Felipe-Medina Natalia, Gómez-H Laura, Condezo Yazmine B, Sanchez-Martín Manuel, Barbero José Luis, Ramos Isabel, Llano Elena, Pendás Alberto M
Molecular Mechanisms Program, Centro de Investigación del Cáncer and Instituto de Biología Molecular y Celular del Cáncer (CSIC-Universidad de Salamanca), 37007, Salamanca, Spain.
Departamento de Medicina, Universidad de Salamanca, Salamanca, 37007, Spain.
Chromosoma. 2019 Sep;128(3):237-247. doi: 10.1007/s00412-019-00697-6. Epub 2019 Mar 18.
Ubiquitin-specific protease 26 (USP26) is a deubiquitylating enzyme belonging to the USPs family with a transcription pattern restricted to the male germline. Since protein ubiquitination is an essential regulatory mechanism during meiosis, many efforts have been focused on elucidating the function of USP26 and its relationship with fertility. During the last decade, several studies have reported the presence of different polymorphisms in USP26 in patients with non-obstructive azoospermia (NOA) or severe oligozoospermia suggesting that this gene may be associated with human infertility. However, other studies have revealed the presence of these and novel polymorphisms, including nonsense mutations, in men with normal spermatogenesis as well. Thus, the results remain controversial and its function is unknown. In the present study, we describe the in vivo functional analysis of mice lacking USP26. The phenotypic analysis of two different Usp26-null mutants showed no overt-phenotype with both males and females being fertile. Cytological analysis of spermatocytes showed no defects in synapsis, chromosome dynamics, DNA repair, or recombination. Histopathological analysis revealed a normal distribution and number of the different cell types in both male and female mice. Finally, normal counts were observed in fertility assessments. These results represent the first in vivo evidence showing that USP26 is not essential for mouse gametogenesis.
泛素特异性蛋白酶26(USP26)是一种去泛素化酶,属于泛素特异性蛋白酶(USP)家族,其转录模式仅限于雄性生殖系。由于蛋白质泛素化是减数分裂过程中一种重要的调控机制,许多研究致力于阐明USP26的功能及其与生育力的关系。在过去十年中,多项研究报告称,非梗阻性无精子症(NOA)或严重少精子症患者的USP26存在不同的多态性,这表明该基因可能与人类不育有关。然而,其他研究也发现,精子发生正常的男性也存在这些多态性以及新的多态性,包括无义突变。因此,结果仍存在争议,其功能尚不清楚。在本研究中,我们描述了缺乏USP26的小鼠的体内功能分析。对两种不同的USP26基因敲除突变体的表型分析表明,无论雄性还是雌性都没有明显的表型,且都具有生育能力。精母细胞的细胞学分析显示,在联会、染色体动态、DNA修复或重组方面没有缺陷。组织病理学分析显示,雄性和雌性小鼠中不同细胞类型的分布和数量均正常。最后,在生育力评估中观察到正常的计数。这些结果代表了首个体内证据,表明USP26对小鼠配子发生并非必不可少。