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Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Br...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508045/ https://www.ncbi.nlm.nih.gov/pubmed/26193363 http://dx.doi.org/10.1371/journal.pone.0133083 |
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author | Kohyama-Koganeya, Ayako Kurosawa, Mizuki Hirabayashi, Yoshio |
author_facet | Kohyama-Koganeya, Ayako Kurosawa, Mizuki Hirabayashi, Yoshio |
author_sort | Kohyama-Koganeya, Ayako |
collection | PubMed |
description | Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Bride of sevenless (BOSS) is a highly evolutionarily conserved protein that responds to extracellular glucose levels in order to regulate energy homeostasis. To address how BOSS regulates energy homeostasis, we characterized a boss mutant by assessing its food intake and stored energy levels. Boss mutants exhibited increased food intake but decreased stored triacylglyceride levels. Using boss-GAL4 drivers, we found that boss is expressed in select tissues that are involved in nutrient sensing and food intake, in a subset of neurons in brain and chemosensory organs, in fat body, and in endocrine cells in gut (enteroendocrine cells). Flies with tissue-specific boss knockdowns in these tissues had abnormal stored energy levels and abnormal food intake. These results suggest that BOSS in either neurons or peripheral nutrient-sensing tissues affects energy homeostasis in ways that relate to the sensing of nutrients and regulation of food intake. |
format | Online Article Text |
id | pubmed-4508045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45080452015-07-24 Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism Kohyama-Koganeya, Ayako Kurosawa, Mizuki Hirabayashi, Yoshio PLoS One Research Article Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Bride of sevenless (BOSS) is a highly evolutionarily conserved protein that responds to extracellular glucose levels in order to regulate energy homeostasis. To address how BOSS regulates energy homeostasis, we characterized a boss mutant by assessing its food intake and stored energy levels. Boss mutants exhibited increased food intake but decreased stored triacylglyceride levels. Using boss-GAL4 drivers, we found that boss is expressed in select tissues that are involved in nutrient sensing and food intake, in a subset of neurons in brain and chemosensory organs, in fat body, and in endocrine cells in gut (enteroendocrine cells). Flies with tissue-specific boss knockdowns in these tissues had abnormal stored energy levels and abnormal food intake. These results suggest that BOSS in either neurons or peripheral nutrient-sensing tissues affects energy homeostasis in ways that relate to the sensing of nutrients and regulation of food intake. Public Library of Science 2015-07-20 /pmc/articles/PMC4508045/ /pubmed/26193363 http://dx.doi.org/10.1371/journal.pone.0133083 Text en © 2015 Kohyama-Koganeya 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 Kohyama-Koganeya, Ayako Kurosawa, Mizuki Hirabayashi, Yoshio Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title | Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title_full | Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title_fullStr | Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title_full_unstemmed | Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title_short | Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism |
title_sort | differential effects of tissue-specific deletion of boss on feeding behaviors and energy metabolism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508045/ https://www.ncbi.nlm.nih.gov/pubmed/26193363 http://dx.doi.org/10.1371/journal.pone.0133083 |
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