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定量蛋白质组学分析与验证确定了母猪发情周期中的整体蛋白质谱动态变化。

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

作者信息

Xin Haiyun, Li Baohong, Meng Fanming, Hu Bin, Wang Sutian, Wang Ying, Li Jianhao

机构信息

State Key Laboratory of Swine and Poultry Breeding Industry, Guangdong Key Laboratory of Animal Breeding and Nutrition, Institute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China.

Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Maoming, China.

出版信息

Front Vet Sci. 2023 Sep 28;10:1247561. doi: 10.3389/fvets.2023.1247561. eCollection 2023.

Abstract

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 ( ≤ 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.

摘要

当前的发情检测方法通常耗时且准确性低。因此,深入了解发情周期中的生理过程有助于提高发情检测的效率和准确性。在本研究中,采用无标记采集质谱法探究猪发情周期(第-3天、第0天、第3天和第8天)期间的唾液蛋白质组图谱,并应用平行反应监测(PRM)来验证蛋白质表达的相对图谱。在无标记分析中总共鉴定出1155种蛋白质,其中115种被鉴定为不同组间的差异表达蛋白质(DEP,≤0.05)。功能注释显示,这些DEP聚集在钙离子结合、肌动蛋白细胞骨架和裂合酶活性方面。PRM验证了蛋白质表达的相对图谱,其中含PHB结构域蛋白、生长因子受体结合蛋白2、延伸因子Tu、羧肽酶D、碳酸酐酶和三叶因子3在无标记和PRM方法中均被证实是一致的。对唾液进行比较蛋白质组学分析将增加我们对母猪发情周期的了解,并为发情检测提供潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf51/10568330/99c7fc416149/fvets-10-1247561-g001.jpg

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