Proteomic analysis of boar sperm with differential ability of liquid preservation at 17 °C

被引:4
作者
Song, Chenglei [1 ]
Zhang, Zhe [1 ]
Wei, Yilin [1 ]
Dou, Yaqing [1 ]
Qi, Kunlong [1 ]
Li, Xiuling [1 ]
Yang, Feng [1 ]
Li, Xinjian [1 ]
Wang, Kejun [1 ]
Qiao, Ruimin [1 ]
Han, Xuelei [1 ]
机构
[1] Henan Agr Univ, Coll Anim Sci & Technol, Zhengzhou 450046, Peoples R China
关键词
Proteomic; Preservation ability; Liquid preservation at 17(degrees)C; Boar sperm; Tandem mass tag; OXIDATIVE STRESS; MEMBRANE-PROTEIN; SEMEN; QUALITY; TEMPERATURE; SPERMATOZOA; PLASMA;
D O I
10.1016/j.theriogenology.2023.11.017
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the liquid preservation ability of boar sperm is pivotal for efficient management and breeding of livestock. Although sperm proteins play an important role in semen quality and freezability, how the levels of protein change in boar sperm with different liquid preservation abilities at 17(degrees)C remains unclear. In this study, two groups of boar sperm with extreme difference in liquid preservation ability, namely the good preservation ability (GPA) and the poor preservation ability (PPA) groups, were selected by evaluating sperm motility parameters on the 7th day of liquid preservation at 17(degrees)C. Quantitative proteomics based on tandem mass tag (TMT) labeling was used, sperm proteomic characteristics from two groups were analyzed, and potentially key proteins related to the fluid preservation ability of sperm were identified. A total of 187 differentially expressed proteins (DEPs) were identified among 2791 quantified proteins, including 85 upregulated, and 102 down-regulated proteins. Further, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses of the DEPs revealed that they were enriched in GO terms associated with response to oxidative stress, enzyme activity related to oxidative stress or redox reactions, and several metabolic activities. The significant KEGG pathways included peroxisome, metabolic pathways, selenocompound metabolism, and collection duct acid secretion. In addition, analysis of protein-protein interactions further identified 8 proteins that could be used as biomarker candidates, including GPX5, GLRX, ENO4, QPCT, BBS7, OXSR1, DHRS4 and AP2S1, which may play an essential role in indicating the liquid preservation ability of boar sperm. These findings in this study provide new insights into the underlying molecular mechanisms of the liquid preservation ability of boar sperm. Moreover, the selected candidate proteins can serve as a reference for evaluating sperm quality or preservation ability in boars and their application in related biotechnologies.
引用
收藏
页码:103 / 112
页数:10
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