Wentao Zhang, Chao Yuan, Xuejiao An, Tingting Guo, Caihong Wei, Zengkui Lu, Jianbin Liu
{"title":"Genomic Insights into Tibetan Sheep Adaptation to Different Altitude Environments.","authors":"Wentao Zhang, Chao Yuan, Xuejiao An, Tingting Guo, Caihong Wei, Zengkui Lu, Jianbin Liu","doi":"10.3390/ijms252212394","DOIUrl":null,"url":null,"abstract":"<p><p>In recent years, research has gradually uncovered the mechanisms of animal adaptation to hypoxic conditions in different altitude environments, particularly at the genomic level. However, past genomic studies on high-altitude adaptation have often not delved deeply into the differences between varying altitude levels. This study conducted whole-genome sequencing on 60 Tibetan sheep (Medium Altitude Group (MA): 20 Tao sheep (TS) at 2887 m, High Altitude Group (HA): 20 OuLa sheep (OL) at 3501 m, and Ultra-High Altitude Group (UA): 20 AWang sheep (AW) at 4643 m) from different regions of the Tibetan Plateau in China to assess their responses under varying conditions. Population genetic structure analysis revealed that the three groups are genetically independent, but the TS and OL groups have experienced gene flow with other northern Chinese sheep due to geographical factors. Selection signal analysis identified <i>FGF10</i>, <i>MMP14</i>, <i>SLC25A51</i>, <i>NDUFB8</i>, <i>ALAS1</i>, <i>PRMT1</i>, <i>PRMT5</i>, and <i>HIF1AN</i> as genes associated with ultra-high-altitude hypoxia adaptation, while <i>HMOX2</i>, <i>SEMA4G</i>, <i>SLC16A2</i>, <i>SLC22A17</i>, and <i>BCL2L2</i> were linked to high-altitude hypoxia adaptation. Functional analysis showed that ultra-high-altitude adaptation genes tend to influence physiological mechanisms directly affecting oxygen uptake, such as lung development, angiogenesis, and red blood cell formation. In contrast, high-altitude adaptation genes are more inclined to regulate mitochondrial DNA replication, iron homeostasis, and calcium signaling pathways to maintain cellular function. Additionally, the functions of shared genes further support the adaptive capacity of Tibetan sheep across a broad geographic range, indicating that these genes offer significant selective advantages in coping with oxygen scarcity. In summary, this study not only reveals the genetic basis of Tibetan sheep adaptation to different altitudinal conditions but also highlights the differences in gene regulation between ultra-high- and high-altitude adaptations. These findings offer new insights into the adaptive evolution of animals in extreme environments and provide a reference for exploring adaptation mechanisms in other species under hypoxic conditions.</p>","PeriodicalId":14156,"journal":{"name":"International Journal of Molecular Sciences","volume":"25 22","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Molecular Sciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/ijms252212394","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In recent years, research has gradually uncovered the mechanisms of animal adaptation to hypoxic conditions in different altitude environments, particularly at the genomic level. However, past genomic studies on high-altitude adaptation have often not delved deeply into the differences between varying altitude levels. This study conducted whole-genome sequencing on 60 Tibetan sheep (Medium Altitude Group (MA): 20 Tao sheep (TS) at 2887 m, High Altitude Group (HA): 20 OuLa sheep (OL) at 3501 m, and Ultra-High Altitude Group (UA): 20 AWang sheep (AW) at 4643 m) from different regions of the Tibetan Plateau in China to assess their responses under varying conditions. Population genetic structure analysis revealed that the three groups are genetically independent, but the TS and OL groups have experienced gene flow with other northern Chinese sheep due to geographical factors. Selection signal analysis identified FGF10, MMP14, SLC25A51, NDUFB8, ALAS1, PRMT1, PRMT5, and HIF1AN as genes associated with ultra-high-altitude hypoxia adaptation, while HMOX2, SEMA4G, SLC16A2, SLC22A17, and BCL2L2 were linked to high-altitude hypoxia adaptation. Functional analysis showed that ultra-high-altitude adaptation genes tend to influence physiological mechanisms directly affecting oxygen uptake, such as lung development, angiogenesis, and red blood cell formation. In contrast, high-altitude adaptation genes are more inclined to regulate mitochondrial DNA replication, iron homeostasis, and calcium signaling pathways to maintain cellular function. Additionally, the functions of shared genes further support the adaptive capacity of Tibetan sheep across a broad geographic range, indicating that these genes offer significant selective advantages in coping with oxygen scarcity. In summary, this study not only reveals the genetic basis of Tibetan sheep adaptation to different altitudinal conditions but also highlights the differences in gene regulation between ultra-high- and high-altitude adaptations. These findings offer new insights into the adaptive evolution of animals in extreme environments and provide a reference for exploring adaptation mechanisms in other species under hypoxic conditions.
近年来,研究逐渐揭示了动物在不同海拔环境下对缺氧条件的适应机制,尤其是在基因组水平上。然而,以往有关高海拔适应性的基因组研究往往没有深入探讨不同海拔高度之间的差异。本研究对来自中国青藏高原不同地区的60只藏羊(中海拔组20只,海拔2887米;高海拔组20只,海拔3501米;超高海拔组20只,海拔4643米)进行了全基因组测序,以评估它们在不同条件下的反应。种群遗传结构分析表明,这三个组在遗传上是独立的,但由于地理因素,TS 组和 OL 组与其他中国北方绵羊发生了基因流动。选择信号分析发现,FGF10、MMP14、SLC25A51、NDUFB8、ALAS1、PRMT1、PRMT5和HIF1AN与超高海拔缺氧适应有关,而HMOX2、SEMA4G、SLC16A2、SLC22A17和BCL2L2与高海拔缺氧适应有关。功能分析显示,超高海拔适应基因倾向于影响直接影响摄氧量的生理机制,如肺发育、血管生成和红细胞形成。相比之下,高海拔适应基因更倾向于调节线粒体DNA复制、铁平衡和钙信号通路,以维持细胞功能。此外,共享基因的功能进一步支持了藏羊在广泛地理范围内的适应能力,表明这些基因在应对缺氧方面具有显著的选择性优势。总之,本研究不仅揭示了藏羊适应不同海拔条件的遗传基础,而且突出了超高海拔和高海拔适应基因调控的差异。这些发现为极端环境下动物的适应性进化提供了新的见解,并为探索其他物种在缺氧条件下的适应机制提供了参考。
期刊介绍:
The International Journal of Molecular Sciences (ISSN 1422-0067) provides an advanced forum for chemistry, molecular physics (chemical physics and physical chemistry) and molecular biology. It publishes research articles, reviews, communications and short notes. Our aim is to encourage scientists to publish their theoretical and experimental results in as much detail as possible. Therefore, there is no restriction on the length of the papers or the number of electronics supplementary files. For articles with computational results, the full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material (including animated pictures, videos, interactive Excel sheets, software executables and others).