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Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors
Sensory receptor evolution can imply trade-offs between ligands, but the extent to which such trade-offs occur and the underlying processes shaping their evolution is not well understood. For example, hummingbirds have repurposed their ancestral savory receptor (T1R1–T1R3) to detect sugars, but the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826506/ https://www.ncbi.nlm.nih.gov/pubmed/34978567 http://dx.doi.org/10.1093/molbev/msab367 |
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author | Cockburn, Glenn Ko, Meng-Ching Sadanandan, Keren R Miller, Eliot T Nakagita, Tomoya Monte, Amanda Cho, Sungbo Roura, Eugeni Toda, Yasuka Baldwin, Maude W |
author_facet | Cockburn, Glenn Ko, Meng-Ching Sadanandan, Keren R Miller, Eliot T Nakagita, Tomoya Monte, Amanda Cho, Sungbo Roura, Eugeni Toda, Yasuka Baldwin, Maude W |
author_sort | Cockburn, Glenn |
collection | PubMed |
description | Sensory receptor evolution can imply trade-offs between ligands, but the extent to which such trade-offs occur and the underlying processes shaping their evolution is not well understood. For example, hummingbirds have repurposed their ancestral savory receptor (T1R1–T1R3) to detect sugars, but the impact of this sensory shift on amino acid perception is unclear. Here, we use functional and behavioral approaches to show that the hummingbird T1R1–T1R3 acts as a bifunctional receptor responsive to both sugars and amino acids. Our comparative analyses reveal substantial functional diversity across the hummingbird radiation and suggest an evolutionary timeline for T1R1–T1R3 retuning. Finally, we identify a novel form of synergism between sugars and amino acids in vertebrate taste receptors. This work uncovers an unexplored axis of sensory diversity, suggesting new ways in which nectar chemistry and pollinator preferences can coevolve. |
format | Online Article Text |
id | pubmed-8826506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88265062022-02-09 Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors Cockburn, Glenn Ko, Meng-Ching Sadanandan, Keren R Miller, Eliot T Nakagita, Tomoya Monte, Amanda Cho, Sungbo Roura, Eugeni Toda, Yasuka Baldwin, Maude W Mol Biol Evol Discoveries Sensory receptor evolution can imply trade-offs between ligands, but the extent to which such trade-offs occur and the underlying processes shaping their evolution is not well understood. For example, hummingbirds have repurposed their ancestral savory receptor (T1R1–T1R3) to detect sugars, but the impact of this sensory shift on amino acid perception is unclear. Here, we use functional and behavioral approaches to show that the hummingbird T1R1–T1R3 acts as a bifunctional receptor responsive to both sugars and amino acids. Our comparative analyses reveal substantial functional diversity across the hummingbird radiation and suggest an evolutionary timeline for T1R1–T1R3 retuning. Finally, we identify a novel form of synergism between sugars and amino acids in vertebrate taste receptors. This work uncovers an unexplored axis of sensory diversity, suggesting new ways in which nectar chemistry and pollinator preferences can coevolve. Oxford University Press 2022-01-03 /pmc/articles/PMC8826506/ /pubmed/34978567 http://dx.doi.org/10.1093/molbev/msab367 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Cockburn, Glenn Ko, Meng-Ching Sadanandan, Keren R Miller, Eliot T Nakagita, Tomoya Monte, Amanda Cho, Sungbo Roura, Eugeni Toda, Yasuka Baldwin, Maude W Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title | Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title_full | Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title_fullStr | Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title_full_unstemmed | Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title_short | Synergism, Bifunctionality, and the Evolution of a Gradual Sensory Trade-off in Hummingbird Taste Receptors |
title_sort | synergism, bifunctionality, and the evolution of a gradual sensory trade-off in hummingbird taste receptors |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826506/ https://www.ncbi.nlm.nih.gov/pubmed/34978567 http://dx.doi.org/10.1093/molbev/msab367 |
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