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Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation

The sensory epithelium of the inner ear, found in all extant lineages of vertebrates, has been subjected to over 500 million years of evolution, resulting in the complex inner ear of modern vertebrates. Inner-ear adaptations are as diverse as the species in which they are found, and such unique anat...

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Autores principales: Nisler, Collin R, Narui, Yoshie, Scheib, Emily, Choudhary, Deepanshu, Bowman, Jacob D, Mandayam Bharathi, Harsha, Lynch, Vincent J, Sotomayor, Marcos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089651/
https://www.ncbi.nlm.nih.gov/pubmed/36911992
http://dx.doi.org/10.1093/molbev/msad057
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author Nisler, Collin R
Narui, Yoshie
Scheib, Emily
Choudhary, Deepanshu
Bowman, Jacob D
Mandayam Bharathi, Harsha
Lynch, Vincent J
Sotomayor, Marcos
author_facet Nisler, Collin R
Narui, Yoshie
Scheib, Emily
Choudhary, Deepanshu
Bowman, Jacob D
Mandayam Bharathi, Harsha
Lynch, Vincent J
Sotomayor, Marcos
author_sort Nisler, Collin R
collection PubMed
description The sensory epithelium of the inner ear, found in all extant lineages of vertebrates, has been subjected to over 500 million years of evolution, resulting in the complex inner ear of modern vertebrates. Inner-ear adaptations are as diverse as the species in which they are found, and such unique anatomical variations have been well studied. However, the evolutionary details of the molecular machinery that is required for hearing are less well known. Two molecules that are essential for hearing in vertebrates are cadherin-23 and protocadherin-15, proteins whose interaction with one another acts as the focal point of force transmission when converting sound waves into electrical signals that the brain can interpret. This "tip-link" interaction exists in every lineage of vertebrates, but little is known about the structure or mechanical properties of these proteins in most non-mammalian lineages. Here, we use various techniques to characterize the evolution of this protein interaction. Results show how evolutionary sequence changes in this complex affect its biophysical properties both in simulations and experiments, with variations in interaction strength and dynamics among extant vertebrate lineages. Evolutionary simulations also characterize how the biophysical properties of the complex in turn constrain its evolution and provide a possible explanation for the increase in deafness-causing mutants observed in cadherin-23 relative to protocadherin-15. Together, these results suggest a general picture of tip-link evolution in which selection acted to modify the tip-link interface, although subsequent neutral evolution combined with varying degrees of purifying selection drove additional diversification in modern tetrapods.
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spelling pubmed-100896512023-04-12 Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation Nisler, Collin R Narui, Yoshie Scheib, Emily Choudhary, Deepanshu Bowman, Jacob D Mandayam Bharathi, Harsha Lynch, Vincent J Sotomayor, Marcos Mol Biol Evol Discoveries The sensory epithelium of the inner ear, found in all extant lineages of vertebrates, has been subjected to over 500 million years of evolution, resulting in the complex inner ear of modern vertebrates. Inner-ear adaptations are as diverse as the species in which they are found, and such unique anatomical variations have been well studied. However, the evolutionary details of the molecular machinery that is required for hearing are less well known. Two molecules that are essential for hearing in vertebrates are cadherin-23 and protocadherin-15, proteins whose interaction with one another acts as the focal point of force transmission when converting sound waves into electrical signals that the brain can interpret. This "tip-link" interaction exists in every lineage of vertebrates, but little is known about the structure or mechanical properties of these proteins in most non-mammalian lineages. Here, we use various techniques to characterize the evolution of this protein interaction. Results show how evolutionary sequence changes in this complex affect its biophysical properties both in simulations and experiments, with variations in interaction strength and dynamics among extant vertebrate lineages. Evolutionary simulations also characterize how the biophysical properties of the complex in turn constrain its evolution and provide a possible explanation for the increase in deafness-causing mutants observed in cadherin-23 relative to protocadherin-15. Together, these results suggest a general picture of tip-link evolution in which selection acted to modify the tip-link interface, although subsequent neutral evolution combined with varying degrees of purifying selection drove additional diversification in modern tetrapods. Oxford University Press 2023-03-13 /pmc/articles/PMC10089651/ /pubmed/36911992 http://dx.doi.org/10.1093/molbev/msad057 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Nisler, Collin R
Narui, Yoshie
Scheib, Emily
Choudhary, Deepanshu
Bowman, Jacob D
Mandayam Bharathi, Harsha
Lynch, Vincent J
Sotomayor, Marcos
Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title_full Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title_fullStr Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title_full_unstemmed Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title_short Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation
title_sort interpreting the evolutionary echoes of a protein complex essential for inner-ear mechanosensation
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089651/
https://www.ncbi.nlm.nih.gov/pubmed/36911992
http://dx.doi.org/10.1093/molbev/msad057
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