Cargando…

Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations

BACKGROUND: Using fungiform (FG) and circumvallate (CV) taste buds isolated by laser capture microdissection and analyzed using gene arrays, we previously constructed a comprehensive database of gene expression in primates, which revealed over 2,300 taste bud-associated genes. Bioinformatics analyse...

Descripción completa

Detalles Bibliográficos
Autores principales: Moyer, Bryan D., Hevezi, Peter, Gao, Na, Lu, Min, Kalabat, Dalia, Soto, Hortensia, Echeverri, Fernando, Laita, Bianca, Yeh, Shaoyang Anthony, Zoller, Mark, Zlotnik, Albert
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780358/
https://www.ncbi.nlm.nih.gov/pubmed/19997627
http://dx.doi.org/10.1371/journal.pone.0007682
_version_ 1782174472669757440
author Moyer, Bryan D.
Hevezi, Peter
Gao, Na
Lu, Min
Kalabat, Dalia
Soto, Hortensia
Echeverri, Fernando
Laita, Bianca
Yeh, Shaoyang Anthony
Zoller, Mark
Zlotnik, Albert
author_facet Moyer, Bryan D.
Hevezi, Peter
Gao, Na
Lu, Min
Kalabat, Dalia
Soto, Hortensia
Echeverri, Fernando
Laita, Bianca
Yeh, Shaoyang Anthony
Zoller, Mark
Zlotnik, Albert
author_sort Moyer, Bryan D.
collection PubMed
description BACKGROUND: Using fungiform (FG) and circumvallate (CV) taste buds isolated by laser capture microdissection and analyzed using gene arrays, we previously constructed a comprehensive database of gene expression in primates, which revealed over 2,300 taste bud-associated genes. Bioinformatics analyses identified hundreds of genes predicted to encode multi-transmembrane domain proteins with no previous association with taste function. A first step in elucidating the roles these gene products play in gustation is to identify the specific taste cell types in which they are expressed. METHODOLOGY/PRINCIPAL FINDINGS: Using double label in situ hybridization analyses, we identified seven new genes expressed in specific taste cell types, including sweet, bitter, and umami cells (TRPM5-positive), sour cells (PKD2L1-positive), as well as other taste cell populations. Transmembrane protein 44 (TMEM44), a protein with seven predicted transmembrane domains with no homology to GPCRs, is expressed in a TRPM5-negative and PKD2L1-negative population that is enriched in the bottom portion of taste buds and may represent developmentally immature taste cells. Calcium homeostasis modulator 1 (CALHM1), a component of a novel calcium channel, along with family members CALHM2 and CALHM3; multiple C2 domains; transmembrane 1 (MCTP1), a calcium-binding transmembrane protein; and anoctamin 7 (ANO7), a member of the recently identified calcium-gated chloride channel family, are all expressed in TRPM5 cells. These proteins may modulate and effect calcium signalling stemming from sweet, bitter, and umami receptor activation. Synaptic vesicle glycoprotein 2B (SV2B), a regulator of synaptic vesicle exocytosis, is expressed in PKD2L1 cells, suggesting that this taste cell population transmits tastant information to gustatory afferent nerve fibers via exocytic neurotransmitter release. CONCLUSIONS/SIGNIFICANCE: Identification of genes encoding multi-transmembrane domain proteins expressed in primate taste buds provides new insights into the processes of taste cell development, signal transduction, and information coding. Discrete taste cell populations exhibit highly specific gene expression patterns, supporting a model whereby each mature taste receptor cell is responsible for sensing, transmitting, and coding a specific taste quality.
format Text
id pubmed-2780358
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-27803582009-12-08 Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations Moyer, Bryan D. Hevezi, Peter Gao, Na Lu, Min Kalabat, Dalia Soto, Hortensia Echeverri, Fernando Laita, Bianca Yeh, Shaoyang Anthony Zoller, Mark Zlotnik, Albert PLoS One Research Article BACKGROUND: Using fungiform (FG) and circumvallate (CV) taste buds isolated by laser capture microdissection and analyzed using gene arrays, we previously constructed a comprehensive database of gene expression in primates, which revealed over 2,300 taste bud-associated genes. Bioinformatics analyses identified hundreds of genes predicted to encode multi-transmembrane domain proteins with no previous association with taste function. A first step in elucidating the roles these gene products play in gustation is to identify the specific taste cell types in which they are expressed. METHODOLOGY/PRINCIPAL FINDINGS: Using double label in situ hybridization analyses, we identified seven new genes expressed in specific taste cell types, including sweet, bitter, and umami cells (TRPM5-positive), sour cells (PKD2L1-positive), as well as other taste cell populations. Transmembrane protein 44 (TMEM44), a protein with seven predicted transmembrane domains with no homology to GPCRs, is expressed in a TRPM5-negative and PKD2L1-negative population that is enriched in the bottom portion of taste buds and may represent developmentally immature taste cells. Calcium homeostasis modulator 1 (CALHM1), a component of a novel calcium channel, along with family members CALHM2 and CALHM3; multiple C2 domains; transmembrane 1 (MCTP1), a calcium-binding transmembrane protein; and anoctamin 7 (ANO7), a member of the recently identified calcium-gated chloride channel family, are all expressed in TRPM5 cells. These proteins may modulate and effect calcium signalling stemming from sweet, bitter, and umami receptor activation. Synaptic vesicle glycoprotein 2B (SV2B), a regulator of synaptic vesicle exocytosis, is expressed in PKD2L1 cells, suggesting that this taste cell population transmits tastant information to gustatory afferent nerve fibers via exocytic neurotransmitter release. CONCLUSIONS/SIGNIFICANCE: Identification of genes encoding multi-transmembrane domain proteins expressed in primate taste buds provides new insights into the processes of taste cell development, signal transduction, and information coding. Discrete taste cell populations exhibit highly specific gene expression patterns, supporting a model whereby each mature taste receptor cell is responsible for sensing, transmitting, and coding a specific taste quality. Public Library of Science 2009-12-04 /pmc/articles/PMC2780358/ /pubmed/19997627 http://dx.doi.org/10.1371/journal.pone.0007682 Text en Moyer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Moyer, Bryan D.
Hevezi, Peter
Gao, Na
Lu, Min
Kalabat, Dalia
Soto, Hortensia
Echeverri, Fernando
Laita, Bianca
Yeh, Shaoyang Anthony
Zoller, Mark
Zlotnik, Albert
Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title_full Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title_fullStr Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title_full_unstemmed Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title_short Expression of Genes Encoding Multi-Transmembrane Proteins in Specific Primate Taste Cell Populations
title_sort expression of genes encoding multi-transmembrane proteins in specific primate taste cell populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780358/
https://www.ncbi.nlm.nih.gov/pubmed/19997627
http://dx.doi.org/10.1371/journal.pone.0007682
work_keys_str_mv AT moyerbryand expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT hevezipeter expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT gaona expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT lumin expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT kalabatdalia expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT sotohortensia expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT echeverrifernando expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT laitabianca expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT yehshaoyanganthony expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT zollermark expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations
AT zlotnikalbert expressionofgenesencodingmultitransmembraneproteinsinspecificprimatetastecellpopulations