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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 functions....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325595/ https://www.ncbi.nlm.nih.gov/pubmed/28182648 http://dx.doi.org/10.1371/journal.pgen.1006613 |
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author | Abruzzi, Katharine C. Zadina, Abigail Luo, Weifei Wiyanto, Evelyn Rahman, Reazur Guo, Fang Shafer, Orie Rosbash, Michael |
author_facet | Abruzzi, Katharine C. Zadina, Abigail Luo, Weifei Wiyanto, Evelyn Rahman, Reazur Guo, Fang Shafer, Orie Rosbash, Michael |
author_sort | Abruzzi, Katharine C. |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-5325595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53255952017-03-10 RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides Abruzzi, Katharine C. Zadina, Abigail Luo, Weifei Wiyanto, Evelyn Rahman, Reazur Guo, Fang Shafer, Orie Rosbash, Michael PLoS Genet Research Article 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. Public Library of Science 2017-02-09 /pmc/articles/PMC5325595/ /pubmed/28182648 http://dx.doi.org/10.1371/journal.pgen.1006613 Text en © 2017 Abruzzi 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Abruzzi, Katharine C. Zadina, Abigail Luo, Weifei Wiyanto, Evelyn Rahman, Reazur Guo, Fang Shafer, Orie Rosbash, Michael RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title_full | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title_fullStr | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title_full_unstemmed | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title_short | RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
title_sort | rna-seq analysis of drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325595/ https://www.ncbi.nlm.nih.gov/pubmed/28182648 http://dx.doi.org/10.1371/journal.pgen.1006613 |
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