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Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization

Convergent adaptation to the same environment by multiple lineages frequently involves rapid evolutionary change at the same genes, implicating these genes as important for environmental adaptation. Such adaptive molecular changes may yield either change or loss of protein function; loss of function...

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Autores principales: Graham, Allie M, Jamison, Jerrica M, Bustos, Marisol, Cournoyer, Charlotte, Michaels, Alexa, Presnell, Jason S, Richter, Rebecca, Crocker, Daniel E, Fustukjian, Ari, Hunter, Margaret E, Rea, Lorrie D, Marsillach, Judit, Furlong, Clement E, Meyer, Wynn K, Clark, Nathan L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202596/
https://www.ncbi.nlm.nih.gov/pubmed/37146172
http://dx.doi.org/10.1093/molbev/msad104
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author Graham, Allie M
Jamison, Jerrica M
Bustos, Marisol
Cournoyer, Charlotte
Michaels, Alexa
Presnell, Jason S
Richter, Rebecca
Crocker, Daniel E
Fustukjian, Ari
Hunter, Margaret E
Rea, Lorrie D
Marsillach, Judit
Furlong, Clement E
Meyer, Wynn K
Clark, Nathan L
author_facet Graham, Allie M
Jamison, Jerrica M
Bustos, Marisol
Cournoyer, Charlotte
Michaels, Alexa
Presnell, Jason S
Richter, Rebecca
Crocker, Daniel E
Fustukjian, Ari
Hunter, Margaret E
Rea, Lorrie D
Marsillach, Judit
Furlong, Clement E
Meyer, Wynn K
Clark, Nathan L
author_sort Graham, Allie M
collection PubMed
description Convergent adaptation to the same environment by multiple lineages frequently involves rapid evolutionary change at the same genes, implicating these genes as important for environmental adaptation. Such adaptive molecular changes may yield either change or loss of protein function; loss of function can eliminate newly deleterious proteins or reduce energy necessary for protein production. We previously found a striking case of recurrent pseudogenization of the Paraoxonase 1 (Pon1) gene among aquatic mammal lineages—Pon1 became a pseudogene with genetic lesions, such as stop codons and frameshifts, at least four times independently in aquatic and semiaquatic mammals. Here, we assess the landscape and pace of pseudogenization by studying Pon1 sequences, expression levels, and enzymatic activity across four aquatic and semiaquatic mammal lineages: pinnipeds, cetaceans, otters, and beavers. We observe in beavers and pinnipeds an unexpected reduction in expression of Pon3, a paralog with similar expression patterns but different substrate preferences. Ultimately, in all lineages with aquatic/semiaquatic members, we find that preceding any coding-level pseudogenization events in Pon1, there is a drastic decrease in expression, followed by relaxed selection, thus allowing accumulation of disrupting mutations. The recurrent loss of Pon1 function in aquatic/semiaquatic lineages is consistent with a benefit to Pon1 functional loss in aquatic environments. Accordingly, we examine diving and dietary traits across pinniped species as potential driving forces of Pon1 functional loss. We find that loss is best associated with diving activity and likely results from changes in selective pressures associated with hypoxia and hypoxia-induced inflammation.
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spelling pubmed-102025962023-05-23 Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization Graham, Allie M Jamison, Jerrica M Bustos, Marisol Cournoyer, Charlotte Michaels, Alexa Presnell, Jason S Richter, Rebecca Crocker, Daniel E Fustukjian, Ari Hunter, Margaret E Rea, Lorrie D Marsillach, Judit Furlong, Clement E Meyer, Wynn K Clark, Nathan L Mol Biol Evol Discoveries Convergent adaptation to the same environment by multiple lineages frequently involves rapid evolutionary change at the same genes, implicating these genes as important for environmental adaptation. Such adaptive molecular changes may yield either change or loss of protein function; loss of function can eliminate newly deleterious proteins or reduce energy necessary for protein production. We previously found a striking case of recurrent pseudogenization of the Paraoxonase 1 (Pon1) gene among aquatic mammal lineages—Pon1 became a pseudogene with genetic lesions, such as stop codons and frameshifts, at least four times independently in aquatic and semiaquatic mammals. Here, we assess the landscape and pace of pseudogenization by studying Pon1 sequences, expression levels, and enzymatic activity across four aquatic and semiaquatic mammal lineages: pinnipeds, cetaceans, otters, and beavers. We observe in beavers and pinnipeds an unexpected reduction in expression of Pon3, a paralog with similar expression patterns but different substrate preferences. Ultimately, in all lineages with aquatic/semiaquatic members, we find that preceding any coding-level pseudogenization events in Pon1, there is a drastic decrease in expression, followed by relaxed selection, thus allowing accumulation of disrupting mutations. The recurrent loss of Pon1 function in aquatic/semiaquatic lineages is consistent with a benefit to Pon1 functional loss in aquatic environments. Accordingly, we examine diving and dietary traits across pinniped species as potential driving forces of Pon1 functional loss. We find that loss is best associated with diving activity and likely results from changes in selective pressures associated with hypoxia and hypoxia-induced inflammation. Oxford University Press 2023-05-05 /pmc/articles/PMC10202596/ /pubmed/37146172 http://dx.doi.org/10.1093/molbev/msad104 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/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
Graham, Allie M
Jamison, Jerrica M
Bustos, Marisol
Cournoyer, Charlotte
Michaels, Alexa
Presnell, Jason S
Richter, Rebecca
Crocker, Daniel E
Fustukjian, Ari
Hunter, Margaret E
Rea, Lorrie D
Marsillach, Judit
Furlong, Clement E
Meyer, Wynn K
Clark, Nathan L
Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title_full Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title_fullStr Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title_full_unstemmed Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title_short Reduction of Paraoxonase Expression Followed by Inactivation across Independent Semiaquatic Mammals Suggests Stepwise Path to Pseudogenization
title_sort reduction of paraoxonase expression followed by inactivation across independent semiaquatic mammals suggests stepwise path to pseudogenization
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202596/
https://www.ncbi.nlm.nih.gov/pubmed/37146172
http://dx.doi.org/10.1093/molbev/msad104
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