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Selection on embryonic haemoglobin in an elevational generalist songbird
Animals developing at high elevation experience a suite of environmental challenges, most notably the low partial pressure of oxygen (PO(2)) in ambient air. In low PO(2), bird species with high-elevation ancestry consistently demonstrate higher hatching success than lowland counterparts, suggesting...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554719/ http://dx.doi.org/10.1098/rsbl.2022.0105 |
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author | Beckman, Elizabeth J. Vargas Campos, Walter Benham, Phred M. Schmitt, C. Jonathan Cheviron, Zachary A. Witt, Christopher C. |
author_facet | Beckman, Elizabeth J. Vargas Campos, Walter Benham, Phred M. Schmitt, C. Jonathan Cheviron, Zachary A. Witt, Christopher C. |
author_sort | Beckman, Elizabeth J. |
collection | PubMed |
description | Animals developing at high elevation experience a suite of environmental challenges, most notably the low partial pressure of oxygen (PO(2)) in ambient air. In low PO(2), bird species with high-elevation ancestry consistently demonstrate higher hatching success than lowland counterparts, suggesting highland birds are adapted to restricted O(2) (hypoxia) in early development. Haemoglobin (Hb), the critical oxygen-transport protein, is a likely target of PO(2)-related selection across ontogeny since Hb isoforms expressed at distinct developmental stages demonstrate different O(2) affinities. To test if Hb function is under PO(2)-related selection at different ontogenetic stages, we sampled a songbird, the hooded siskin (Spinus magellanicus), across two approximately 4000 m elevational transects. We sequenced all of the loci that encode avian Hb isoforms, and tested for signatures of spatially varying selection by comparing divergence patterns in Hb loci to other loci sampled across the genome. We found strong signatures of diversifying selection at non-synonymous sites in loci that contribute to embryonic (α(π), β(H)) and definitive (β(A)) Hb isoforms. This is the first evidence for selection on embryonic haemoglobin in high-elevation Neoaves. We conclude that selection on Hb function at brief, but critical stages of ontogeny may be a vital component to high elevation adaptation in birds. |
format | Online Article Text |
id | pubmed-9554719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95547192022-10-26 Selection on embryonic haemoglobin in an elevational generalist songbird Beckman, Elizabeth J. Vargas Campos, Walter Benham, Phred M. Schmitt, C. Jonathan Cheviron, Zachary A. Witt, Christopher C. Biol Lett Evolutionary Biology Animals developing at high elevation experience a suite of environmental challenges, most notably the low partial pressure of oxygen (PO(2)) in ambient air. In low PO(2), bird species with high-elevation ancestry consistently demonstrate higher hatching success than lowland counterparts, suggesting highland birds are adapted to restricted O(2) (hypoxia) in early development. Haemoglobin (Hb), the critical oxygen-transport protein, is a likely target of PO(2)-related selection across ontogeny since Hb isoforms expressed at distinct developmental stages demonstrate different O(2) affinities. To test if Hb function is under PO(2)-related selection at different ontogenetic stages, we sampled a songbird, the hooded siskin (Spinus magellanicus), across two approximately 4000 m elevational transects. We sequenced all of the loci that encode avian Hb isoforms, and tested for signatures of spatially varying selection by comparing divergence patterns in Hb loci to other loci sampled across the genome. We found strong signatures of diversifying selection at non-synonymous sites in loci that contribute to embryonic (α(π), β(H)) and definitive (β(A)) Hb isoforms. This is the first evidence for selection on embryonic haemoglobin in high-elevation Neoaves. We conclude that selection on Hb function at brief, but critical stages of ontogeny may be a vital component to high elevation adaptation in birds. The Royal Society 2022-10-12 /pmc/articles/PMC9554719/ http://dx.doi.org/10.1098/rsbl.2022.0105 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolutionary Biology Beckman, Elizabeth J. Vargas Campos, Walter Benham, Phred M. Schmitt, C. Jonathan Cheviron, Zachary A. Witt, Christopher C. Selection on embryonic haemoglobin in an elevational generalist songbird |
title | Selection on embryonic haemoglobin in an elevational generalist songbird |
title_full | Selection on embryonic haemoglobin in an elevational generalist songbird |
title_fullStr | Selection on embryonic haemoglobin in an elevational generalist songbird |
title_full_unstemmed | Selection on embryonic haemoglobin in an elevational generalist songbird |
title_short | Selection on embryonic haemoglobin in an elevational generalist songbird |
title_sort | selection on embryonic haemoglobin in an elevational generalist songbird |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554719/ http://dx.doi.org/10.1098/rsbl.2022.0105 |
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