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Multiple omic investigations of freeze tolerance adaptation in the aquatic ectothermic vertebrate, the Amur sleeper

Wenqi Lv, Haifeng Jiang, Yuting Qian, Minghui Meng, Cheng Wang, Ning Sun, Yongrui Lu, Houhua Bing, Chengchi Fang, David M. Irwin, Shunping He, Liandong Yang
doi: https://doi.org/10.1101/2022.05.10.491133
Wenqi Lv
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Haifeng Jiang
2College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, China
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Yuting Qian
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Minghui Meng
6Diggers (Wuhan) Biotechnology Co., Ltd, Wuhan 430000, China
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Cheng Wang
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Ning Sun
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Yongrui Lu
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Houhua Bing
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
5University of Chinese Academy of Sciences, Beijing 100049, China
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Chengchi Fang
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
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David M. Irwin
8Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto M5S1A8, Canada
9Banting and Best Diabetes Centre, University of Toronto, Toronto M5S1A8, Canada
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Shunping He
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
3Academy of Plateau Science and Sustainability, Qinghai Normal University, Xining 810016, P. R. China
7Center for Excellence in Animal Evolution and Genetics, Chinese Academy of Sciences, Kunming 650223, China
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  • For correspondence: clad@ihb.ac.cn yangliandong1987@163.com
Liandong Yang
1The Key Laboratory of Aquatic Biodiversity and Conservation of Chinese Academy of Sciences, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
3Academy of Plateau Science and Sustainability, Qinghai Normal University, Xining 810016, P. R. China
4State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences
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  • For correspondence: clad@ihb.ac.cn yangliandong1987@163.com
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Abstract

Freeze tolerance is an amazing overwintering strategy that enables ectotherms to occupy new niches and survive in cold climates. However, the genetic basis underpinning this ecologically relevant adaptation is largely unknown. Amur sleeper is the only known freeze-tolerant fish species that can overwinter with its entire body frozen in ice. Here, we sequenced the chromosome-level genome of the Amur sleeper and performed comparative genomic, transcriptomic, and metabolomic analyses to investigate this remarkable adaptation. Phylogenetic analyses showed that the Amur sleeper diverged from its close relative with no cold hardiness about 15.07 million years ago and revealed two unusual population expansions during the glacial epochs. Integrative omics data identified a synchronous regulation of genes and metabolites involved in hypometabolism and cellular stress response, and several related genes showed strong evidence of accelerated evolution and positive selection. Potential evolutionary innovations that might aid in freezing survival were found to be associated with the dynamic rearrangement of the cytoskeleton to maintain cell viability, redistribution of water and cryoprotectants to limit cell volume reduction, and inhibition in nerve activity to facilitate dormancy, demonstrating a coordinated evolution for this complex adaptation. Overall, our work provides valuable resources and opportunities to unveil the genetic basis of freeze tolerance adaptation in ectothermic vertebrates.

Competing Interest Statement

The authors have declared no competing interest.

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Posted May 11, 2022.
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Multiple omic investigations of freeze tolerance adaptation in the aquatic ectothermic vertebrate, the Amur sleeper
Wenqi Lv, Haifeng Jiang, Yuting Qian, Minghui Meng, Cheng Wang, Ning Sun, Yongrui Lu, Houhua Bing, Chengchi Fang, David M. Irwin, Shunping He, Liandong Yang
bioRxiv 2022.05.10.491133; doi: https://doi.org/10.1101/2022.05.10.491133
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Multiple omic investigations of freeze tolerance adaptation in the aquatic ectothermic vertebrate, the Amur sleeper
Wenqi Lv, Haifeng Jiang, Yuting Qian, Minghui Meng, Cheng Wang, Ning Sun, Yongrui Lu, Houhua Bing, Chengchi Fang, David M. Irwin, Shunping He, Liandong Yang
bioRxiv 2022.05.10.491133; doi: https://doi.org/10.1101/2022.05.10.491133

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