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Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac)
Vulpesare widely distributed throughout the world and have undergone drastic physiological and phenotypic changes in response to their environment. However, little is known about the underlying genetic causes of these traits, especially Vulpes corsac. In this study, RNA‐Seq was used to obtain a comp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019142/ https://www.ncbi.nlm.nih.gov/pubmed/35462974 http://dx.doi.org/10.1002/ece3.8866 |
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author | Yang, Xiufeng Sun, Guolei Xia, Tian Cha, Muha Zhang, Lei Pang, Bo Tang, Qingming Dou, Huashan Zhang, Honghai |
author_facet | Yang, Xiufeng Sun, Guolei Xia, Tian Cha, Muha Zhang, Lei Pang, Bo Tang, Qingming Dou, Huashan Zhang, Honghai |
author_sort | Yang, Xiufeng |
collection | PubMed |
description | Vulpesare widely distributed throughout the world and have undergone drastic physiological and phenotypic changes in response to their environment. However, little is known about the underlying genetic causes of these traits, especially Vulpes corsac. In this study, RNA‐Seq was used to obtain a comprehensive dataset for multiple pooled tissues of corsac fox, and selection analysis of orthologous genes was performed to identify the genes that may be influenced by the low‐temperature environment. More than 6.32 Gb clean reads were obtained and assembled into a total of 173,353 unigenes with an average length of 557 bp for corsac fox. Selective pressure analysis showed that 16 positively selected genes (PSGs) were identified in corsac fox, red fox, and arctic fox. Enrichment analysis of PSGs showed that the LRP11 gene was enriched in several pathways related to the low‐temperature response and might play a key role in response to environmental stimuli of foxes. In addition, several positively selected genes were related to DNA damage repair (ELP2 and CHAF1A), innate immunity (ARRDC4 and S100A12), and the respiratory chain (NDUFA5), and these positively selected genes might play a role in adaptation to harsh wild fox environments. The results of common orthologous gene analysis showed that gene flow or convergent evolution might be an important factor in promoting regional differentiation of foxes. Our study provides a valuable transcriptomic resource for the evolutionary history of the corsac fox and the adaptations to the extreme environments. |
format | Online Article Text |
id | pubmed-9019142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90191422022-04-21 Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) Yang, Xiufeng Sun, Guolei Xia, Tian Cha, Muha Zhang, Lei Pang, Bo Tang, Qingming Dou, Huashan Zhang, Honghai Ecol Evol Research Articles Vulpesare widely distributed throughout the world and have undergone drastic physiological and phenotypic changes in response to their environment. However, little is known about the underlying genetic causes of these traits, especially Vulpes corsac. In this study, RNA‐Seq was used to obtain a comprehensive dataset for multiple pooled tissues of corsac fox, and selection analysis of orthologous genes was performed to identify the genes that may be influenced by the low‐temperature environment. More than 6.32 Gb clean reads were obtained and assembled into a total of 173,353 unigenes with an average length of 557 bp for corsac fox. Selective pressure analysis showed that 16 positively selected genes (PSGs) were identified in corsac fox, red fox, and arctic fox. Enrichment analysis of PSGs showed that the LRP11 gene was enriched in several pathways related to the low‐temperature response and might play a key role in response to environmental stimuli of foxes. In addition, several positively selected genes were related to DNA damage repair (ELP2 and CHAF1A), innate immunity (ARRDC4 and S100A12), and the respiratory chain (NDUFA5), and these positively selected genes might play a role in adaptation to harsh wild fox environments. The results of common orthologous gene analysis showed that gene flow or convergent evolution might be an important factor in promoting regional differentiation of foxes. Our study provides a valuable transcriptomic resource for the evolutionary history of the corsac fox and the adaptations to the extreme environments. John Wiley and Sons Inc. 2022-04-19 /pmc/articles/PMC9019142/ /pubmed/35462974 http://dx.doi.org/10.1002/ece3.8866 Text en © 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Yang, Xiufeng Sun, Guolei Xia, Tian Cha, Muha Zhang, Lei Pang, Bo Tang, Qingming Dou, Huashan Zhang, Honghai Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title | Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title_full | Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title_fullStr | Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title_full_unstemmed | Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title_short | Transcriptome analysis provides new insights into cold adaptation of corsac fox (Vulpes Corsac) |
title_sort | transcriptome analysis provides new insights into cold adaptation of corsac fox (vulpes corsac) |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019142/ https://www.ncbi.nlm.nih.gov/pubmed/35462974 http://dx.doi.org/10.1002/ece3.8866 |
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