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Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors
The Serotonin Transporter (SERT) regulates extracellular serotonin levels and is the target of most current drugs used to treat depression. The mechanisms by which inhibition of SERT activity influences behavior are poorly understood. To address this question in the model organism Drosophila melanog...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721485/ https://www.ncbi.nlm.nih.gov/pubmed/36409783 http://dx.doi.org/10.1371/journal.pgen.1010289 |
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author | Knapp, Elizabeth M. Kaiser, Andrea Arnold, Rebecca C. Sampson, Maureen M. Ruppert, Manuela Xu, Li Anderson, Matthew I. Bonanno, Shivan L. Scholz, Henrike Donlea, Jeffrey M. Krantz, David E. |
author_facet | Knapp, Elizabeth M. Kaiser, Andrea Arnold, Rebecca C. Sampson, Maureen M. Ruppert, Manuela Xu, Li Anderson, Matthew I. Bonanno, Shivan L. Scholz, Henrike Donlea, Jeffrey M. Krantz, David E. |
author_sort | Knapp, Elizabeth M. |
collection | PubMed |
description | The Serotonin Transporter (SERT) regulates extracellular serotonin levels and is the target of most current drugs used to treat depression. The mechanisms by which inhibition of SERT activity influences behavior are poorly understood. To address this question in the model organism Drosophila melanogaster, we developed new loss of function mutations in Drosophila SERT (dSERT). Previous studies in both flies and mammals have implicated serotonin as an important neuromodulator of sleep, and our newly generated dSERT mutants show an increase in total sleep and altered sleep architecture that is mimicked by feeding the SSRI citalopram. Differences in daytime versus nighttime sleep architecture as well as genetic rescue experiments unexpectedly suggest that distinct serotonergic circuits may modulate daytime versus nighttime sleep. dSERT mutants also show defects in copulation and food intake, akin to the clinical side effects of SSRIs and consistent with the pleomorphic influence of serotonin on the behavior of D. melanogaster. Starvation did not overcome the sleep drive in the mutants and in male dSERT mutants, the drive to mate also failed to overcome sleep drive. dSERT may be used to further explore the mechanisms by which serotonin regulates sleep and its interplay with other complex behaviors. |
format | Online Article Text |
id | pubmed-9721485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97214852022-12-06 Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors Knapp, Elizabeth M. Kaiser, Andrea Arnold, Rebecca C. Sampson, Maureen M. Ruppert, Manuela Xu, Li Anderson, Matthew I. Bonanno, Shivan L. Scholz, Henrike Donlea, Jeffrey M. Krantz, David E. PLoS Genet Research Article The Serotonin Transporter (SERT) regulates extracellular serotonin levels and is the target of most current drugs used to treat depression. The mechanisms by which inhibition of SERT activity influences behavior are poorly understood. To address this question in the model organism Drosophila melanogaster, we developed new loss of function mutations in Drosophila SERT (dSERT). Previous studies in both flies and mammals have implicated serotonin as an important neuromodulator of sleep, and our newly generated dSERT mutants show an increase in total sleep and altered sleep architecture that is mimicked by feeding the SSRI citalopram. Differences in daytime versus nighttime sleep architecture as well as genetic rescue experiments unexpectedly suggest that distinct serotonergic circuits may modulate daytime versus nighttime sleep. dSERT mutants also show defects in copulation and food intake, akin to the clinical side effects of SSRIs and consistent with the pleomorphic influence of serotonin on the behavior of D. melanogaster. Starvation did not overcome the sleep drive in the mutants and in male dSERT mutants, the drive to mate also failed to overcome sleep drive. dSERT may be used to further explore the mechanisms by which serotonin regulates sleep and its interplay with other complex behaviors. Public Library of Science 2022-11-21 /pmc/articles/PMC9721485/ /pubmed/36409783 http://dx.doi.org/10.1371/journal.pgen.1010289 Text en © 2022 Knapp et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Knapp, Elizabeth M. Kaiser, Andrea Arnold, Rebecca C. Sampson, Maureen M. Ruppert, Manuela Xu, Li Anderson, Matthew I. Bonanno, Shivan L. Scholz, Henrike Donlea, Jeffrey M. Krantz, David E. Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title | Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title_full | Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title_fullStr | Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title_full_unstemmed | Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title_short | Mutation of the Drosophila melanogaster serotonin transporter dSERT impacts sleep, courtship, and feeding behaviors |
title_sort | mutation of the drosophila melanogaster serotonin transporter dsert impacts sleep, courtship, and feeding behaviors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721485/ https://www.ncbi.nlm.nih.gov/pubmed/36409783 http://dx.doi.org/10.1371/journal.pgen.1010289 |
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