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A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight
Insect flight is regulated by various sensory inputs and neuromodulatory circuits which function in synchrony to control and fine-tune the final behavioral outcome. The cellular and molecular bases of flight neuromodulatory circuits are not well defined. In Drosophila melanogaster, it is known that...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789835/ https://www.ncbi.nlm.nih.gov/pubmed/24098151 http://dx.doi.org/10.1371/journal.pgen.1003849 |
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author | Agrawal, Tarjani Sadaf, Sufia Hasan, Gaiti |
author_facet | Agrawal, Tarjani Sadaf, Sufia Hasan, Gaiti |
author_sort | Agrawal, Tarjani |
collection | PubMed |
description | Insect flight is regulated by various sensory inputs and neuromodulatory circuits which function in synchrony to control and fine-tune the final behavioral outcome. The cellular and molecular bases of flight neuromodulatory circuits are not well defined. In Drosophila melanogaster, it is known that neuronal IP(3) receptor mediated Ca(2+) signaling and store-operated Ca(2+) entry (SOCE) are required for air-puff stimulated adult flight. However, G-protein coupled receptors (GPCRs) that activate intracellular Ca(2+) signaling in the context of flight are unknown in Drosophila. We performed a genetic RNAi screen to identify GPCRs that regulate flight by activating the IP(3) receptor. Among the 108 GPCRs screened, we discovered 5 IP(3)/Ca(2+) linked GPCRs that are necessary for maintenance of air-puff stimulated flight. Analysis of their temporal requirement established that while some GPCRs are required only during flight circuit development, others are required both in pupal development as well as during adult flight. Interestingly, our study identified the Pigment Dispersing Factor Receptor (PdfR) as a regulator of flight circuit development and as a modulator of acute flight. From the analysis of PdfR expressing neurons relevant for flight and its well-defined roles in other behavioral paradigms, we propose that PdfR signaling functions systemically to integrate multiple sensory inputs and modulate downstream motor behavior. |
format | Online Article Text |
id | pubmed-3789835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37898352013-10-04 A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight Agrawal, Tarjani Sadaf, Sufia Hasan, Gaiti PLoS Genet Research Article Insect flight is regulated by various sensory inputs and neuromodulatory circuits which function in synchrony to control and fine-tune the final behavioral outcome. The cellular and molecular bases of flight neuromodulatory circuits are not well defined. In Drosophila melanogaster, it is known that neuronal IP(3) receptor mediated Ca(2+) signaling and store-operated Ca(2+) entry (SOCE) are required for air-puff stimulated adult flight. However, G-protein coupled receptors (GPCRs) that activate intracellular Ca(2+) signaling in the context of flight are unknown in Drosophila. We performed a genetic RNAi screen to identify GPCRs that regulate flight by activating the IP(3) receptor. Among the 108 GPCRs screened, we discovered 5 IP(3)/Ca(2+) linked GPCRs that are necessary for maintenance of air-puff stimulated flight. Analysis of their temporal requirement established that while some GPCRs are required only during flight circuit development, others are required both in pupal development as well as during adult flight. Interestingly, our study identified the Pigment Dispersing Factor Receptor (PdfR) as a regulator of flight circuit development and as a modulator of acute flight. From the analysis of PdfR expressing neurons relevant for flight and its well-defined roles in other behavioral paradigms, we propose that PdfR signaling functions systemically to integrate multiple sensory inputs and modulate downstream motor behavior. Public Library of Science 2013-10-03 /pmc/articles/PMC3789835/ /pubmed/24098151 http://dx.doi.org/10.1371/journal.pgen.1003849 Text en © 2013 Agrawal 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 Agrawal, Tarjani Sadaf, Sufia Hasan, Gaiti A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title | A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title_full | A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title_fullStr | A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title_full_unstemmed | A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title_short | A Genetic RNAi Screen for IP(3)/Ca(2+) Coupled GPCRs in Drosophila Identifies the PdfR as a Regulator of Insect Flight |
title_sort | genetic rnai screen for ip(3)/ca(2+) coupled gpcrs in drosophila identifies the pdfr as a regulator of insect flight |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789835/ https://www.ncbi.nlm.nih.gov/pubmed/24098151 http://dx.doi.org/10.1371/journal.pgen.1003849 |
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