Embryonic yield-related serum proteomic analysis at bovine superovulation.

IF 3.1 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2026-09-29 eCollection Date: 2026-01-01 DOI:10.3389/fvets.2026.1923597
Yongli Yue, Anping Xie, Ruilin Fang, Xvhui Hu, Yijing Zhu, Ruifang Li, Liguo Zhang, Xiaohu Su
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Abstract

Superovulation is a key technology for accelerating genetic improvement in cattle, but its efficiency is limited by the unpredictable ovarian response among donors. A non-invasive method to predict this response could enhance superovulation outcomes. As serum proteome may mirror ovarian function, this study aimed to identify potential serum protein biomarkers at critical time points to predict embryo yield in donor cows. In this study, blood samples were collected from 33 donor cows undergoing superovulation at two time points: before FSH administration (designated BS) and at estrus detection (designated E). Based on the total number of embryos recovered, the cows were subsequently assigned to high embryonic yield (HEY) and low embryonic yield (LEY) groups. Proteomic sequencing was performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). A total of 352 embryos were collected. Proteomic analysis identified 1,620 proteins, corresponding to 11,726 annotated entries. A total of 154 and 102 differentially expressed proteins were identified between HEY and LEY at BS and E, respectively (|log2FC| ≥0.263, P < 0.05, FDR<0.01). Thirteen proteins were shared between the two time points, including consistently upregulated vitamin D-binding protein (GC). The enriched pathways were mainly metabolism-related. Notably, elevated TCN2 and DNMT1 at BS (AUC = 0.96 and 1.00, respectively), and AGRN, RCN3, and WNT7B at E (AUC = 1.00, 0.80, and 0.84, respectively), were associated with the HEY group, suggesting their potential as biomarkers for predicting embryo yield in bovine superovulation. Collectively, this study identified multiple serum protein biomarkers, providing novel molecular insights into the serum protein response to superovulation and laying a foundation for the development of non-invasive prediction strategies.

牛超排卵时胚胎产量相关血清蛋白质组学分析。
超排卵是加速牛遗传改良的一项关键技术,但其效率受到供体卵巢不可预测反应的限制。一种非侵入性的方法来预测这种反应可以提高超排卵的结果。由于血清蛋白质组可以反映卵巢功能,本研究旨在确定关键时间点的潜在血清蛋白质生物标志物,以预测供体奶牛的胚胎产量。在本研究中,采集了33头供体奶牛在两个时间点(FSH给药前(指定BS)和发情检测时(指定E)进行超排卵的血液样本。根据回收胚胎总数,将奶牛分为高胚胎产量组(HEY)和低胚胎产量组(LEY)。采用液相色谱-串联质谱法(LC-MS/MS)进行蛋白质组学测序。共收集胚胎352个。蛋白质组学分析鉴定出1,620个蛋白质,对应于11,726个注释条目。在BS和E处,HEY和LEY之间共鉴定出154和102个差异表达蛋白(|log2FC|≥0.263,P < 0.05, FDR)
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来源期刊
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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