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Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster

The detection and processing of chemical stimuli involve coordinated neuronal networks that process sensory information. This allows animals, such as the model species Drosophila melanogaster, to detect food sources and to choose a potential mate. In peripheral olfactory tissues, several classes of...

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Autores principales: Fraichard, Stéphane, Legendre, Arièle, Lucas, Philippe, Chauvel, Isabelle, Faure, Philippe, Neiers, Fabrice, Artur, Yves, Briand, Loïc, Ferveur, Jean-François, Heydel, Jean-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140800/
https://www.ncbi.nlm.nih.gov/pubmed/32106439
http://dx.doi.org/10.3390/genes11030237
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author Fraichard, Stéphane
Legendre, Arièle
Lucas, Philippe
Chauvel, Isabelle
Faure, Philippe
Neiers, Fabrice
Artur, Yves
Briand, Loïc
Ferveur, Jean-François
Heydel, Jean-Marie
author_facet Fraichard, Stéphane
Legendre, Arièle
Lucas, Philippe
Chauvel, Isabelle
Faure, Philippe
Neiers, Fabrice
Artur, Yves
Briand, Loïc
Ferveur, Jean-François
Heydel, Jean-Marie
author_sort Fraichard, Stéphane
collection PubMed
description The detection and processing of chemical stimuli involve coordinated neuronal networks that process sensory information. This allows animals, such as the model species Drosophila melanogaster, to detect food sources and to choose a potential mate. In peripheral olfactory tissues, several classes of proteins are acting to modulate the detection of chemosensory signals. This includes odorant-binding proteins together with odorant-degrading enzymes (ODEs). These enzymes, which primarily act to eliminate toxic compounds from the whole organism also modulate chemodetection. ODEs are thought to neutralize the stimulus molecule concurrently to its detection, avoiding receptor saturation thus allowing chemosensory neurons to respond to the next stimulus. Here, we show that one UDP-glycosyltransferase (UGT36E1) expressed in D. melanogaster antennal olfactory sensory neurons (OSNs) is involved in sex pheromone discrimination. UGT36E1 overexpression caused by an insertion mutation affected male behavioral ability to discriminate sex pheromones while it increased OSN electrophysiological activity to male pheromones. Reciprocally, the decreased expression of UGT36E1, controlled by an RNAi transgene, improved male ability to discriminate sex pheromones whereas it decreased electrophysiological activity in the relevant OSNs. When we combined the two genotypes (mutation and RNAi), we restored wild-type-like levels both for the behavioral discrimination and UGT36E1 expression. Taken together, our results strongly suggest that this UGT plays a pivotal role in Drosophila pheromonal detection.
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spelling pubmed-71408002020-04-10 Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster Fraichard, Stéphane Legendre, Arièle Lucas, Philippe Chauvel, Isabelle Faure, Philippe Neiers, Fabrice Artur, Yves Briand, Loïc Ferveur, Jean-François Heydel, Jean-Marie Genes (Basel) Article The detection and processing of chemical stimuli involve coordinated neuronal networks that process sensory information. This allows animals, such as the model species Drosophila melanogaster, to detect food sources and to choose a potential mate. In peripheral olfactory tissues, several classes of proteins are acting to modulate the detection of chemosensory signals. This includes odorant-binding proteins together with odorant-degrading enzymes (ODEs). These enzymes, which primarily act to eliminate toxic compounds from the whole organism also modulate chemodetection. ODEs are thought to neutralize the stimulus molecule concurrently to its detection, avoiding receptor saturation thus allowing chemosensory neurons to respond to the next stimulus. Here, we show that one UDP-glycosyltransferase (UGT36E1) expressed in D. melanogaster antennal olfactory sensory neurons (OSNs) is involved in sex pheromone discrimination. UGT36E1 overexpression caused by an insertion mutation affected male behavioral ability to discriminate sex pheromones while it increased OSN electrophysiological activity to male pheromones. Reciprocally, the decreased expression of UGT36E1, controlled by an RNAi transgene, improved male ability to discriminate sex pheromones whereas it decreased electrophysiological activity in the relevant OSNs. When we combined the two genotypes (mutation and RNAi), we restored wild-type-like levels both for the behavioral discrimination and UGT36E1 expression. Taken together, our results strongly suggest that this UGT plays a pivotal role in Drosophila pheromonal detection. MDPI 2020-02-25 /pmc/articles/PMC7140800/ /pubmed/32106439 http://dx.doi.org/10.3390/genes11030237 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fraichard, Stéphane
Legendre, Arièle
Lucas, Philippe
Chauvel, Isabelle
Faure, Philippe
Neiers, Fabrice
Artur, Yves
Briand, Loïc
Ferveur, Jean-François
Heydel, Jean-Marie
Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title_full Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title_fullStr Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title_full_unstemmed Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title_short Modulation of Sex Pheromone Discrimination by a UDP-Glycosyltransferase in Drosophila melanogaster
title_sort modulation of sex pheromone discrimination by a udp-glycosyltransferase in drosophila melanogaster
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140800/
https://www.ncbi.nlm.nih.gov/pubmed/32106439
http://dx.doi.org/10.3390/genes11030237
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