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Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes

SIMPLE SUMMARY: The role of aquaporins (AQPs) in the adaptation of amphibious fishes to terrestrial environments was investigated using genome mining, phylogenetics, molecular evolution, and protein structure modelling. Evidence of adaptive evolution was found in 21 AQPs belonging to 5 different cla...

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Autores principales: Lorente-Martínez, Héctor, Agorreta, Ainhoa, Irisarri, Iker, Zardoya, Rafael, Edwards, Scott V., San Mauro, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295795/
https://www.ncbi.nlm.nih.gov/pubmed/37372131
http://dx.doi.org/10.3390/biology12060846
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author Lorente-Martínez, Héctor
Agorreta, Ainhoa
Irisarri, Iker
Zardoya, Rafael
Edwards, Scott V.
San Mauro, Diego
author_facet Lorente-Martínez, Héctor
Agorreta, Ainhoa
Irisarri, Iker
Zardoya, Rafael
Edwards, Scott V.
San Mauro, Diego
author_sort Lorente-Martínez, Héctor
collection PubMed
description SIMPLE SUMMARY: The role of aquaporins (AQPs) in the adaptation of amphibious fishes to terrestrial environments was investigated using genome mining, phylogenetics, molecular evolution, and protein structure modelling. Evidence of adaptive evolution was found in 21 AQPs belonging to 5 different classes but predominantly to the AQP11 class. These sequence changes indicate that the modifications in molecular function and/or structure could be related to the process of adaptation to an amphibious lifestyle. ABSTRACT: Aquaporins (AQPs) are a highly diverse family of transmembrane proteins involved in osmotic regulation that played an important role in the conquest of land by tetrapods. However, little is known about their possible implication in the acquisition of an amphibious lifestyle in actinopterygian fishes. Herein, we investigated the molecular evolution of AQPs in 22 amphibious actinopterygian fishes by assembling a comprehensive dataset that was used to (1) catalogue AQP paralog members and classes; (2) determine the gene family birth and death process; (3) test for positive selection in a phylogenetic framework; and (4) reconstruct structural protein models. We found evidence of adaptive evolution in 21 AQPs belonging to 5 different classes. Almost half of the tree branches and protein sites that were under positive selection were found in the AQP11 class. The detected sequence changes indicate modifications in molecular function and/or structure, which could be related to adaptation to an amphibious lifestyle. AQP11 orthologues appear to be the most promising candidates to have facilitated the processes of the water-to-land transition in amphibious fishes. Additionally, the signature of positive selection found in the AQP11b stem branch of the Gobiidae clade suggests a possible case of exaptation in this clade.
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spelling pubmed-102957952023-06-28 Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes Lorente-Martínez, Héctor Agorreta, Ainhoa Irisarri, Iker Zardoya, Rafael Edwards, Scott V. San Mauro, Diego Biology (Basel) Article SIMPLE SUMMARY: The role of aquaporins (AQPs) in the adaptation of amphibious fishes to terrestrial environments was investigated using genome mining, phylogenetics, molecular evolution, and protein structure modelling. Evidence of adaptive evolution was found in 21 AQPs belonging to 5 different classes but predominantly to the AQP11 class. These sequence changes indicate that the modifications in molecular function and/or structure could be related to the process of adaptation to an amphibious lifestyle. ABSTRACT: Aquaporins (AQPs) are a highly diverse family of transmembrane proteins involved in osmotic regulation that played an important role in the conquest of land by tetrapods. However, little is known about their possible implication in the acquisition of an amphibious lifestyle in actinopterygian fishes. Herein, we investigated the molecular evolution of AQPs in 22 amphibious actinopterygian fishes by assembling a comprehensive dataset that was used to (1) catalogue AQP paralog members and classes; (2) determine the gene family birth and death process; (3) test for positive selection in a phylogenetic framework; and (4) reconstruct structural protein models. We found evidence of adaptive evolution in 21 AQPs belonging to 5 different classes. Almost half of the tree branches and protein sites that were under positive selection were found in the AQP11 class. The detected sequence changes indicate modifications in molecular function and/or structure, which could be related to adaptation to an amphibious lifestyle. AQP11 orthologues appear to be the most promising candidates to have facilitated the processes of the water-to-land transition in amphibious fishes. Additionally, the signature of positive selection found in the AQP11b stem branch of the Gobiidae clade suggests a possible case of exaptation in this clade. MDPI 2023-06-12 /pmc/articles/PMC10295795/ /pubmed/37372131 http://dx.doi.org/10.3390/biology12060846 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lorente-Martínez, Héctor
Agorreta, Ainhoa
Irisarri, Iker
Zardoya, Rafael
Edwards, Scott V.
San Mauro, Diego
Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title_full Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title_fullStr Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title_full_unstemmed Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title_short Multiple Instances of Adaptive Evolution in Aquaporins of Amphibious Fishes
title_sort multiple instances of adaptive evolution in aquaporins of amphibious fishes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295795/
https://www.ncbi.nlm.nih.gov/pubmed/37372131
http://dx.doi.org/10.3390/biology12060846
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