juan, Liu Jie, Xiong Qiaohua, Wei Zexiao, Wang Li, Cao Yuming
Department of Obstetrics and Gynecology, Perinatal Medical Center, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, PR China.
Department of Obstetrics and Gynecology, Perinatal Medical Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Cell Death Discov. 2025 May 23;11(1):251. doi: 10.1038/s41420-025-02432-w.
Male infertility is primarily caused by impaired flagella development, reduced sperm count, and decreased motility. Despite the involvement of many genes in spermatogenesis, the precise processes remain unclear. The critical E3 ubiquitin ligase Rnf126 regulates essential cellular processes through ubiquitination-induced protein degradation. It plays a significant role in DNA repair, immune response, and signaling cascades, underscoring its central importance in maintaining cellular homeostasis. However, the mechanisms by which Rnf126 controls spermatogenesis are not fully understood. This research identifies Rnf126 as a crucial component in sperm flagellar biogenesis and germ cell development. Through genetic lineage tracing, we show that RNF126 is highly expressed in sperm cells and weakly expressed in Sertoli cells. The germ epithelium of RNF126 deficiencies is characterized by a loss of germ cells due to an increase in germ cell apoptosis at various stages of development, which ultimately results in vesiculation of the spermatogenic tubule. Targeting Rnf126 results in different types of germ cells reduction, infertility, and microtubule-associated motor activity failure (MMAF), characterized by spermatozoa with truncated, twisted, and malformed flagella. Detailed ultrastructural studies reveal the extent of flagellar damage in the absence of Rnf126, highlighting its critical role in maintaining flagellar stability. An important finding is the interaction between RNF126 and BAG6, which regulates sperm synthesis and germ cell development. Clinically, reduced RNF126 levels in sperm from individuals with oligoasthenoteratospermia are significantly different from those in fertile individuals. Investigating Rnf126 function in spermatogenesis, together with empirical findings on MMAF presentation, may improve our understanding of the developmental processes involved in sperm flagellum formation and contribute to elucidating the causes of male infertility.
男性不育主要由鞭毛发育受损、精子数量减少和活力下降引起。尽管许多基因参与精子发生过程,但其确切机制仍不清楚。关键的E3泛素连接酶Rnf126通过泛素化诱导的蛋白质降解来调节基本的细胞过程。它在DNA修复、免疫反应和信号级联反应中发挥重要作用,突显了其在维持细胞内稳态中的核心重要性。然而,Rnf126控制精子发生的机制尚未完全了解。本研究确定Rnf126是精子鞭毛生物发生和生殖细胞发育的关键组成部分。通过遗传谱系追踪,我们发现RNF126在精子细胞中高表达,而在支持细胞中弱表达。RNF126缺陷的生殖上皮特征是由于在发育的各个阶段生殖细胞凋亡增加导致生殖细胞丢失,最终导致生精小管空泡化。靶向Rnf126会导致不同类型的生殖细胞减少、不育以及微管相关运动活性衰竭(MMAF),其特征是精子鞭毛截断、扭曲和畸形。详细的超微结构研究揭示了缺乏Rnf126时鞭毛损伤的程度,突出了其在维持鞭毛稳定性中的关键作用。一个重要发现是RNF126与BAG6之间的相互作用,后者调节精子合成和生殖细胞发育。临床上,少弱畸精子症患者精子中RNF126水平降低与可育个体有显著差异。研究Rnf126在精子发生中的功能,以及关于MMAF表现的实证研究结果,可能会增进我们对精子鞭毛形成所涉及的发育过程的理解,并有助于阐明男性不育的原因。