Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats

Abstract By generating raw genetic material and diverse biological functions, gene duplication represents a major evolutionary mechanism that is of fundamental importance in ecological adaptation. The lineage‐specific duplication events of bitter taste receptor genes ( Tas2r s) have been identified...

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Published in:Molecular Ecology
Main Authors: Jiao, Hengwu, Wang, Yi, Zhang, Libiao, Jiang, Peihua, Zhao, Huabin
Other Authors: National Natural Science Foundation of China, National Institutes of Health
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2018
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Online Access:http://dx.doi.org/10.1111/mec.14873
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spelling crwiley:10.1111/mec.14873 2024-06-23T07:47:47+00:00 Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats Jiao, Hengwu Wang, Yi Zhang, Libiao Jiang, Peihua Zhao, Huabin National Natural Science Foundation of China National Institutes of Health 2018 http://dx.doi.org/10.1111/mec.14873 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fmec.14873 https://onlinelibrary.wiley.com/doi/pdf/10.1111/mec.14873 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Molecular Ecology volume 27, issue 22, page 4475-4488 ISSN 0962-1083 1365-294X journal-article 2018 crwiley https://doi.org/10.1111/mec.14873 2024-06-06T04:22:38Z Abstract By generating raw genetic material and diverse biological functions, gene duplication represents a major evolutionary mechanism that is of fundamental importance in ecological adaptation. The lineage‐specific duplication events of bitter taste receptor genes ( Tas2r s) have been identified in a number of vertebrates, but functional evolution of new Tas2r copies after duplication remains largely unknown. Here, we present the largest data set of bat Tas2r s to date, identified from existing genome sequences of 15 bat species and newly sequenced from 17 bat species, and demonstrate lineage‐specific duplications of Tas2r16 , Tas2r18 and Tas2r41 that only occurred in Myotis bats. Myotis bats are highly speciose and represent the only mammalian genus that is naturally distributed on every continent except Antarctica. The occupation of such diverse habitats might have driven the Tas2r gene expansion. New copies of Tas2r s in Myotis bats have shown molecular adaptation and functional divergence. For example, three copies of Tas2r16 in Myotis davidii showed differential sensitivities to arbutin and salicin that may occur in their insect prey, as suggested by cell‐based functional assays. We hypothesize that functional differences among Tas2r copies in Myotis bats would increase their survival rate through preventing the ingestion of an elevated number of bitter‐tasting dietary toxins from their insect prey, which may have facilitated their adaptation to diverse habitats. Our study demonstrates functional changes of new Tas2r copies after lineage‐specific duplications in Myotis bats and highlights the potential role of taste perception in exploiting new environments. Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Molecular Ecology 27 22 4475 4488
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract By generating raw genetic material and diverse biological functions, gene duplication represents a major evolutionary mechanism that is of fundamental importance in ecological adaptation. The lineage‐specific duplication events of bitter taste receptor genes ( Tas2r s) have been identified in a number of vertebrates, but functional evolution of new Tas2r copies after duplication remains largely unknown. Here, we present the largest data set of bat Tas2r s to date, identified from existing genome sequences of 15 bat species and newly sequenced from 17 bat species, and demonstrate lineage‐specific duplications of Tas2r16 , Tas2r18 and Tas2r41 that only occurred in Myotis bats. Myotis bats are highly speciose and represent the only mammalian genus that is naturally distributed on every continent except Antarctica. The occupation of such diverse habitats might have driven the Tas2r gene expansion. New copies of Tas2r s in Myotis bats have shown molecular adaptation and functional divergence. For example, three copies of Tas2r16 in Myotis davidii showed differential sensitivities to arbutin and salicin that may occur in their insect prey, as suggested by cell‐based functional assays. We hypothesize that functional differences among Tas2r copies in Myotis bats would increase their survival rate through preventing the ingestion of an elevated number of bitter‐tasting dietary toxins from their insect prey, which may have facilitated their adaptation to diverse habitats. Our study demonstrates functional changes of new Tas2r copies after lineage‐specific duplications in Myotis bats and highlights the potential role of taste perception in exploiting new environments.
author2 National Natural Science Foundation of China
National Institutes of Health
format Article in Journal/Newspaper
author Jiao, Hengwu
Wang, Yi
Zhang, Libiao
Jiang, Peihua
Zhao, Huabin
spellingShingle Jiao, Hengwu
Wang, Yi
Zhang, Libiao
Jiang, Peihua
Zhao, Huabin
Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
author_facet Jiao, Hengwu
Wang, Yi
Zhang, Libiao
Jiang, Peihua
Zhao, Huabin
author_sort Jiao, Hengwu
title Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
title_short Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
title_full Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
title_fullStr Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
title_full_unstemmed Lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
title_sort lineage‐specific duplication and adaptive evolution of bitter taste receptor genes in bats
publisher Wiley
publishDate 2018
url http://dx.doi.org/10.1111/mec.14873
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fmec.14873
https://onlinelibrary.wiley.com/doi/pdf/10.1111/mec.14873
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Molecular Ecology
volume 27, issue 22, page 4475-4488
ISSN 0962-1083 1365-294X
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1111/mec.14873
container_title Molecular Ecology
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container_issue 22
container_start_page 4475
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