羌族(Equus kiang)染色体组水平的基因组组装揭示了其高海拔适应性的基因组基础。

IF 3.5 1区 生物学 Q1 ZOOLOGY Integrative zoology Pub Date : 2023-12-27 DOI:10.1111/1749-4877.12795
Chuang Zhou, Xiaofeng Zheng, Kexin Peng, Kaize Feng, Bisong Yue, Yongjie Wu
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引用次数: 0

摘要

羌马(Equus kiang)只能在青藏高原观察到。羌马在高海拔环境中表现出优异的运动能力,这引起了人们对其对极端环境潜在适应机制研究的广泛兴趣。在此,我们基于Hi-C测序技术构建了羌猿染色体组水平的基因组。结果表明,羌猴的染色体组水平基因组包含26条染色体(25+X),支架N50为101.77 Mb。基因组同源分析揭示了马属物种进化过程中大规模的染色体重排。系统发育和分化分析表明,羌马是驴的姊妹支,大约在13.5 Mya时从共同祖先分化而来。扩展的基因家族主要与缺氧反应、新陈代谢和免疫有关。羌人失去了大量与嗅觉有关的基因,这可能表明嗅觉灵敏度下降。在羌族中检测到的阳性选择基因(PSGs)主要与缺氧反应有关。特别是在低氧诱导因子1信号通路的STAT3基因中,有两个物种特异性的错义氨基酸突变,这可能在羌族的高海拔适应过程中发挥了重要作用。此外,还发现了羌族基因组的结构变异,这可能是羌族高海拔适应的原因之一。比较分析发现,羌族基因组中存在大量物种特异性的插入和缺失,如PIK3CB和AKT在内含子区分别有3258和189 bp的插入,可能会影响缺氧相关下游通路的表达和调控。这项研究提供了宝贵的基因组资源,我们的发现有助于更好地了解羌族对高海拔环境的基本适应策略。
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Chromosome-level genome assembly of the kiang (Equus kiang) illuminates genomic basis for its high-altitude adaptation.

The kiang (Equus kiang) can only be observed in the Qinghai-Tibet Plateau (QTP). The kiang displayed excellent athletic performance in the high-altitude environment, which attracted wide interest in the investigation of the potential adaptive mechanisms to the extreme environment. Here, we assembled a chromosome-level genome of the kiang based on Hi-C sequencing technology. A total of 324.14 Gb clean data were generated, and the chromosome-level genome with 26 chromosomes (25 + X) and scaffold N50 of 101.77 Mb was obtained for the kiang. The genomic synteny analysis revealed large-scale chromosomal rearrangement during the evolution process of Equus species. Phylogenetic and divergence analyses revealed that the kiang was the sister branch to the ass and diverged from a common ancestor at approximately 13.5 Mya. The expanded gene families were mainly related to the hypoxia response, metabolism, and immunity. The kiang suffered a significant loss of olfaction-related genes, which might indicate decreased olfactory sensibility. Positively selected genes (PSGs) detected in the kiang were mainly associated with hypoxia response. Especially, there were two species-specific missense amino acid mutations in the PSG STAT3 annotated in the hypoxia-inducible factor 1 signal pathway, which may play an important role in the high-altitude adaptation of the kiang. Moreover, structure variations in the kiang genome were also identified, which possibly contributed to the high-altitude adaptation of the kiang. Comparative analysis revealed a lot of species-specific insertions and deletions in the kiang genome, such as PIK3CB and AKT with 3258 and 189 bp insertions in the intron region, respectively, possibly affecting the expression and regulation of hypoxia-related downstream pathways. This study provided valuable genomic resources, and our findings help a better understanding of the underlying adaptive strategies to the high-altitude environment in the kiang.

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来源期刊
CiteScore
6.40
自引率
12.10%
发文量
81
审稿时长
>12 weeks
期刊介绍: The official journal of the International Society of Zoological Sciences focuses on zoology as an integrative discipline encompassing all aspects of animal life. It presents a broader perspective of many levels of zoological inquiry, both spatial and temporal, and encourages cooperation between zoology and other disciplines including, but not limited to, physics, computer science, social science, ethics, teaching, paleontology, molecular biology, physiology, behavior, ecology and the built environment. It also looks at the animal-human interaction through exploring animal-plant interactions, microbe/pathogen effects and global changes on the environment and human society. Integrative topics of greatest interest to INZ include: (1) Animals & climate change (2) Animals & pollution (3) Animals & infectious diseases (4) Animals & biological invasions (5) Animal-plant interactions (6) Zoogeography & paleontology (7) Neurons, genes & behavior (8) Molecular ecology & evolution (9) Physiological adaptations
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