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High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses

The high‐altitude environment may drive vertebrate evolution in a certain way, and vertebrates living in different altitude environments might have different energy requirements. We hypothesized that the high‐altitude environment might impose different influences on vertebrate mitochondrial genomes...

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Autores principales: Wang, Xibao, Zhou, Shengyang, Wu, Xiaoyang, Wei, Qinguo, Shang, Yongquan, Sun, Guolei, Mei, Xuesong, Dong, Yuehuan, Sha, Weilai, Zhang, Honghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571627/
https://www.ncbi.nlm.nih.gov/pubmed/34765161
http://dx.doi.org/10.1002/ece3.8189
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author Wang, Xibao
Zhou, Shengyang
Wu, Xiaoyang
Wei, Qinguo
Shang, Yongquan
Sun, Guolei
Mei, Xuesong
Dong, Yuehuan
Sha, Weilai
Zhang, Honghai
author_facet Wang, Xibao
Zhou, Shengyang
Wu, Xiaoyang
Wei, Qinguo
Shang, Yongquan
Sun, Guolei
Mei, Xuesong
Dong, Yuehuan
Sha, Weilai
Zhang, Honghai
author_sort Wang, Xibao
collection PubMed
description The high‐altitude environment may drive vertebrate evolution in a certain way, and vertebrates living in different altitude environments might have different energy requirements. We hypothesized that the high‐altitude environment might impose different influences on vertebrate mitochondrial genomes (mtDNA). We used selection pressure analyses and PIC (phylogenetic independent contrasts) analysis to detect the evolutionary rate of vertebrate mtDNA protein‐coding genes (PCGs) from different altitudes. The results showed that the ratio of nonsynonymous/synonymous substitutions (dN/dS) in the mtDNA PCGs was significantly higher in high‐altitude vertebrates than in low‐altitude vertebrates. The seven rapidly evolving genes were shared by the high‐altitude vertebrates, and only one positive selection gene (ND5 gene) was detected in the high‐altitude vertebrates. Our results suggest the mtDNA evolutionary rate in high‐altitude vertebrates was higher than in low‐altitude vertebrates as their evolution requires more energy in a high‐altitude environment. Our study demonstrates the high‐altitude environment (low atmospheric O(2) levels) drives vertebrate evolution in mtDNA PCGs.
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spelling pubmed-85716272021-11-10 High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses Wang, Xibao Zhou, Shengyang Wu, Xiaoyang Wei, Qinguo Shang, Yongquan Sun, Guolei Mei, Xuesong Dong, Yuehuan Sha, Weilai Zhang, Honghai Ecol Evol Research Articles The high‐altitude environment may drive vertebrate evolution in a certain way, and vertebrates living in different altitude environments might have different energy requirements. We hypothesized that the high‐altitude environment might impose different influences on vertebrate mitochondrial genomes (mtDNA). We used selection pressure analyses and PIC (phylogenetic independent contrasts) analysis to detect the evolutionary rate of vertebrate mtDNA protein‐coding genes (PCGs) from different altitudes. The results showed that the ratio of nonsynonymous/synonymous substitutions (dN/dS) in the mtDNA PCGs was significantly higher in high‐altitude vertebrates than in low‐altitude vertebrates. The seven rapidly evolving genes were shared by the high‐altitude vertebrates, and only one positive selection gene (ND5 gene) was detected in the high‐altitude vertebrates. Our results suggest the mtDNA evolutionary rate in high‐altitude vertebrates was higher than in low‐altitude vertebrates as their evolution requires more energy in a high‐altitude environment. Our study demonstrates the high‐altitude environment (low atmospheric O(2) levels) drives vertebrate evolution in mtDNA PCGs. John Wiley and Sons Inc. 2021-10-05 /pmc/articles/PMC8571627/ /pubmed/34765161 http://dx.doi.org/10.1002/ece3.8189 Text en © 2021 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
Wang, Xibao
Zhou, Shengyang
Wu, Xiaoyang
Wei, Qinguo
Shang, Yongquan
Sun, Guolei
Mei, Xuesong
Dong, Yuehuan
Sha, Weilai
Zhang, Honghai
High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title_full High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title_fullStr High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title_full_unstemmed High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title_short High‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
title_sort high‐altitude adaptation in vertebrates as revealed by mitochondrial genome analyses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571627/
https://www.ncbi.nlm.nih.gov/pubmed/34765161
http://dx.doi.org/10.1002/ece3.8189
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