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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

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      PLoS Genetics
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          Abstract

          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.

          Author Summary

          A majority of behavioral patterns in flying insects depend upon their ability to modulate flight. In Drosophila melanogaster, mutations in the IP 3 receptor gene lead to loss of voluntary flight in response to a natural stimulus like a gentle air-puff. From previous genetic and cellular studies it is known that the IP 3R in Drosophila is activated by G-protein coupled receptors (GPCRs). However, GPCRs that act upstream of the IP 3R in the context of flight are not known. Therefore, we performed a genetic RNAi screen to identify GPCRs which regulate flight. This screen was followed by a secondary suppressor screen that assessed the role of each identified GPCR in activating IP 3/Ca 2+ signaling. We found 5 such GPCRs. Our results demonstrate that these GPCRs are required during flight circuit development and during adult flight. One flight-regulating receptor identified was the Pigment Dispersing Factor Receptor (PdfR). This receptor is known to regulate behaviors such as circadian rhythms, geotaxis and reproduction. A spatio-temporal analysis of PdfR flight function indicates that it regulates both flight circuit development and acute flight through multiple neurons. We postulate that PdfR signaling could modulate and integrate multiple behavioral inputs in Drosophila and other flying insects.

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          Most cited references51

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          STIM is a Ca2+ sensor essential for Ca2+-store-depletion-triggered Ca2+ influx.

          Ca(2+) signaling in nonexcitable cells is typically initiated by receptor-triggered production of inositol-1,4,5-trisphosphate and the release of Ca(2+) from intracellular stores. An elusive signaling process senses the Ca(2+) store depletion and triggers the opening of plasma membrane Ca(2+) channels. The resulting sustained Ca(2+) signals are required for many physiological responses, such as T cell activation and differentiation. Here, we monitored receptor-triggered Ca(2+) signals in cells transfected with siRNAs against 2,304 human signaling proteins, and we identified two proteins required for Ca(2+)-store-depletion-mediated Ca(2+) influx, STIM1 and STIM2. These proteins have a single transmembrane region with a putative Ca(2+) binding domain in the lumen of the endoplasmic reticulum. Ca(2+) store depletion led to a rapid translocation of STIM1 into puncta that accumulated near the plasma membrane. Introducing a point mutation in the STIM1 Ca(2+) binding domain resulted in prelocalization of the protein in puncta, and this mutant failed to respond to store depletion. Our study suggests that STIM proteins function as Ca(2+) store sensors in the signaling pathway connecting Ca(2+) store depletion to Ca(2+) influx.
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            STIM1 is a Ca2+ sensor that activates CRAC channels and migrates from the Ca2+ store to the plasma membrane.

            As the sole Ca2+ entry mechanism in a variety of non-excitable cells, store-operated calcium (SOC) influx is important in Ca2+ signalling and many other cellular processes. A calcium-release-activated calcium (CRAC) channel in T lymphocytes is the best-characterized SOC influx channel and is essential to the immune response, sustained activity of CRAC channels being required for gene expression and proliferation. The molecular identity and the gating mechanism of SOC and CRAC channels have remained elusive. Previously we identified Stim and the mammalian homologue STIM1 as essential components of CRAC channel activation in Drosophila S2 cells and human T lymphocytes. Here we show that the expression of EF-hand mutants of Stim or STIM1 activates CRAC channels constitutively without changing Ca2+ store content. By immunofluorescence, EM localization and surface biotinylation we show that STIM1 migrates from endoplasmic-reticulum-like sites to the plasma membrane upon depletion of the Ca2+ store. We propose that STIM1 functions as the missing link between Ca2+ store depletion and SOC influx, serving as a Ca2+ sensor that translocates upon store depletion to the plasma membrane to activate CRAC channels.
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              A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in Drosophila.

              The mechanisms by which circadian pacemaker systems transmit timing information to control behavior are largely unknown. Here, we define two critical features of that mechanism in Drosophila. We first describe animals mutant for the pdf neuropeptide gene, which is expressed by most of the candidate pacemakers (LNv neurons). Next, we describe animals in which pdf neurons were selectively ablated. Both sets of animals produced similar behavioral phenotypes. Both sets entrained to light, but both were largely arrhythmic under constant conditions. A minority of each pdf variant exhibited weak to moderate free-running rhythmicity. These results confirm the assignment of LNv neurons as the principal circadian pacemakers controlling daily locomotion in Drosophila. They also implicate PDF as the principal circadian transmitter.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                October 2013
                October 2013
                3 October 2013
                : 9
                : 10
                : e1003849
                Affiliations
                [1]National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, India
                Washington University Medical School, United States of America
                Author notes

                The authors have declared that no competing interests exist.

                Conceived and designed the experiments: TA GH. Performed the experiments: TA SS. Analyzed the data: TA SS GH. Contributed reagents/materials/analysis tools: GH. Wrote the paper: TA SS GH. Edited the paper: TA SS GH.

                Article
                PGENETICS-D-13-01291
                10.1371/journal.pgen.1003849
                3789835
                24098151
                72209b9d-e7fe-4cf6-ada0-9c5a84781e42
                Copyright @ 2013

                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 credited.

                History
                : 17 May 2013
                : 18 August 2013
                Page count
                Pages: 14
                Funding
                This work was supported by a research fellowship from the National Centre for Biological Sciences, Tata Institute of Fundamental Research ( http://www.ncbs.res.in) to TA and from the Council of Scientific and Industrial Research ( http://rdpp.csir.res.in/csir_acsir/Home.aspx) to SS. The project was supported financially by core funds from the National Centre for Biological Sciences, Tata Institute of Fundamental Research ( http://www.ncbs.res.in) to GH. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article

                Genetics
                Genetics

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