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Evolution of an extreme hemoglobin phenotype contributed to the sub-Arctic specialization of extinct Steller’s sea cows

View ORCID ProfileAnthony V. Signore, Phillip R. Morrison, Colin J. Brauner, Angela Fago, Roy E. Weber, Kevin L. Campbell
doi: https://doi.org/10.1101/2022.08.29.505768
Anthony V. Signore
1Department of Biological Sciences, University of Manitoba, Winnipeg, R3T 3N2, Canada
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Phillip R. Morrison
2Department of Zoology, University of British Columbia, Vancouver, V6T 1Z4, Canada
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Colin J. Brauner
2Department of Zoology, University of British Columbia, Vancouver, V6T 1Z4, Canada
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Angela Fago
3Department of Biology, Zoophysiology, Aarhus University, DK-8000 Aarhus, Denmark
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Roy E. Weber
3Department of Biology, Zoophysiology, Aarhus University, DK-8000 Aarhus, Denmark
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Kevin L. Campbell
1Department of Biological Sciences, University of Manitoba, Winnipeg, R3T 3N2, Canada
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  • For correspondence: [email protected]
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Abstract

The extinct Steller’s sea cow (Hydrodamalis gigas; †1768) was a whale-sized marine mammal that manifested profound morphological specializations to exploit the harsh coastal climate of the North Pacific. Yet despite first-hand accounts of their biology, little is known regarding the physiological adjustments underlying their evolution to this environment. Here, the adult-expressed hemoglobin (Hb; α2β/δ2) of this sirenian is shown to harbor a fixed amino acid replacement at an otherwise invariant position (β/δ82Lys→Asn) that alters multiple aspects of Hb function. First, our functional characterization of recombinant sirenian Hb proteins demonstrate that the Hb–O2 affinity of this sub-Arctic species was less affected by temperature than those of living (sub)tropical sea cows. This phenotype presumably safeguarded O2 delivery to cool peripheral tissues and largely arises from a reduced intrinsic temperature sensitivity of the H. gigas protein. Additional experiments on H. gigas β/δ82Asn→Lys mutant Hb further reveal this exchange renders Steller’s sea cow Hb unresponsive to the potent intraerythrocytic allosteric effector 2,3-diphosphoglycerate, a radical modification that is the first documented example of this phenotype among mammals. Notably, β/δ82Lys→Asn moreover underlies the secondary evolution of a reduced blood–O2 affinity phenotype that would have promoted heightened tissue and maternal/fetal O2 delivery. This conclusion is bolstered by analyses of two Steller’s sea cow prenatal Hb proteins (Hb Gower I; ζ2ε2 and HbF; α2γ2) that suggest an exclusive embryonic stage expression pattern, and reveal uncommon replacements in H. gigas HbF (γ38Thr→Ile and γ101Glu→Asp) that increased Hb–O2 affinity relative to dugong HbF. Finally, the β/δ82Lys→Asn replacement of the adult/fetal protein is shown to increase protein solubility, which may have elevated red blood cell Hb content within both the adult and fetal circulations and contributed to meeting the elevated metabolic (thermoregulatory) requirements and fetal growth rates associated with this species cold adaptation.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Competing interests: Authors declare that they have no competing interests.

  • Manuscript had been revised to improve the clarity and presentation of the results.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted April 26, 2023.
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Evolution of an extreme hemoglobin phenotype contributed to the sub-Arctic specialization of extinct Steller’s sea cows
Anthony V. Signore, Phillip R. Morrison, Colin J. Brauner, Angela Fago, Roy E. Weber, Kevin L. Campbell
bioRxiv 2022.08.29.505768; doi: https://doi.org/10.1101/2022.08.29.505768
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Evolution of an extreme hemoglobin phenotype contributed to the sub-Arctic specialization of extinct Steller’s sea cows
Anthony V. Signore, Phillip R. Morrison, Colin J. Brauner, Angela Fago, Roy E. Weber, Kevin L. Campbell
bioRxiv 2022.08.29.505768; doi: https://doi.org/10.1101/2022.08.29.505768

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