Current Biology
Volume 33, Issue 1, 9 January 2023, Pages 98-108.e4
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Article
Evolution and molecular basis of a novel allosteric property of crocodilian hemoglobin

https://doi.org/10.1016/j.cub.2022.11.049Get rights and content
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open access

Highlights

  • Crocodilians evolved a unique mode of allosterically regulating hemoglobin function

  • Gain of new function and loss of ancestral function were not mechanistically coupled

  • Gain of novel protein function evolved via numerous substitutions at disparate sites

  • Many of the causative substitutions have highly indirect, context-dependent effects

Summary

The extraordinary breath-hold diving capacity of crocodilians has been ascribed to a unique mode of allosterically regulating hemoglobin (Hb)-oxygenation in circulating red blood cells. We investigated the origin and mechanistic basis of this novel biochemical phenomenon by performing directed mutagenesis experiments on resurrected ancestral Hbs. Comparisons of Hb function between the common ancestor of archosaurs (the group that includes crocodilians and birds) and the last common ancestor of modern crocodilians revealed that regulation of Hb-O2 affinity via allosteric binding of bicarbonate ions represents a croc-specific innovation that evolved in combination with the loss of allosteric regulation by ATP binding. Mutagenesis experiments revealed that evolution of the novel allosteric function in crocodilians and the concomitant loss of ancestral function were not mechanistically coupled and were caused by different sets of substitutions. The gain of bicarbonate sensitivity in crocodilian Hb involved the direct effect of few amino acid substitutions at key sites in combination with indirect effects of numerous other substitutions at structurally disparate sites. Such indirect interaction effects suggest that evolution of the novel protein function was conditional on neutral mutations that produced no adaptive benefit when they first arose but that contributed to a permissive background for subsequent function-altering mutations at other sites. Due to the context dependence of causative substitutions, the unique allosteric properties of crocodilian Hb cannot be easily transplanted into divergent homologs of other species.

Keywords

allostery
ancestral reconstruction
ancestral protein resurrection
biochemical adaptation
hemoglobin
protein evolution
archosaur
epistasis
positive selection
physiological evolution

Data and code availability

  • All reconstructed sequences that we used for ancestral protein resurrection were deposited in GenBank (ON959522-ON959565) and are publicly available as of the date of publication.

  • This paper does not report original code.

  • Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

Cited by (0)

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Present address: Department of Biological Sciences, University of Manitoba, Winnipeg, MB R3T 2N2, Canada

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Lead contact