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Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals

Dietary shifts can drive molecular evolution in mammals and a major transition in human history, the agricultural revolution, favored carbohydrate consumption. We investigated the evolutionary history of nine genes encoding brush-border proteins involved in carbohydrate digestion/absorption. Results...

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Autores principales: Pontremoli, Chiara, Mozzi, Alessandra, Forni, Diego, Cagliani, Rachele, Pozzoli, Uberto, Menozzi, Giorgia, Vertemara, Jacopo, Bresolin, Nereo, Clerici, Mario, Sironi, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607523/
https://www.ncbi.nlm.nih.gov/pubmed/26319403
http://dx.doi.org/10.1093/gbe/evv166
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author Pontremoli, Chiara
Mozzi, Alessandra
Forni, Diego
Cagliani, Rachele
Pozzoli, Uberto
Menozzi, Giorgia
Vertemara, Jacopo
Bresolin, Nereo
Clerici, Mario
Sironi, Manuela
author_facet Pontremoli, Chiara
Mozzi, Alessandra
Forni, Diego
Cagliani, Rachele
Pozzoli, Uberto
Menozzi, Giorgia
Vertemara, Jacopo
Bresolin, Nereo
Clerici, Mario
Sironi, Manuela
author_sort Pontremoli, Chiara
collection PubMed
description Dietary shifts can drive molecular evolution in mammals and a major transition in human history, the agricultural revolution, favored carbohydrate consumption. We investigated the evolutionary history of nine genes encoding brush-border proteins involved in carbohydrate digestion/absorption. Results indicated widespread adaptive evolution in mammals, with several branches experiencing episodic selection, particularly strong in bats. Many positively selected sites map to functional protein regions (e.g., within glucosidase catalytic crevices), with parallel evolution at SI (sucrase-isomaltase) and MGAM (maltase-glucoamylase). In human populations, five genes were targeted by positive selection acting on noncoding variants within regulatory elements. Analysis of ancient DNA samples indicated that most derived alleles were already present in the Paleolithic. Positively selected variants at SLC2A5 (fructose transporter) were an exception and possibly spread following the domestication of specific fruit crops. We conclude that agriculture determined no major selective event at carbohydrate metabolism genes in humans, with implications for susceptibility to metabolic disorders.
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spelling pubmed-46075232015-10-19 Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals Pontremoli, Chiara Mozzi, Alessandra Forni, Diego Cagliani, Rachele Pozzoli, Uberto Menozzi, Giorgia Vertemara, Jacopo Bresolin, Nereo Clerici, Mario Sironi, Manuela Genome Biol Evol Research Article Dietary shifts can drive molecular evolution in mammals and a major transition in human history, the agricultural revolution, favored carbohydrate consumption. We investigated the evolutionary history of nine genes encoding brush-border proteins involved in carbohydrate digestion/absorption. Results indicated widespread adaptive evolution in mammals, with several branches experiencing episodic selection, particularly strong in bats. Many positively selected sites map to functional protein regions (e.g., within glucosidase catalytic crevices), with parallel evolution at SI (sucrase-isomaltase) and MGAM (maltase-glucoamylase). In human populations, five genes were targeted by positive selection acting on noncoding variants within regulatory elements. Analysis of ancient DNA samples indicated that most derived alleles were already present in the Paleolithic. Positively selected variants at SLC2A5 (fructose transporter) were an exception and possibly spread following the domestication of specific fruit crops. We conclude that agriculture determined no major selective event at carbohydrate metabolism genes in humans, with implications for susceptibility to metabolic disorders. Oxford University Press 2015-09-11 /pmc/articles/PMC4607523/ /pubmed/26319403 http://dx.doi.org/10.1093/gbe/evv166 Text en © The Author(s) 2015. 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 Research Article
Pontremoli, Chiara
Mozzi, Alessandra
Forni, Diego
Cagliani, Rachele
Pozzoli, Uberto
Menozzi, Giorgia
Vertemara, Jacopo
Bresolin, Nereo
Clerici, Mario
Sironi, Manuela
Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title_full Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title_fullStr Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title_full_unstemmed Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title_short Natural Selection at the Brush-Border: Adaptations to Carbohydrate Diets in Humans and Other Mammals
title_sort natural selection at the brush-border: adaptations to carbohydrate diets in humans and other mammals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607523/
https://www.ncbi.nlm.nih.gov/pubmed/26319403
http://dx.doi.org/10.1093/gbe/evv166
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