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Diet and the evolution of ADH7 across seven orders of mammals

Dietary variation within and across species drives the eco-evolutionary responsiveness of genes necessary to metabolize nutrients and other components. Recent evidence from humans and other mammals suggests that sugar-rich diets of floral nectar and ripe fruit have favoured mutations in, and functio...

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Autores principales: Pinto, Swellan L., Janiak, Mareike C., Dutyschaever, Gwen, Barros, Marília A. S., Chavarria, Adrian Guadamuz, Martin, Maria Pia, Tuh, Fred Y. Y., Valverde, Carmen Soto, Sims, Lisa M., Barclay, Robert M. R., Wells, Konstans, Dominy, Nathaniel J., Pessoa, Daniel M. A., Carrigan, Matthew A., Melin, Amanda D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336374/
https://www.ncbi.nlm.nih.gov/pubmed/37448478
http://dx.doi.org/10.1098/rsos.230451
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author Pinto, Swellan L.
Janiak, Mareike C.
Dutyschaever, Gwen
Barros, Marília A. S.
Chavarria, Adrian Guadamuz
Martin, Maria Pia
Tuh, Fred Y. Y.
Valverde, Carmen Soto
Sims, Lisa M.
Barclay, Robert M. R.
Wells, Konstans
Dominy, Nathaniel J.
Pessoa, Daniel M. A.
Carrigan, Matthew A.
Melin, Amanda D.
author_facet Pinto, Swellan L.
Janiak, Mareike C.
Dutyschaever, Gwen
Barros, Marília A. S.
Chavarria, Adrian Guadamuz
Martin, Maria Pia
Tuh, Fred Y. Y.
Valverde, Carmen Soto
Sims, Lisa M.
Barclay, Robert M. R.
Wells, Konstans
Dominy, Nathaniel J.
Pessoa, Daniel M. A.
Carrigan, Matthew A.
Melin, Amanda D.
author_sort Pinto, Swellan L.
collection PubMed
description Dietary variation within and across species drives the eco-evolutionary responsiveness of genes necessary to metabolize nutrients and other components. Recent evidence from humans and other mammals suggests that sugar-rich diets of floral nectar and ripe fruit have favoured mutations in, and functional preservation of, the ADH7 gene, which encodes the ADH class 4 enzyme responsible for metabolizing ethanol. Here we interrogate a large, comparative dataset of ADH7 gene sequence variation, including that underlying the amino acid residue located at the key site (294) that regulates the affinity of ADH7 for ethanol. Our analyses span 171 mammal species, including 59 newly sequenced. We report extensive variation, especially among frugivorous and nectarivorous bats, with potential for functional impact. We also report widespread variation in the retention and probable pseudogenization of ADH7. However, we find little statistical evidence of an overarching impact of dietary behaviour on putative ADH7 function or presence of derived alleles at site 294 across mammals, which suggests that the evolution of ADH7 is shaped by complex factors. Our study reports extensive new diversity in a gene of longstanding ecological interest, offers new sources of variation to be explored in functional assays in future study, and advances our understanding of the processes of molecular evolution.
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spelling pubmed-103363742023-07-13 Diet and the evolution of ADH7 across seven orders of mammals Pinto, Swellan L. Janiak, Mareike C. Dutyschaever, Gwen Barros, Marília A. S. Chavarria, Adrian Guadamuz Martin, Maria Pia Tuh, Fred Y. Y. Valverde, Carmen Soto Sims, Lisa M. Barclay, Robert M. R. Wells, Konstans Dominy, Nathaniel J. Pessoa, Daniel M. A. Carrigan, Matthew A. Melin, Amanda D. R Soc Open Sci Genetics and Genomics Dietary variation within and across species drives the eco-evolutionary responsiveness of genes necessary to metabolize nutrients and other components. Recent evidence from humans and other mammals suggests that sugar-rich diets of floral nectar and ripe fruit have favoured mutations in, and functional preservation of, the ADH7 gene, which encodes the ADH class 4 enzyme responsible for metabolizing ethanol. Here we interrogate a large, comparative dataset of ADH7 gene sequence variation, including that underlying the amino acid residue located at the key site (294) that regulates the affinity of ADH7 for ethanol. Our analyses span 171 mammal species, including 59 newly sequenced. We report extensive variation, especially among frugivorous and nectarivorous bats, with potential for functional impact. We also report widespread variation in the retention and probable pseudogenization of ADH7. However, we find little statistical evidence of an overarching impact of dietary behaviour on putative ADH7 function or presence of derived alleles at site 294 across mammals, which suggests that the evolution of ADH7 is shaped by complex factors. Our study reports extensive new diversity in a gene of longstanding ecological interest, offers new sources of variation to be explored in functional assays in future study, and advances our understanding of the processes of molecular evolution. The Royal Society 2023-07-12 /pmc/articles/PMC10336374/ /pubmed/37448478 http://dx.doi.org/10.1098/rsos.230451 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Genetics and Genomics
Pinto, Swellan L.
Janiak, Mareike C.
Dutyschaever, Gwen
Barros, Marília A. S.
Chavarria, Adrian Guadamuz
Martin, Maria Pia
Tuh, Fred Y. Y.
Valverde, Carmen Soto
Sims, Lisa M.
Barclay, Robert M. R.
Wells, Konstans
Dominy, Nathaniel J.
Pessoa, Daniel M. A.
Carrigan, Matthew A.
Melin, Amanda D.
Diet and the evolution of ADH7 across seven orders of mammals
title Diet and the evolution of ADH7 across seven orders of mammals
title_full Diet and the evolution of ADH7 across seven orders of mammals
title_fullStr Diet and the evolution of ADH7 across seven orders of mammals
title_full_unstemmed Diet and the evolution of ADH7 across seven orders of mammals
title_short Diet and the evolution of ADH7 across seven orders of mammals
title_sort diet and the evolution of adh7 across seven orders of mammals
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336374/
https://www.ncbi.nlm.nih.gov/pubmed/37448478
http://dx.doi.org/10.1098/rsos.230451
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