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Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
Nutrient intake and avoidance of toxins are essential for survival and controlled by attractive and aversive feeding responses. Drosophila melanogaster presents one of the best characterized systems for studies on chemosensation, which is mediated by multigene families of chemoreceptors, including o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894858/ https://www.ncbi.nlm.nih.gov/pubmed/24302688 http://dx.doi.org/10.1093/chemse/bjt061 |
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author | Swarup, Shilpa Morozova, Tatiana V. Sridhar, Sruthipriya Nokes, Michael Anholt, Robert R.H. |
author_facet | Swarup, Shilpa Morozova, Tatiana V. Sridhar, Sruthipriya Nokes, Michael Anholt, Robert R.H. |
author_sort | Swarup, Shilpa |
collection | PubMed |
description | Nutrient intake and avoidance of toxins are essential for survival and controlled by attractive and aversive feeding responses. Drosophila melanogaster presents one of the best characterized systems for studies on chemosensation, which is mediated by multigene families of chemoreceptors, including olfactory receptors, gustatory receptors, and odorant-binding proteins (OBPs). Although the response profiles of gustatory receptors have been well studied, the contribution of OBPs to food intake is largely unknown. As most aversive (“bitter”) tastants are hydrophobic, we hypothesized that OBPs may fulfill an essential function in transporting bitter tastants to gustatory receptors to modulate feeding behavior. Here, we used 16 RNAi lines that inhibit expression of individual target Obp genes and show that OBPs modulate sucrose intake in response to a panel of nine bitter compounds. Similar to their function in olfaction, OBPs appear to interact with bitter compounds in a combinatorial and sex-dependent manner. RNAi-mediated reduction in expression of individual Obp genes resulted either in enhanced or reduced intake of sucrose in the presence of bitter compounds, consistent with roles for OBPs in transporting tastants to bitter taste receptors, sequestering them to limit their access to these receptors, or interacting directly with gustatory neurons that respond to sucrose. |
format | Online Article Text |
id | pubmed-3894858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38948582014-01-21 Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster Swarup, Shilpa Morozova, Tatiana V. Sridhar, Sruthipriya Nokes, Michael Anholt, Robert R.H. Chem Senses Original Article Nutrient intake and avoidance of toxins are essential for survival and controlled by attractive and aversive feeding responses. Drosophila melanogaster presents one of the best characterized systems for studies on chemosensation, which is mediated by multigene families of chemoreceptors, including olfactory receptors, gustatory receptors, and odorant-binding proteins (OBPs). Although the response profiles of gustatory receptors have been well studied, the contribution of OBPs to food intake is largely unknown. As most aversive (“bitter”) tastants are hydrophobic, we hypothesized that OBPs may fulfill an essential function in transporting bitter tastants to gustatory receptors to modulate feeding behavior. Here, we used 16 RNAi lines that inhibit expression of individual target Obp genes and show that OBPs modulate sucrose intake in response to a panel of nine bitter compounds. Similar to their function in olfaction, OBPs appear to interact with bitter compounds in a combinatorial and sex-dependent manner. RNAi-mediated reduction in expression of individual Obp genes resulted either in enhanced or reduced intake of sucrose in the presence of bitter compounds, consistent with roles for OBPs in transporting tastants to bitter taste receptors, sequestering them to limit their access to these receptors, or interacting directly with gustatory neurons that respond to sucrose. Oxford University Press 2014-02 2013-12-03 /pmc/articles/PMC3894858/ /pubmed/24302688 http://dx.doi.org/10.1093/chemse/bjt061 Text en © The Author 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), 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 | Original Article Swarup, Shilpa Morozova, Tatiana V. Sridhar, Sruthipriya Nokes, Michael Anholt, Robert R.H. Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster |
title | Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
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title_full | Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
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title_fullStr | Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
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title_full_unstemmed | Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
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title_short | Modulation of Feeding Behavior by Odorant-Binding Proteins in Drosophila melanogaster
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title_sort | modulation of feeding behavior by odorant-binding proteins in drosophila melanogaster |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894858/ https://www.ncbi.nlm.nih.gov/pubmed/24302688 http://dx.doi.org/10.1093/chemse/bjt061 |
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