التفاصيل البيبلوغرافية
| العنوان: |
Evolution of an extreme hemoglobin phenotype contributed to the sub-Arctic specialization of extinct Steller's sea cows |
| المؤلفون: |
Signori, Anthony V., Morrison, Philip R., Brauner, Colin J., Fago, Angela, Weber, Roy E., Campbell, Kevin L. |
| المصدر: |
Signori , A V , Morrison , P R , Brauner , C J , Fago , A , Weber , R E & Campbell , K L 2023 , ' Evolution of an extreme hemoglobin phenotype contributed to the sub-Arctic specialization of extinct Steller's sea cows ' , eLife , vol. 12 , e85414 . https://doi.org/10.7554/eLife.85414 |
| سنة النشر: |
2023 |
| مصطلحات موضوعية: |
Animals, Climate, Dugong, Hemoglobins/genetics, Mammals, Oxygen, envir |
| الوصف: |
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; α 2 β/δ 2 ) 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 demonstrates that the Hb-O 2 affinity of this sub-Arctic species was less affected by temperature than those of living (sub)tropical sea cows. This phenotype presumably safeguarded O 2 delivery to cool periph-eral 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-O 2 affinity phenotype that would have promoted heightened tissue and maternal/ fetal O 2 delivery. This conclusion is bolstered by analyses of two Steller’s sea cow prenatal Hb proteins (Hb Gower I; ζ 2 ε 2 and HbF; α 2 γ 2 ) that suggest an exclusive embryonic stage expression pattern, and reveal uncommon replacements in H. gigas HbF (γ38Thr→Ile and γ101Glu→Asp) that increased Hb-O 2 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) . |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
English |
| Relation: |
https://pure.au.dk/portal/en/publications/d49b3cdd-7881-4150-91af-b5fa592b4002 |
| الاتاحة: |
https://pure.au.dk/portal/en/publications/d49b3cdd-7881-4150-91af-b5fa592b4002 |
| Rights: |
undefined |
| رقم الانضمام: |
edsbas.22EBAB55 |
| قاعدة البيانات: |
BASE |