Ubiquitin-specific protease 26 (USP26) is not essential for mouse gametogenesis and fertility.

IF 2.5 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chromosoma Pub Date : 2019-09-01 Epub Date: 2019-03-18 DOI:10.1007/s00412-019-00697-6
Natalia Felipe-Medina, Laura Gómez-H, Yazmine B Condezo, Manuel Sanchez-Martín, José Luis Barbero, Isabel Ramos, Elena Llano, Alberto M Pendás
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引用次数: 18

Abstract

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)在小鼠配子发生和生育中不是必需的。
泛素特异性蛋白酶26 (USP26)是一种去泛素化酶,属于USPs家族,其转录模式仅限于雄性种系。由于蛋白质泛素化是减数分裂过程中一个重要的调控机制,许多研究都集中在阐明USP26的功能及其与生育的关系。在过去的十年中,一些研究报道了USP26在非阻塞性无精子症(NOA)或严重少精子症患者中存在不同的多态性,这表明该基因可能与人类不育有关。然而,其他研究也揭示了这些和新的多态性的存在,包括无义突变,在正常精子发生的男性中也是如此。因此,结果仍有争议,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。两种不同的usp26缺失突变体的表型分析显示,雄性和雌性都具有可育性,无显性表型。精母细胞的细胞学分析显示,在突触、染色体动力学、DNA修复或重组方面没有缺陷。组织病理学分析显示,雄性和雌性小鼠的不同细胞类型分布和数量均为正态分布。最后,在生育评估中观察到正常计数。这些结果首次在体内证明了USP26在小鼠配子发生中不是必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chromosoma
Chromosoma 生物-生化与分子生物学
CiteScore
3.30
自引率
6.20%
发文量
17
审稿时长
1 months
期刊介绍: Chromosoma publishes research and review articles on the functional organization of the eukaryotic cell nucleus, with a particular emphasis on the structure and dynamics of chromatin and chromosomes; the expression and replication of genomes; genome organization and evolution; the segregation of genomes during meiosis and mitosis; the function and dynamics of subnuclear compartments; the nuclear envelope and nucleocytoplasmic interactions, and more. The scope of Chromosoma encompasses genetic, biophysical, molecular and cell biological studies. Average time from receipt of contributions to first decision: 22 days Publishes research and review articles on the functional organization of the eukaryotic cell nucleus Topics include structure and dynamics of chromatin and chromosomes; the expression and replication of genomes; genome organization and evolution; the segregation of genomes during meiosis and mitosis and more Encompasses genetic, biophysical, molecular and cell biological studies.
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