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

被引:17
|
作者
Felipe-Medina, Natalia [1 ,2 ]
Gomez-H, Laura [1 ,2 ]
Condezo, Yazmine B. [1 ,2 ]
Sanchez-Martin, Manuel [3 ,4 ]
Barbero, Jose Luis [5 ]
Ramos, Isabel [1 ,2 ]
Llano, Elena [1 ,2 ,6 ]
Pendas, Alberto M. [1 ,2 ]
机构
[1] Univ Salamanca, CSIC, Ctr Invest Canc, Mol Mech Program, Salamanca 37007, Spain
[2] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, Salamanca 37007, Spain
[3] Univ Salamanca, Dept Med, Salamanca 37007, Spain
[4] Univ Salamanca, Nucleus Platform, Transgen Facil, Salamanca 37007, Spain
[5] CSIC, Ctr Invest Biol, Dept Biol Celular & Mol, Madrid, Spain
[6] Univ Salamanca, Dept Fisiol & Farmacol, Salamanca, Spain
关键词
Fertility; Spermatogenesis; Ubiquitination; Meiosis; Ubiquitin-specific protease; MALE-INFERTILITY; GENE; ASSOCIATION; MUTATIONS; SPERMATOGENESIS; POLYMORPHISMS; HAPLOTYPES; COHESIN; SYSTEM; MEN;
D O I
10.1007/s00412-019-00697-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:237 / 247
页数:11
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