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The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice
BACKGROUND: Complex organismal traits are often the result of multiple interacting genes and sub-organismal phenotypes, but how these interactions shape the evolutionary trajectories of adaptive traits is poorly understood. We examined how functional interactions between cardiorespiratory traits con...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218429/ https://www.ncbi.nlm.nih.gov/pubmed/34158035 http://dx.doi.org/10.1186/s12915-021-01059-4 |
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author | Wearing, Oliver H. Ivy, Catherine M. Gutiérrez-Pinto, Natalia Velotta, Jonathan P. Campbell-Staton, Shane C. Natarajan, Chandrasekhar Cheviron, Zachary A. Storz, Jay F. Scott, Graham R. |
author_facet | Wearing, Oliver H. Ivy, Catherine M. Gutiérrez-Pinto, Natalia Velotta, Jonathan P. Campbell-Staton, Shane C. Natarajan, Chandrasekhar Cheviron, Zachary A. Storz, Jay F. Scott, Graham R. |
author_sort | Wearing, Oliver H. |
collection | PubMed |
description | BACKGROUND: Complex organismal traits are often the result of multiple interacting genes and sub-organismal phenotypes, but how these interactions shape the evolutionary trajectories of adaptive traits is poorly understood. We examined how functional interactions between cardiorespiratory traits contribute to adaptive increases in the capacity for aerobic thermogenesis (maximal O(2) consumption, V̇O(2)max, during acute cold exposure) in high-altitude deer mice (Peromyscus maniculatus). We crossed highland and lowland deer mice to produce F(2) inter-population hybrids, which expressed genetically based variation in hemoglobin (Hb) O(2) affinity on a mixed genetic background. We then combined physiological experiments and mathematical modeling of the O(2) transport pathway to examine the links between cardiorespiratory traits and V̇O(2)max. RESULTS: Physiological experiments revealed that increases in Hb-O(2) affinity of red blood cells improved blood oxygenation in hypoxia but were not associated with an enhancement in V̇O(2)max. Sensitivity analyses performed using mathematical modeling showed that the influence of Hb-O(2) affinity on V̇O(2)max in hypoxia was contingent on the capacity for O(2) diffusion in active tissues. CONCLUSIONS: These results suggest that increases in Hb-O(2) affinity would only have adaptive value in hypoxic conditions if concurrent with or preceded by increases in tissue O(2) diffusing capacity. In high-altitude deer mice, the adaptive benefit of increasing Hb-O(2) affinity is contingent on the capacity to extract O(2) from the blood, which helps resolve controversies about the general role of hemoglobin function in hypoxia tolerance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01059-4. |
format | Online Article Text |
id | pubmed-8218429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82184292021-06-23 The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice Wearing, Oliver H. Ivy, Catherine M. Gutiérrez-Pinto, Natalia Velotta, Jonathan P. Campbell-Staton, Shane C. Natarajan, Chandrasekhar Cheviron, Zachary A. Storz, Jay F. Scott, Graham R. BMC Biol Research Article BACKGROUND: Complex organismal traits are often the result of multiple interacting genes and sub-organismal phenotypes, but how these interactions shape the evolutionary trajectories of adaptive traits is poorly understood. We examined how functional interactions between cardiorespiratory traits contribute to adaptive increases in the capacity for aerobic thermogenesis (maximal O(2) consumption, V̇O(2)max, during acute cold exposure) in high-altitude deer mice (Peromyscus maniculatus). We crossed highland and lowland deer mice to produce F(2) inter-population hybrids, which expressed genetically based variation in hemoglobin (Hb) O(2) affinity on a mixed genetic background. We then combined physiological experiments and mathematical modeling of the O(2) transport pathway to examine the links between cardiorespiratory traits and V̇O(2)max. RESULTS: Physiological experiments revealed that increases in Hb-O(2) affinity of red blood cells improved blood oxygenation in hypoxia but were not associated with an enhancement in V̇O(2)max. Sensitivity analyses performed using mathematical modeling showed that the influence of Hb-O(2) affinity on V̇O(2)max in hypoxia was contingent on the capacity for O(2) diffusion in active tissues. CONCLUSIONS: These results suggest that increases in Hb-O(2) affinity would only have adaptive value in hypoxic conditions if concurrent with or preceded by increases in tissue O(2) diffusing capacity. In high-altitude deer mice, the adaptive benefit of increasing Hb-O(2) affinity is contingent on the capacity to extract O(2) from the blood, which helps resolve controversies about the general role of hemoglobin function in hypoxia tolerance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01059-4. BioMed Central 2021-06-22 /pmc/articles/PMC8218429/ /pubmed/34158035 http://dx.doi.org/10.1186/s12915-021-01059-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Wearing, Oliver H. Ivy, Catherine M. Gutiérrez-Pinto, Natalia Velotta, Jonathan P. Campbell-Staton, Shane C. Natarajan, Chandrasekhar Cheviron, Zachary A. Storz, Jay F. Scott, Graham R. The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title | The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title_full | The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title_fullStr | The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title_full_unstemmed | The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title_short | The adaptive benefit of evolved increases in hemoglobin-O(2) affinity is contingent on tissue O(2) diffusing capacity in high-altitude deer mice |
title_sort | adaptive benefit of evolved increases in hemoglobin-o(2) affinity is contingent on tissue o(2) diffusing capacity in high-altitude deer mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218429/ https://www.ncbi.nlm.nih.gov/pubmed/34158035 http://dx.doi.org/10.1186/s12915-021-01059-4 |
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