Su Yi, Ren Wanlu, Ma Shikun, Meng Jun, Yao Xinkui, Zeng Yaqi, Li Zexu, Li Luling, Wang Ran, Wang Jianwen
College of Animal Science, Xinjiang Agricultural University, Xinjiang, China.
Xinjiang Key Laboratory of Equine Breeding and Exercise Physiology, Urumqi, China.
Front Genet. 2025 Aug 29;16:1651628. doi: 10.3389/fgene.2025.1651628. eCollection 2025.
This study employed Yili horses participating in a 5000-meter race as a model to investigate exercise-induced gene expression alterations in peripheral blood using whole transcriptome sequencing. Jugular vein blood samples from the three leading horses were collected pre- and immediately post-race, yielding 2,171 differentially expressed mRNAs (2,080 upregulated, 91 downregulated), 4,375 differentially expressed LncRNAs (4,354 upregulated), and 68 differentially expressed circRNAs (64 upregulated). GO/KEGG analyses demonstrated significant enrichment of differential mRNAs in transmembrane transport function and pivotal signaling pathways (cAMP, MAPK, PI3K-Akt). Differential lncRNAs targeted neuro-signaling pathways (e.g., Neuroactive ligand-receptor interaction, Calcium signaling) and developmental regulators (stem cell pluripotency). Source genes of circRNAs were enriched in axon guidance and immune-related T cell receptor signaling. Molecular functions converged on transporter/receptor activity (mRNA/lncRNA) and nucleic acid/GTP binding (circRNA source genes). The protein-protein interaction analysis identified ten central genes within the heat shock protein family, such as and . Notably, significant upregulation of and indicated their potential roles in modulating cardiac rhythm, promoting tissue repair, and maintaining calcium-phosphorus homeostasis during exercise adaptation. This study provides comprehensive overview of transcriptomic regulatory mechanisms in the blood of Yili horses, offering a molecular framework for advancing understanding of physiological adaptation to exercise and optimizing equine exercise protocols.
本研究以参加5000米比赛的伊犁马为模型,利用全转录组测序研究运动诱导的外周血基因表达变化。在比赛前和比赛结束后立即采集了前三名马匹的颈静脉血样,共获得2171个差异表达的mRNA(2080个上调,91个下调)、4375个差异表达的长链非编码RNA(lncRNA,4354个上调)和68个差异表达的环状RNA(circRNA,64个上调)。基因本体论(GO)/京都基因与基因组百科全书(KEGG)分析表明,差异mRNA在跨膜运输功能和关键信号通路(环磷酸腺苷(cAMP)、丝裂原活化蛋白激酶(MAPK)、磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-Akt))中显著富集。差异lncRNA靶向神经信号通路(如神经活性配体-受体相互作用、钙信号)和发育调节因子(干细胞多能性)。circRNA的来源基因在轴突导向和免疫相关的T细胞受体信号通路中富集。分子功能集中在转运蛋白/受体活性(mRNA/lncRNA)和核酸/GTP结合(circRNA来源基因)上。蛋白质-蛋白质相互作用分析确定了热休克蛋白家族中的10个核心基因,如……和……。值得注意的是,……和……的显著上调表明它们在运动适应过程中调节心律、促进组织修复和维持钙磷稳态方面的潜在作用。本研究全面概述了伊犁马血液中的转录组调控机制,为深入理解运动的生理适应和优化马匹运动方案提供了分子框架。