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Quantitative proteomic analysis and verification identify global protein profiling dynamics in pig during the estrous cycle

文献类型: 外文期刊

作者: Xin, Haiyun 1 ; Li, Baohong 1 ; Meng, Fanming 1 ; Hu, Bin 1 ; Wang, Sutian 1 ; Wang, Ying 3 ; Li, Jianhao 1 ;

作者机构: 1.Guangdong Acad Agr Sci, Inst Anim Sci, State Key Lab Swine & Poultry Breeding Ind, Guangdong Key Lab Anim Breeding & Nutr, Guangzhou, Peoples R China

2.Guangdong Lab Lingnan Modern Agr, Maoming Branch, Maoming, Peoples R China

3.Guangzhou Customs Tech Ctr, Guangzhou, Peoples R China

关键词: sow; estrus detection; saliva; quantitative proteomics; differentially expressed proteins; reproduction efficiency

期刊名称:FRONTIERS IN VETERINARY SCIENCE ( 影响因子:3.2; 五年影响因子:3.5 )

ISSN:

年卷期: 2023 年 10 卷

页码:

收录情况: SCI

摘要: The current estrus detection method is generally time-consuming and has low accuracy. As such, a deeper understanding of the physiological processes during the estrous cycle accelerates the development of estrus detection efficiency and accuracy. In this study, the label-free acquisition mass spectrometry was used to explore salivary proteome profiles during the estrous cycle (day -3, day 0, day 3, and day 8) in pigs, and the parallel reaction monitoring (PRM) was applied to verify the relative profiles of protein expression. A total of 1,155 proteins were identified in the label-free analysis, of which 115 were identified as differentially expressed proteins (DEPs) among different groups (p <= 0.05). Functional annotation revealed that the DEPs were clustered in calcium ion binding, actin cytoskeleton, and lyase activity. PRM verified the relative profiles of protein expression, in which PHB domain-containing protein, growth factor receptor-bound protein 2, elongation factor Tu, carboxypeptidase D, carbonic anhydrase, and trefoil factor 3 were confirmed to be consistent in both label-free and PRM approaches. Comparative proteomic assays on saliva would increase our knowledge of the estrous cycle in sows and provide potential methods for estrus detection.

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