Literature DB >> 27226572

Comprehensive Analysis of Mouse Bitter Taste Receptors Reveals Different Molecular Receptive Ranges for Orthologous Receptors in Mice and Humans.

Kristina Lossow1, Sandra Hübner1, Natacha Roudnitzky1, Jay P Slack2, Federica Pollastro3, Maik Behrens4, Wolfgang Meyerhof1.   

Abstract

One key to animal survival is the detection and avoidance of potentially harmful compounds by their bitter taste. Variable numbers of taste 2 receptor genes expressed in the gustatory end organs enable bony vertebrates (Euteleostomi) to recognize numerous bitter chemicals. It is believed that the receptive ranges of bitter taste receptor repertoires match the profiles of bitter chemicals that the species encounter in their diets. Human and mouse genomes contain pairs of orthologous bitter receptor genes that have been conserved throughout evolution. Moreover, expansions in both lineages generated species-specific sets of bitter taste receptor genes. It is assumed that the orthologous bitter taste receptor genes mediate the recognition of bitter toxins relevant for both species, whereas the lineage-specific receptors enable the detection of substances differently encountered by mice and humans. By challenging 34 mouse bitter taste receptors with 128 prototypical bitter substances in a heterologous expression system, we identified cognate compounds for 21 receptors, 19 of which were previously orphan receptors. We have demonstrated that mouse taste 2 receptors, like their human counterparts, vary greatly in their breadth of tuning, ranging from very broadly to extremely narrowly tuned receptors. However, when compared with humans, mice possess fewer broadly tuned receptors and an elevated number of narrowly tuned receptors, supporting the idea that a large receptor repertoire is the basis for the evolution of specialized receptors. Moreover, we have demonstrated that sequence-orthologous bitter taste receptors have distinct agonist profiles. Species-specific gene expansions have enabled further diversification of bitter substance recognition spectra.
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  G protein-coupled receptor (GPCR); bitter taste receptor; calcium imaging; cell signaling; heterologous expression; human; mouse

Mesh:

Substances:

Year:  2016        PMID: 27226572      PMCID: PMC4946946          DOI: 10.1074/jbc.M116.718544

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  113 in total

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Authors:  Cedrick D Dotson; Lan Zhang; Hong Xu; Yu-Kyong Shin; Stephan Vigues; Sandra H Ott; Amanda E T Elson; Hyun Jin Choi; Hillary Shaw; Josephine M Egan; Braxton D Mitchell; Xiaodong Li; Nanette I Steinle; Steven D Munger
Journal:  PLoS One       Date:  2008-12-18       Impact factor: 3.240

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Review 4.  Structure-Function Relationships of Olfactory and Taste Receptors.

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Journal:  Chem Senses       Date:  2018-02-02       Impact factor: 3.160

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Journal:  Mol Biol Evol       Date:  2017-07-01       Impact factor: 16.240

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Journal:  J Biol Chem       Date:  2017-04-03       Impact factor: 5.157

9.  Rats are unable to discriminate quinine from diverse bitter stimuli.

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10.  Bitter Taste Responses of Gustducin-positive Taste Cells in Mouse Fungiform and Circumvallate Papillae.

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