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Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors

The expansion and pruning of ion channel families has played a crucial role in the evolution of nervous systems. Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels with distinct roles in synaptic transmission at the neuromuscular junction, the central and peripheral nervous sys...

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Autores principales: Marcovich, Irina, Moglie, Marcelo J, Carpaneto Freixas, Agustín E, Trigila, Anabella P, Franchini, Lucia F, Plazas, Paola V, Lipovsek, Marcela, Elgoyhen, Ana Belén
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086180/
https://www.ncbi.nlm.nih.gov/pubmed/31821508
http://dx.doi.org/10.1093/molbev/msz290
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author Marcovich, Irina
Moglie, Marcelo J
Carpaneto Freixas, Agustín E
Trigila, Anabella P
Franchini, Lucia F
Plazas, Paola V
Lipovsek, Marcela
Elgoyhen, Ana Belén
author_facet Marcovich, Irina
Moglie, Marcelo J
Carpaneto Freixas, Agustín E
Trigila, Anabella P
Franchini, Lucia F
Plazas, Paola V
Lipovsek, Marcela
Elgoyhen, Ana Belén
author_sort Marcovich, Irina
collection PubMed
description The expansion and pruning of ion channel families has played a crucial role in the evolution of nervous systems. Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels with distinct roles in synaptic transmission at the neuromuscular junction, the central and peripheral nervous system, and the inner ear. Remarkably, the complement of nAChR subunits has been highly conserved along vertebrate phylogeny. To ask whether the different subtypes of receptors underwent different evolutionary trajectories, we performed a comprehensive analysis of vertebrate nAChRs coding sequences, mouse single-cell expression patterns, and comparative functional properties of receptors from three representative tetrapod species. We found significant differences between hair cell and neuronal receptors that were most likely shaped by the differences in coexpression patterns and coassembly rules of component subunits. Thus, neuronal nAChRs showed high degree of coding sequence conservation, coupled to greater coexpression variance and conservation of functional properties across tetrapod clades. In contrast, hair cell α9α10 nAChRs exhibited greater sequence divergence, narrow coexpression pattern, and great variability of functional properties across species. These results point to differential substrates for random change within the family of gene paralogs that relate to the segregated roles of nAChRs in synaptic transmission.
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spelling pubmed-70861802020-03-26 Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors Marcovich, Irina Moglie, Marcelo J Carpaneto Freixas, Agustín E Trigila, Anabella P Franchini, Lucia F Plazas, Paola V Lipovsek, Marcela Elgoyhen, Ana Belén Mol Biol Evol Discoveries The expansion and pruning of ion channel families has played a crucial role in the evolution of nervous systems. Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels with distinct roles in synaptic transmission at the neuromuscular junction, the central and peripheral nervous system, and the inner ear. Remarkably, the complement of nAChR subunits has been highly conserved along vertebrate phylogeny. To ask whether the different subtypes of receptors underwent different evolutionary trajectories, we performed a comprehensive analysis of vertebrate nAChRs coding sequences, mouse single-cell expression patterns, and comparative functional properties of receptors from three representative tetrapod species. We found significant differences between hair cell and neuronal receptors that were most likely shaped by the differences in coexpression patterns and coassembly rules of component subunits. Thus, neuronal nAChRs showed high degree of coding sequence conservation, coupled to greater coexpression variance and conservation of functional properties across tetrapod clades. In contrast, hair cell α9α10 nAChRs exhibited greater sequence divergence, narrow coexpression pattern, and great variability of functional properties across species. These results point to differential substrates for random change within the family of gene paralogs that relate to the segregated roles of nAChRs in synaptic transmission. Oxford University Press 2020-04 2019-12-10 /pmc/articles/PMC7086180/ /pubmed/31821508 http://dx.doi.org/10.1093/molbev/msz290 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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
Marcovich, Irina
Moglie, Marcelo J
Carpaneto Freixas, Agustín E
Trigila, Anabella P
Franchini, Lucia F
Plazas, Paola V
Lipovsek, Marcela
Elgoyhen, Ana Belén
Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title_full Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title_fullStr Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title_full_unstemmed Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title_short Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
title_sort distinct evolutionary trajectories of neuronal and hair cell nicotinic acetylcholine receptors
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086180/
https://www.ncbi.nlm.nih.gov/pubmed/31821508
http://dx.doi.org/10.1093/molbev/msz290
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