The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates

Abstract Background The harsh conditions of high-altitude environments are known to drive the evolution of physiological and morphological traits in endothermic animals. These conditions are expected to result in the adaptive evolution of protein coding genes encoded in mitochondrial genomes that ar...

Full description

Bibliographic Details
Published in:BMC Genomics
Main Authors: Edgar G. Gutiérrez, Jorge Ortega, Avery Savoie, J. Antonio Baeza
Format: Article
Language:English
Published: BMC 2023-09-01
Subjects:
Online Access:https://doi.org/10.1186/s12864-023-09596-8
_version_ 1850475334045007872
author Edgar G. Gutiérrez
Jorge Ortega
Avery Savoie
J. Antonio Baeza
author_facet Edgar G. Gutiérrez
Jorge Ortega
Avery Savoie
J. Antonio Baeza
author_sort Edgar G. Gutiérrez
collection DOAJ
container_title BMC Genomics
description Abstract Background The harsh conditions of high-altitude environments are known to drive the evolution of physiological and morphological traits in endothermic animals. These conditions are expected to result in the adaptive evolution of protein coding genes encoded in mitochondrial genomes that are vital for the oxidative phosphorylation pathway. In this study, we formally tested for signatures of adaptive evolution on mitochondrial protein coding genes in Tapirus pinchaque and other odd-toed ungulates inhabiting high-elevation environments. Results The AT-rich mitochondrial genome of T. pinchaque is 16,750 bp long. A phylomitogenomic analysis supports the monophyly of the genus Tapirus and families in the Perissodactyla. The ratio of non-synonymous to synonymous substitutions demonstrated that all mitochondrial genes undergo purifying selection in T. pinchaque and other odd ungulates living at high elevations. Over this negative background selection, Branch Models suggested that cox3 and nad6 might be undergoing stronger purifying selection than other mitochondrial protein coding genes. Furthermore, Site Models suggested that one and four sites in nad2 and nad5, respectively, could be experiencing positive selection. However, these results were supported by Likelihood Ratio Tests but not Bayesian Empirical Bayes posterior probabilities. Additional analyses (in DataMonkey) indicated a relaxation of selection strength in nad6, evidence of episodic diversifying selection in cob, and revealed episodic positive/diversifying selection signatures for two sites in nad1, and one site each in nad2 and nad4. Conclusion The mitochondrial genome of T. pinchaque is an important genomic resource for conservation of this species and this study contributes to the understanding of adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates inhabiting high-altitude environments.
format Article
id doaj-art-4e215eade4694e83aa764a7b7cdb26c9
institution Directory of Open Access Journals
issn 1471-2164
language English
publishDate 2023-09-01
publisher BMC
record_format Article
spelling doaj-art-4e215eade4694e83aa764a7b7cdb26c92025-08-19T22:40:03ZengBMCBMC Genomics1471-21642023-09-0124112110.1186/s12864-023-09596-8The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulatesEdgar G. Gutiérrez0Jorge Ortega1Avery Savoie2J. Antonio Baeza3Laboratorio de Bioconservación y Manejo, Posgrado en Ciencias Químicobiológicas, Departamento de Zoología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación Carpio y Plan de Ayala S/NLaboratorio de Bioconservación y Manejo, Posgrado en Ciencias Químicobiológicas, Departamento de Zoología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación Carpio y Plan de Ayala S/NDepartment of Biological Sciences, 132 Long Hall, Clemson UniversityDepartment of Biological Sciences, 132 Long Hall, Clemson UniversityAbstract Background The harsh conditions of high-altitude environments are known to drive the evolution of physiological and morphological traits in endothermic animals. These conditions are expected to result in the adaptive evolution of protein coding genes encoded in mitochondrial genomes that are vital for the oxidative phosphorylation pathway. In this study, we formally tested for signatures of adaptive evolution on mitochondrial protein coding genes in Tapirus pinchaque and other odd-toed ungulates inhabiting high-elevation environments. Results The AT-rich mitochondrial genome of T. pinchaque is 16,750 bp long. A phylomitogenomic analysis supports the monophyly of the genus Tapirus and families in the Perissodactyla. The ratio of non-synonymous to synonymous substitutions demonstrated that all mitochondrial genes undergo purifying selection in T. pinchaque and other odd ungulates living at high elevations. Over this negative background selection, Branch Models suggested that cox3 and nad6 might be undergoing stronger purifying selection than other mitochondrial protein coding genes. Furthermore, Site Models suggested that one and four sites in nad2 and nad5, respectively, could be experiencing positive selection. However, these results were supported by Likelihood Ratio Tests but not Bayesian Empirical Bayes posterior probabilities. Additional analyses (in DataMonkey) indicated a relaxation of selection strength in nad6, evidence of episodic diversifying selection in cob, and revealed episodic positive/diversifying selection signatures for two sites in nad1, and one site each in nad2 and nad4. Conclusion The mitochondrial genome of T. pinchaque is an important genomic resource for conservation of this species and this study contributes to the understanding of adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates inhabiting high-altitude environments.https://doi.org/10.1186/s12864-023-09596-8Adaptive evolutionMitochondrial genesOdd-toed ungulatesSelectionSelective pressureTapirus pinchaque
spellingShingle Edgar G. Gutiérrez
Jorge Ortega
Avery Savoie
J. Antonio Baeza
The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
Adaptive evolution
Mitochondrial genes
Odd-toed ungulates
Selection
Selective pressure
Tapirus pinchaque
title The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
title_full The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
title_fullStr The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
title_full_unstemmed The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
title_short The mitochondrial genome of the mountain wooly tapir, Tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd-toed ungulates
title_sort mitochondrial genome of the mountain wooly tapir tapirus pinchaque and a formal test of the effect of altitude on the adaptive evolution of mitochondrial protein coding genes in odd toed ungulates
topic Adaptive evolution
Mitochondrial genes
Odd-toed ungulates
Selection
Selective pressure
Tapirus pinchaque
url https://doi.org/10.1186/s12864-023-09596-8
work_keys_str_mv AT edgarggutierrez themitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT jorgeortega themitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT averysavoie themitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT jantoniobaeza themitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT edgarggutierrez mitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT jorgeortega mitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT averysavoie mitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates
AT jantoniobaeza mitochondrialgenomeofthemountainwoolytapirtapiruspinchaqueandaformaltestoftheeffectofaltitudeontheadaptiveevolutionofmitochondrialproteincodinggenesinoddtoedungulates