RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides
Locomotor activity rhythms are controlled by a network of ~150 circadian neurons within the adult Drosophila brain. They are subdivided based on their anatomical locations and properties. We profiled transcripts "around the clock" from three key groups of circadian neurons with different f...
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description | Locomotor activity rhythms are controlled by a network of ~150 circadian neurons within the adult Drosophila brain. They are subdivided based on their anatomical locations and properties. We profiled transcripts "around the clock" from three key groups of circadian neurons with different functions. We also profiled a non-circadian outgroup, dopaminergic (TH) neurons. They have cycling transcripts but fewer than clock neurons as well as low expression and poor cycling of clock gene transcripts. This suggests that TH neurons do not have a canonical circadian clock and that their gene expression cycling is driven by brain systemic cues. The three circadian groups are surprisingly diverse in their cycling transcripts and overall gene expression patterns, which include known and putative novel neuropeptides. Even the overall phase distributions of cycling transcripts are distinct, indicating that different regulatory principles govern transcript oscillations. This surprising cell-type diversity parallels the functional heterogeneity of the different neurons. |
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They are subdivided based on their anatomical locations and properties. We profiled transcripts "around the clock" from three key groups of circadian neurons with different functions. We also profiled a non-circadian outgroup, dopaminergic (TH) neurons. They have cycling transcripts but fewer than clock neurons as well as low expression and poor cycling of clock gene transcripts. This suggests that TH neurons do not have a canonical circadian clock and that their gene expression cycling is driven by brain systemic cues. The three circadian groups are surprisingly diverse in their cycling transcripts and overall gene expression patterns, which include known and putative novel neuropeptides. Even the overall phase distributions of cycling transcripts are distinct, indicating that different regulatory principles govern transcript oscillations. This surprising cell-type diversity parallels the functional heterogeneity of the different neurons.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1006613</identifier><identifier>PMID: 28182648</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animals ; Animals, Genetically Modified ; Behavior ; Biology ; Biology and Life Sciences ; Brain ; Brain - cytology ; Brain - metabolism ; Circadian Clocks - genetics ; Circadian rhythm ; Dopaminergic Neurons - metabolism ; Drosophila ; Drosophila melanogaster - cytology ; Drosophila melanogaster - genetics ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Feedback ; Funding ; Gene expression ; Gene Expression Profiling - methods ; Genetic aspects ; Genomics ; Insects ; Microscopy, Fluorescence ; Neurons ; Neurons - metabolism ; Neuropeptides ; Neuropeptides - genetics ; Neurosciences ; Oligonucleotide Array Sequence Analysis ; Research and Analysis Methods ; RNA sequencing ; Rodents ; Sequence Analysis, RNA - methods ; Sleep ; Time Factors ; Transcription factors ; Transcription Factors - genetics</subject><ispartof>PLoS genetics, 2017-02, Vol.13 (2), p.e1006613-e1006613</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Public Library of Science. 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: clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides. PLoS Genet 13(2): e1006613. doi:10.1371/journal.pgen.1006613</rights><rights>2017 Abruzzi et al 2017 Abruzzi et al</rights><rights>2017 Public Library of Science. 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: clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides. 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cytology</topic><topic>Brain - metabolism</topic><topic>Circadian Clocks - genetics</topic><topic>Circadian rhythm</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - cytology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Feedback</topic><topic>Funding</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Genetic aspects</topic><topic>Genomics</topic><topic>Insects</topic><topic>Microscopy, Fluorescence</topic><topic>Neurons</topic><topic>Neurons - metabolism</topic><topic>Neuropeptides</topic><topic>Neuropeptides - genetics</topic><topic>Neurosciences</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Research and Analysis Methods</topic><topic>RNA sequencing</topic><topic>Rodents</topic><topic>Sequence Analysis, RNA - methods</topic><topic>Sleep</topic><topic>Time Factors</topic><topic>Transcription factors</topic><topic>Transcription Factors - 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They are subdivided based on their anatomical locations and properties. We profiled transcripts "around the clock" from three key groups of circadian neurons with different functions. We also profiled a non-circadian outgroup, dopaminergic (TH) neurons. They have cycling transcripts but fewer than clock neurons as well as low expression and poor cycling of clock gene transcripts. This suggests that TH neurons do not have a canonical circadian clock and that their gene expression cycling is driven by brain systemic cues. The three circadian groups are surprisingly diverse in their cycling transcripts and overall gene expression patterns, which include known and putative novel neuropeptides. Even the overall phase distributions of cycling transcripts are distinct, indicating that different regulatory principles govern transcript oscillations. 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subjects | Analysis Animals Animals, Genetically Modified Behavior Biology Biology and Life Sciences Brain Brain - cytology Brain - metabolism Circadian Clocks - genetics Circadian rhythm Dopaminergic Neurons - metabolism Drosophila Drosophila melanogaster - cytology Drosophila melanogaster - genetics Drosophila melanogaster - metabolism Drosophila Proteins - genetics Feedback Funding Gene expression Gene Expression Profiling - methods Genetic aspects Genomics Insects Microscopy, Fluorescence Neurons Neurons - metabolism Neuropeptides Neuropeptides - genetics Neurosciences Oligonucleotide Array Sequence Analysis Research and Analysis Methods RNA sequencing Rodents Sequence Analysis, RNA - methods Sleep Time Factors Transcription factors Transcription Factors - genetics |
title | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
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