Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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
_version_ 1783710762793959424
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
work_keys_str_mv AT wearingoliverh theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT ivycatherinem theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT gutierrezpintonatalia theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT velottajonathanp theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT campbellstatonshanec theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT natarajanchandrasekhar theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT chevironzacharya theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT storzjayf theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT scottgrahamr theadaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT wearingoliverh adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT ivycatherinem adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT gutierrezpintonatalia adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT velottajonathanp adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT campbellstatonshanec adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT natarajanchandrasekhar adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT chevironzacharya adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT storzjayf adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice
AT scottgrahamr adaptivebenefitofevolvedincreasesinhemoglobino2affinityiscontingentontissueo2diffusingcapacityinhighaltitudedeermice