He Zhaohua, Tian Liming, Wang Guan, Zhao Fangfang, Zhao Pengfei, Zhang Shuhong, Li Shaobin, Yang Guangli
College of Biology and Food, Shangqiu Normal University, Shangqiu 476000, China.
Gansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, International Wool Research Institute, Gansu Agricultural University, Lanzhou 730070, China.
Animals (Basel). 2025 Sep 2;15(17):2578. doi: 10.3390/ani15172578.
Fiber fineness is a critical determinant of wool quality and is of great significance in enhancing the overall quality of wool. The aim of this research was to pinpoint the key proteins that participate in the regulation of wool fineness. To achieve this, we utilized Astral-DIA proteomics technology to examine the disparities in proteins, pathways, and GO terms among the wool tissues of Gansu alpine fine-wool sheep with varying mean fiber diameters (MFD). The experiment was divided into two groups: coarse (group C, MFD = 22.36 ± 0.75 μm, = 4) and fine (group F, MFD = 16.89 ± 0.36 μm, = 4). The results indicated that 67 differentially expressed proteins (DEPs) were identified from the wool tissues of Gansu alpine fine-wool sheep in groups C and F. Functional enrichment analysis demonstrated that several key differential proteins, including MGST3, KRT26, KRT72, KRT74, KRT71, etc., were mainly enriched in multiple functional pathways. These pathways included glutathione metabolism, oxidative phosphorylation, the degradation of valine, leucine, and isoleucine, intermediate filaments, serine protease activity, and cysteine protease activity ( < 0.05). Furthermore, protein-protein interaction (PPI) network analysis suggested that type II keratin and type I keratin (such as CTSF, PSAP, TMEM106B, LYPD3, KRT71, KRT72), along with glutathione metabolism (MGST3, W5QDB7), are closely related to hair follicle development and the regulation of wool fineness. In summary, this study enriches the existing sheep proteinome database and offers novel perspectives on the regulatory mechanisms of wool fineness.
纤维细度是羊毛品质的关键决定因素,对提高羊毛整体质量具有重要意义。本研究旨在找出参与调节羊毛细度的关键蛋白质。为此,我们利用Astral-DIA蛋白质组学技术,研究了不同平均纤维直径(MFD)的甘肃高山细毛羊羊毛组织在蛋白质、信号通路和基因本体(GO)术语方面的差异。实验分为两组:粗毛组(C组,MFD = 22.36 ± 0.75 μm,n = 4)和细毛组(F组,MFD = 16.89 ± 0.36 μm,n = 4)。结果表明,从C组和F组甘肃高山细毛羊的羊毛组织中鉴定出67种差异表达蛋白(DEP)。功能富集分析表明,包括MGST3、KRT26、KRT72、KRT74、KRT71等在内的几种关键差异蛋白主要富集于多个功能通路。这些通路包括谷胱甘肽代谢、氧化磷酸化、缬氨酸、亮氨酸和异亮氨酸的降解、中间丝、丝氨酸蛋白酶活性和半胱氨酸蛋白酶活性(P < 0.05)。此外,蛋白质-蛋白质相互作用(PPI)网络分析表明,II型角蛋白和I型角蛋白(如CTSF、PSAP、TMEM106B、LYPD3、KRT71、KRT72)以及谷胱甘肽代谢(MGST3、W5QDB7)与毛囊发育和羊毛细度调节密切相关。总之,本研究丰富了现有的绵羊蛋白质组数据库,并为羊毛细度的调控机制提供了新的视角。