Iqbal Muhammad Arsalan, Hadlich Frieder, Reyer Henry, Oster Michael, Trakooljul Nares, Wimmers Klaus, Ponsuksili Siriluck
Integrative Genomics, Research Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Faculty of Agricultural and Environmental Sciences, University Rostock, Rostock, Germany.
Front Mol Neurosci. 2025 Sep 3;18:1616363. doi: 10.3389/fnmol.2025.1616363. eCollection 2025.
Stress involves complex interactions between the brain and endocrine systems, but the gene-level processes and genetic factors mediating these responses remain unclear. This study investigates gene expression patterns and allele-specific expression (ASE) in key limbic, diencephalon and endocrine tissues to better understand stress adaptation at the molecular level.
We performed RNA sequencing on 48 samples from six distinct tissues: amygdala, hippocampus, thalamus, hypothalamus, pituitary gland, and adrenal gland. These tissues were categorized into three functionally and anatomically distinct groups: limbic (amygdala, hippocampus), diencephalon (thalamus, hypothalamus), and endocrine (pituitary, adrenal). Differential expression analyses were conducted both between individual tissues and across these tissue groups. Weighted Gene Co-expression Network Analysis (WGCNA) was applied exclusively at the tissue group level to identify group-specific gene networks. Allele-specific expression (ASE) was analyzed at the individual tissue level to capture cis-regulatory variation with high resolution.
Thirty-three candidate genes were differentially expressed across all tissues, indicating a core set involved in stress responses. Weighted Gene Co-expression Network Analysis revealed limbic and diencephalon modules enriched in neural signaling pathways such as neuroactive ligand-receptor interaction and synaptic functions, while endocrine modules were enriched for hormone biosynthesis and secretion, including thyroid and growth hormone pathways. Over 1,000 genes per tissue showed ASE, with 37 genes consistently colocalized. Ten of these displayed differences in allelic ratios, with seven (, and ) identified as eQTLs in pig brain tissue within the FarmGTEx database.
The findings reveal significant genetic regulation differences between brain and endocrine tissues, emphasizing the complexity of stress adaptation. By identifying key genes and pathways, this study provides insights that could aid in enhancing animal welfare and productivity through targeted modulation of stress-related molecular pathways.
应激涉及大脑与内分泌系统之间的复杂相互作用,但介导这些反应的基因水平过程和遗传因素仍不清楚。本研究调查关键边缘系统、间脑和内分泌组织中的基因表达模式和等位基因特异性表达(ASE),以更好地从分子水平理解应激适应。
我们对来自六个不同组织(杏仁核、海马体、丘脑、下丘脑、垂体和肾上腺)的48个样本进行了RNA测序。这些组织被分为三个功能和解剖学上不同的组:边缘系统(杏仁核、海马体)、间脑(丘脑、下丘脑)和内分泌(垂体、肾上腺)。在各个组织之间以及这些组织组之间进行了差异表达分析。加权基因共表达网络分析(WGCNA)仅在组织组水平应用,以识别组特异性基因网络。在个体组织水平分析等位基因特异性表达(ASE),以高分辨率捕获顺式调控变异。
33个候选基因在所有组织中差异表达,表明存在一组参与应激反应的核心基因。加权基因共表达网络分析显示,边缘系统和间脑模块富含神经活性配体-受体相互作用和突触功能等神经信号通路,而内分泌模块富含激素生物合成和分泌,包括甲状腺和生长激素通路。每个组织超过1000个基因显示ASE,其中37个基因始终共定位。其中10个在等位基因比例上存在差异,7个(,和)在FarmGTEx数据库中的猪脑组织中被鉴定为eQTL。
研究结果揭示了大脑和内分泌组织之间显著的遗传调控差异,强调了应激适应的复杂性。通过识别关键基因和通路,本研究提供的见解有助于通过针对性调节应激相关分子通路来提高动物福利和生产力。