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Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals

Diet is a key factor in determining and structuring animal diversity and adaptive radiations. The mammalian fossil record preserves phenotypic evidence of many dietary shifts, whereas genetic changes followed by dietary diversification in mammals remain largely unknown. To test whether living mammal...

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Autores principales: Jiao, Hengwu, Zhang, Libiao, Xie, Huan-Wang, Simmons, Nancy B, Liu, Hui, Zhao, Huabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759077/
https://www.ncbi.nlm.nih.gov/pubmed/31311032
http://dx.doi.org/10.1093/molbev/msz127
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author Jiao, Hengwu
Zhang, Libiao
Xie, Huan-Wang
Simmons, Nancy B
Liu, Hui
Zhao, Huabin
author_facet Jiao, Hengwu
Zhang, Libiao
Xie, Huan-Wang
Simmons, Nancy B
Liu, Hui
Zhao, Huabin
author_sort Jiao, Hengwu
collection PubMed
description Diet is a key factor in determining and structuring animal diversity and adaptive radiations. The mammalian fossil record preserves phenotypic evidence of many dietary shifts, whereas genetic changes followed by dietary diversification in mammals remain largely unknown. To test whether living mammals preserve molecular evidence of dietary shifts, we examined the trehalase gene (Treh), which encodes an enzyme capable of digesting trehalose from insect blood, in bats and other mammals with diverse diets. Bats represent the largest dietary radiation among all mammalian orders, with independent origins of frugivory, nectarivory, carnivory, omnivory, and even sanguivory in an otherwise insectivorous clade. We found that Treh has been inactivated in unrelated bat lineages that independently radiated into noninsectivorous niches. Consistently, purifying selection has been markedly relaxed in noninsectivorous bats compared with their insectivorous relatives. Enzymatic assays of intestinal trehalase in bats suggest that trehalase activity tends to be lost or markedly reduced in noninsectivorous bats compared with their insectivorous relatives. Furthermore, our survey of Treh in 119 mammal species, which represent a deeper evolutionary timeframe, additionally identified a number of other independent losses of Treh in noninsectivorous species, recapitulating the evolutionary pattern that we found in bats. These results document a molecular record of dietary diversification in mammals, and suggest that such molecular signatures of dietary shifts would help us understand both historical and modern changes of animal diets.
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spelling pubmed-67590772019-10-02 Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals Jiao, Hengwu Zhang, Libiao Xie, Huan-Wang Simmons, Nancy B Liu, Hui Zhao, Huabin Mol Biol Evol Discoveries Diet is a key factor in determining and structuring animal diversity and adaptive radiations. The mammalian fossil record preserves phenotypic evidence of many dietary shifts, whereas genetic changes followed by dietary diversification in mammals remain largely unknown. To test whether living mammals preserve molecular evidence of dietary shifts, we examined the trehalase gene (Treh), which encodes an enzyme capable of digesting trehalose from insect blood, in bats and other mammals with diverse diets. Bats represent the largest dietary radiation among all mammalian orders, with independent origins of frugivory, nectarivory, carnivory, omnivory, and even sanguivory in an otherwise insectivorous clade. We found that Treh has been inactivated in unrelated bat lineages that independently radiated into noninsectivorous niches. Consistently, purifying selection has been markedly relaxed in noninsectivorous bats compared with their insectivorous relatives. Enzymatic assays of intestinal trehalase in bats suggest that trehalase activity tends to be lost or markedly reduced in noninsectivorous bats compared with their insectivorous relatives. Furthermore, our survey of Treh in 119 mammal species, which represent a deeper evolutionary timeframe, additionally identified a number of other independent losses of Treh in noninsectivorous species, recapitulating the evolutionary pattern that we found in bats. These results document a molecular record of dietary diversification in mammals, and suggest that such molecular signatures of dietary shifts would help us understand both historical and modern changes of animal diets. Oxford University Press 2019-10 2019-07-16 /pmc/articles/PMC6759077/ /pubmed/31311032 http://dx.doi.org/10.1093/molbev/msz127 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-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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
Jiao, Hengwu
Zhang, Libiao
Xie, Huan-Wang
Simmons, Nancy B
Liu, Hui
Zhao, Huabin
Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title_full Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title_fullStr Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title_full_unstemmed Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title_short Trehalase Gene as a Molecular Signature of Dietary Diversification in Mammals
title_sort trehalase gene as a molecular signature of dietary diversification in mammals
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759077/
https://www.ncbi.nlm.nih.gov/pubmed/31311032
http://dx.doi.org/10.1093/molbev/msz127
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