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Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis

BACKGROUND: Subterranean rodents have evolved many features to adapt to their hypoxic environment. The brain is an organ that is particularly vulnerable to damage caused by exposure to hypoxic conditions. To investigate the mechanisms of adaption to a hypoxic underground environment, we carried out...

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Autores principales: Dong, Qianqian, Shi, Luye, Li, Yangwei, Jiang, Mengwan, Sun, Hong, Wang, Baishi, Cheng, Han, Zhang, Yifeng, Shao, Tian, Shi, Yuhua, Wang, Zhenlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290494/
https://www.ncbi.nlm.nih.gov/pubmed/30537924
http://dx.doi.org/10.1186/s12864-018-5318-1
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author Dong, Qianqian
Shi, Luye
Li, Yangwei
Jiang, Mengwan
Sun, Hong
Wang, Baishi
Cheng, Han
Zhang, Yifeng
Shao, Tian
Shi, Yuhua
Wang, Zhenlong
author_facet Dong, Qianqian
Shi, Luye
Li, Yangwei
Jiang, Mengwan
Sun, Hong
Wang, Baishi
Cheng, Han
Zhang, Yifeng
Shao, Tian
Shi, Yuhua
Wang, Zhenlong
author_sort Dong, Qianqian
collection PubMed
description BACKGROUND: Subterranean rodents have evolved many features to adapt to their hypoxic environment. The brain is an organ that is particularly vulnerable to damage caused by exposure to hypoxic conditions. To investigate the mechanisms of adaption to a hypoxic underground environment, we carried out a cross-species brain transcriptome analysis by RNA sequencing and identified genes that are differentially expressed between the subterranean vole Lasiopodomys mandarinus and the closely related above-ground species Lasiopodomys brandtii under chronic hypoxia [10.0% oxygen (O(2))] and normoxia (20.9% O(2)). RESULTS: A total of 355 million clean reads were obtained, including 69,611 unigenes in L. mandarinus and 69,360 in L. brandtii. A total of 235 and 92 differentially expressed genes (DEGs) were identified by comparing the hypoxic and control groups of L. mandarinus and L. brandtii, respectively. A Gene Ontology (GO) analysis showed that upregulated DEGs in both species had similar functions in response to hypoxia, whereas downregulated DEGs in L. mandarinus were enriched GO terms related to enzymes involved in aerobic reactions. In the Kyoto Encyclopedia of Genes and Genomes pathway analysis, upregulated DEGs in L. mandarinus were associated with angiogenesis and the increased O(2) transport capacity of red blood cells, whereas downregulated DEGs were associated with immune responses. On the other hand, upregulated DEGs in L. brandtii were associated with cell survival, vascular endothelial cell proliferation, and neuroprotection, while downregulated genes were related to the synaptic transmission by neurons. CONCLUSIONS: L. mandarinus actively adapts its physiological functions to hypoxic conditions, for instance by increasing O(2) transport capacity and modulating O(2) consumption. In contrast, L. brandtii reacts passively to hypoxia by decreasing overall activity in order to reduce O(2) consumption. These results provide insight into hypoxia adaptation mechanisms in subterranean rodents that may be applicable to humans living at high altitudes or operating in other O(2)-poor environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5318-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-62904942018-12-17 Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis Dong, Qianqian Shi, Luye Li, Yangwei Jiang, Mengwan Sun, Hong Wang, Baishi Cheng, Han Zhang, Yifeng Shao, Tian Shi, Yuhua Wang, Zhenlong BMC Genomics Research Article BACKGROUND: Subterranean rodents have evolved many features to adapt to their hypoxic environment. The brain is an organ that is particularly vulnerable to damage caused by exposure to hypoxic conditions. To investigate the mechanisms of adaption to a hypoxic underground environment, we carried out a cross-species brain transcriptome analysis by RNA sequencing and identified genes that are differentially expressed between the subterranean vole Lasiopodomys mandarinus and the closely related above-ground species Lasiopodomys brandtii under chronic hypoxia [10.0% oxygen (O(2))] and normoxia (20.9% O(2)). RESULTS: A total of 355 million clean reads were obtained, including 69,611 unigenes in L. mandarinus and 69,360 in L. brandtii. A total of 235 and 92 differentially expressed genes (DEGs) were identified by comparing the hypoxic and control groups of L. mandarinus and L. brandtii, respectively. A Gene Ontology (GO) analysis showed that upregulated DEGs in both species had similar functions in response to hypoxia, whereas downregulated DEGs in L. mandarinus were enriched GO terms related to enzymes involved in aerobic reactions. In the Kyoto Encyclopedia of Genes and Genomes pathway analysis, upregulated DEGs in L. mandarinus were associated with angiogenesis and the increased O(2) transport capacity of red blood cells, whereas downregulated DEGs were associated with immune responses. On the other hand, upregulated DEGs in L. brandtii were associated with cell survival, vascular endothelial cell proliferation, and neuroprotection, while downregulated genes were related to the synaptic transmission by neurons. CONCLUSIONS: L. mandarinus actively adapts its physiological functions to hypoxic conditions, for instance by increasing O(2) transport capacity and modulating O(2) consumption. In contrast, L. brandtii reacts passively to hypoxia by decreasing overall activity in order to reduce O(2) consumption. These results provide insight into hypoxia adaptation mechanisms in subterranean rodents that may be applicable to humans living at high altitudes or operating in other O(2)-poor environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5318-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-11 /pmc/articles/PMC6290494/ /pubmed/30537924 http://dx.doi.org/10.1186/s12864-018-5318-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dong, Qianqian
Shi, Luye
Li, Yangwei
Jiang, Mengwan
Sun, Hong
Wang, Baishi
Cheng, Han
Zhang, Yifeng
Shao, Tian
Shi, Yuhua
Wang, Zhenlong
Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title_full Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title_fullStr Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title_full_unstemmed Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title_short Differential responses of Lasiopodomys mandarinus and Lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
title_sort differential responses of lasiopodomys mandarinus and lasiopodomys brandtii to chronic hypoxia: a cross-species brain transcriptome analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290494/
https://www.ncbi.nlm.nih.gov/pubmed/30537924
http://dx.doi.org/10.1186/s12864-018-5318-1
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