Transcriptome analysis of five-toed jerboa organs reveals high-altitude adaptation mechanisms.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Shan-Shan Sun, Hao-Ting Zhang, Hai-Wen Yan, Xiao-Yu Kang, Qi-Qige Buren, Qian-Cheng Wang, Ming Ming, Jie-Ru Feng, Na Zhu, Xin Li, Yu Ling, Dong Zhang, Xiao-Dong Wu, Shuai Yuan, He-Ping Fu
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引用次数: 0

Abstract

High-altitude environments are characterised by extreme conditions, including hypoxia, low temperatures, and intense ultraviolet radiation. Mammals inhabiting these environments have evolved unique adaptive mechanisms, the study of which elucidates survival strategies and evolutionary pathways under extreme conditions. Understanding how native high-altitude animals respond to such environments is highly important. This study investigated the high-altitude adaptation mechanisms of the five-toed jerboa (Orientallactaga sibirica) distributed in Qinghai Province (4229 m) and Hebei Province (498 m), China, through comparative transcriptomic analysis of heart, lung, and kidney tissues. The results revealed greater mRNA transcriptional differences in the lung tissue than in the heart and kidney tissues of high-altitude jerboas, indicating heightened lung sensitivity to high-altitude conditions. In lung tissue, high-altitude jerboas show differential expression of genes related to the Complement and Coagulation cascades, Heme binding, Oxidation-reduction process (such as MASP1, A2M, SERPING1, CD55, FGA, C5AR1, and KNG1), which may be associated with modulating immune functions to mitigate hypobaric hypoxia, intense radiation, and cold-induced damage and reducing thrombosis and inflammation risks. Heart tissue exhibits differential expression of Oxidative phosphorylation and Lipid metabolism genes (such as NDUFC2, NDUFA3, NDUFS4, COX4I2, PAFAH1B3, SGMS2 and PPAR2B), which may help maintain energy equilibrium under hypoxic and cold challenges. Kidney tissue exhibits differential enrichment of pathways such as arachidonic acid metabolism and steroid hormone biosynthesis mediated by genes including CYP4A11, CYP2C29, GPX2, PTGDS, CBR1, and UGT2B31, which may help coordinate vascular regulation, immune response, and oxidative balance to maintain systemic homeostasis. These pathways and genes are differentially enriched and expressed between high-altitude and low-altitude five-toed jerboas, which may be candidates for further functional studies of plateau environmental adaptability. Our findings provide candidate genes and pathways for intraspecies adaptations across microenvironments and highlight the need for further functional validation.

Abstract Image

Abstract Image

Abstract Image

五趾跳鼠器官转录组分析揭示高原适应机制。
高海拔环境的特点是极端条件,包括缺氧、低温和强烈的紫外线辐射。生活在这些环境中的哺乳动物进化出了独特的适应机制,对其的研究阐明了极端条件下的生存策略和进化途径。了解本地高海拔动物对这种环境的反应是非常重要的。本研究通过对青海(4229 m)和河北(498 m)五趾跳鼠(Orientallactaga sibirica)心脏、肺和肾脏组织的转录组学比较分析,探讨了它们的高原适应机制。结果显示,高原跳鼠肺组织mRNA转录差异大于心脏和肾脏组织,表明肺对高海拔环境的敏感性更高。在肺组织中,高原跳鼠表现出与补体和凝血级联、血红素结合、氧化还原过程相关的基因(如MASP1、A2M、SERPING1、CD55、FGA、C5AR1和KNG1)的差异表达,这可能与调节免疫功能以减轻低压缺氧、强辐射和冷诱导损伤以及降低血栓和炎症风险有关。心脏组织表现出氧化磷酸化和脂质代谢基因(如NDUFC2、NDUFA3、NDUFS4、COX4I2、PAFAH1B3、SGMS2和PPAR2B)的差异表达,这可能有助于在缺氧和寒冷挑战下维持能量平衡。肾组织中存在由CYP4A11、CYP2C29、GPX2、PTGDS、CBR1、UGT2B31等基因介导的花生四烯酸代谢和类固醇激素生物合成等不同富集途径,这些途径可能有助于协调血管调节、免疫反应和氧化平衡,以维持系统稳态。这些通路和基因在高海拔和低海拔五趾跳鼠之间的富集和表达存在差异,这可能是高原环境适应功能研究的候选者。我们的发现为跨微环境的种内适应提供了候选基因和途径,并强调了进一步功能验证的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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