Cargando…
A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila
Sleep is an essential behavioral state of rest that is regulated by homeostatic drives to ensure a balance of sleep and activity, as well as independent arousal mechanisms in the central brain. Dopamine has been identified as a critical regulator of both sleep behavior and arousal. Here, we present...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144989/ https://www.ncbi.nlm.nih.gov/pubmed/27760793 http://dx.doi.org/10.1534/g3.116.032136 |
_version_ | 1782473219434872832 |
---|---|
author | Jiang, Yiqin Pitmon, Elise Berry, Jack Wolf, Fred W. McKenzie, Zach Lebestky, Tim J. |
author_facet | Jiang, Yiqin Pitmon, Elise Berry, Jack Wolf, Fred W. McKenzie, Zach Lebestky, Tim J. |
author_sort | Jiang, Yiqin |
collection | PubMed |
description | Sleep is an essential behavioral state of rest that is regulated by homeostatic drives to ensure a balance of sleep and activity, as well as independent arousal mechanisms in the central brain. Dopamine has been identified as a critical regulator of both sleep behavior and arousal. Here, we present results of a genetic screen that selectively restored the Dopamine Receptor (DopR/DopR1/dumb) to specific neuroanatomical regions of the adult Drosophila brain to assess requirements for DopR in sleep behavior. We have identified subsets of the mushroom body that utilizes DopR in daytime sleep regulation. These data are supported by multiple examples of spatially restricted genetic rescue data in discrete circuits of the mushroom body, as well as immunohistochemistry that corroborates the localization of DopR protein within mushroom body circuits. Independent loss of function data using an inducible RNAi construct in the same specific circuits also supports a requirement for DopR in daytime sleep. Additional circuit activation of discrete DopR(+) mushroom body neurons also suggests roles for these subpopulations in sleep behavior. These conclusions support a new separable function for DopR in daytime sleep regulation within the mushroom body. This daytime regulation is independent of the known role of DopR in nighttime sleep, which is regulated within the Fan-Shaped Body (FSB). This study provides new neuroanatomical loci for exploration of dopaminergic sleep functions in Drosophila, and expands our understanding of sleep regulation during the day vs. night. |
format | Online Article Text |
id | pubmed-5144989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-51449892016-12-09 A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila Jiang, Yiqin Pitmon, Elise Berry, Jack Wolf, Fred W. McKenzie, Zach Lebestky, Tim J. G3 (Bethesda) Mutant Screen Reports Sleep is an essential behavioral state of rest that is regulated by homeostatic drives to ensure a balance of sleep and activity, as well as independent arousal mechanisms in the central brain. Dopamine has been identified as a critical regulator of both sleep behavior and arousal. Here, we present results of a genetic screen that selectively restored the Dopamine Receptor (DopR/DopR1/dumb) to specific neuroanatomical regions of the adult Drosophila brain to assess requirements for DopR in sleep behavior. We have identified subsets of the mushroom body that utilizes DopR in daytime sleep regulation. These data are supported by multiple examples of spatially restricted genetic rescue data in discrete circuits of the mushroom body, as well as immunohistochemistry that corroborates the localization of DopR protein within mushroom body circuits. Independent loss of function data using an inducible RNAi construct in the same specific circuits also supports a requirement for DopR in daytime sleep. Additional circuit activation of discrete DopR(+) mushroom body neurons also suggests roles for these subpopulations in sleep behavior. These conclusions support a new separable function for DopR in daytime sleep regulation within the mushroom body. This daytime regulation is independent of the known role of DopR in nighttime sleep, which is regulated within the Fan-Shaped Body (FSB). This study provides new neuroanatomical loci for exploration of dopaminergic sleep functions in Drosophila, and expands our understanding of sleep regulation during the day vs. night. Genetics Society of America 2016-10-18 /pmc/articles/PMC5144989/ /pubmed/27760793 http://dx.doi.org/10.1534/g3.116.032136 Text en Copyright © 2016 Jiang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Mutant Screen Reports Jiang, Yiqin Pitmon, Elise Berry, Jack Wolf, Fred W. McKenzie, Zach Lebestky, Tim J. A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title | A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title_full | A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title_fullStr | A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title_full_unstemmed | A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title_short | A Genetic Screen To Assess Dopamine Receptor (DopR1) Dependent Sleep Regulation in Drosophila |
title_sort | genetic screen to assess dopamine receptor (dopr1) dependent sleep regulation in drosophila |
topic | Mutant Screen Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144989/ https://www.ncbi.nlm.nih.gov/pubmed/27760793 http://dx.doi.org/10.1534/g3.116.032136 |
work_keys_str_mv | AT jiangyiqin ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT pitmonelise ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT berryjack ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT wolffredw ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT mckenziezach ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT lebestkytimj ageneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT jiangyiqin geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT pitmonelise geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT berryjack geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT wolffredw geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT mckenziezach geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila AT lebestkytimj geneticscreentoassessdopaminereceptordopr1dependentsleepregulationindrosophila |