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dc.contributor.authorZhang, Yong
dc.contributor.authorEmery, Patrick
dc.date2022-08-11T08:08:18.000
dc.date.accessioned2022-08-23T15:50:52Z
dc.date.available2022-08-23T15:50:52Z
dc.date.issued2013-04-10
dc.date.submitted2013-07-02
dc.identifier.citationNeuron. 2013 Apr 10;78(1):152-65. doi: 10.1016/j.neuron.2013.01.035. <a href="http://dx.doi.org/10.1016/j.neuron.2013.01.035">Link to article on publisher's site</a>
dc.identifier.issn0896-6273 (Linking)
dc.identifier.doi10.1016/j.neuron.2013.01.035
dc.identifier.pmid23583112
dc.identifier.urihttp://hdl.handle.net/20.500.14038/28758
dc.description.abstractThe neuropeptide PDF is crucial for Drosophila circadian behavior: it keeps circadian neurons synchronized. Here, we identify GW182 as a key regulator of PDF signaling. Indeed, GW182 downregulation results in phenotypes similar to those of Pdf and Pdf-receptor (Pdfr) mutants. gw182 genetically interacts with Pdfr and cAMP signaling, which is essential for PDFR function. GW182 mediates miRNA-dependent gene silencing through its interaction with AGO1. Consistently, GW182's AGO1 interaction domain is required for GW182's circadian function. Moreover, our results indicate that GW182 modulates PDFR signaling by silencing the expression of the cAMP phosphodiesterase DUNCE. Importantly, this repression is under photic control, and GW182 activity level--which is limiting in circadian neurons--influences the responses of the circadian neural network to light. We propose that GW182's gene silencing activity functions as a rheostat for PDFR signaling and thus profoundly impacts the circadian neural network and its response to environmental inputs.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23583112&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.neuron.2013.01.035
dc.subjectAnimals
dc.subjectAnimals, Genetically Modified
dc.subjectCircadian Rhythm
dc.subjectDrosophila
dc.subjectDrosophila Proteins
dc.subjectGene Expression Regulation, Developmental
dc.subjectGreen Fluorescent Proteins
dc.subjectLocomotion
dc.subjectMale
dc.subjectMicroRNAs
dc.subjectRNA Interference
dc.subjectReceptors, G-Protein-Coupled
dc.subjectSignal Transduction
dc.subjectTemperature
dc.subjectTranscription Factors
dc.subjectMolecular and Cellular Neuroscience
dc.subjectNeuroscience and Neurobiology
dc.titleGW182 controls Drosophila circadian behavior and PDF-receptor signaling
dc.typeJournal Article
dc.source.journaltitleNeuron
dc.source.volume78
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/100
dc.identifier.contextkey4276315
html.description.abstract<p>The neuropeptide PDF is crucial for Drosophila circadian behavior: it keeps circadian neurons synchronized. Here, we identify GW182 as a key regulator of PDF signaling. Indeed, GW182 downregulation results in phenotypes similar to those of Pdf and Pdf-receptor (Pdfr) mutants. gw182 genetically interacts with Pdfr and cAMP signaling, which is essential for PDFR function. GW182 mediates miRNA-dependent gene silencing through its interaction with AGO1. Consistently, GW182's AGO1 interaction domain is required for GW182's circadian function. Moreover, our results indicate that GW182 modulates PDFR signaling by silencing the expression of the cAMP phosphodiesterase DUNCE. Importantly, this repression is under photic control, and GW182 activity level--which is limiting in circadian neurons--influences the responses of the circadian neural network to light. We propose that GW182's gene silencing activity functions as a rheostat for PDFR signaling and thus profoundly impacts the circadian neural network and its response to environmental inputs.</p>
dc.identifier.submissionpathfaculty_pubs/100
dc.contributor.departmentEmery Lab
dc.contributor.departmentNeurobiology
dc.source.pages152-65


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