Cargando…
Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock
Circadian locomotor behaviour is controlled by a pacemaker circuit composed of clock-containing neurons. To interrogate the mechanistic relationship between the molecular clockwork and network communication critical to the operation of the Drosophila circadian pacemaker circuit, we established new f...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278502/ https://www.ncbi.nlm.nih.gov/pubmed/28134281 http://dx.doi.org/10.1038/srep41560 |
_version_ | 1782502652913909760 |
---|---|
author | Sabado, Virginie Vienne, Ludovic Nunes, José Manuel Rosbash, Michael Nagoshi, Emi |
author_facet | Sabado, Virginie Vienne, Ludovic Nunes, José Manuel Rosbash, Michael Nagoshi, Emi |
author_sort | Sabado, Virginie |
collection | PubMed |
description | Circadian locomotor behaviour is controlled by a pacemaker circuit composed of clock-containing neurons. To interrogate the mechanistic relationship between the molecular clockwork and network communication critical to the operation of the Drosophila circadian pacemaker circuit, we established new fluorescent circadian reporters that permit single-cell recording of transcriptional and post-transcriptional rhythms in brain explants and cultured neurons. Live-imaging experiments combined with pharmacological and genetic manipulations demonstrate that the neuropeptide pigment-dispersing factor (PDF) amplifies the molecular rhythms via time-of-day- and activity-dependent upregulation of transcription from E-box-containing clock gene promoters within key pacemaker neurons. The effect of PDF on clock gene transcription and the known role of PDF in enhancing PER/TIM stability occur via independent pathways downstream of the PDF receptor, the former through a cAMP-independent mechanism and the latter through a cAMP-PKA dependent mechanism. These results confirm and extend the mechanistic understanding of the role of PDF in controlling the synchrony of the pacemaker neurons. More broadly, our results establish the utility of the new live-imaging tools for the study of molecular-neural interactions important for the operation of the circadian pacemaker circuit. |
format | Online Article Text |
id | pubmed-5278502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52785022017-02-03 Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock Sabado, Virginie Vienne, Ludovic Nunes, José Manuel Rosbash, Michael Nagoshi, Emi Sci Rep Article Circadian locomotor behaviour is controlled by a pacemaker circuit composed of clock-containing neurons. To interrogate the mechanistic relationship between the molecular clockwork and network communication critical to the operation of the Drosophila circadian pacemaker circuit, we established new fluorescent circadian reporters that permit single-cell recording of transcriptional and post-transcriptional rhythms in brain explants and cultured neurons. Live-imaging experiments combined with pharmacological and genetic manipulations demonstrate that the neuropeptide pigment-dispersing factor (PDF) amplifies the molecular rhythms via time-of-day- and activity-dependent upregulation of transcription from E-box-containing clock gene promoters within key pacemaker neurons. The effect of PDF on clock gene transcription and the known role of PDF in enhancing PER/TIM stability occur via independent pathways downstream of the PDF receptor, the former through a cAMP-independent mechanism and the latter through a cAMP-PKA dependent mechanism. These results confirm and extend the mechanistic understanding of the role of PDF in controlling the synchrony of the pacemaker neurons. More broadly, our results establish the utility of the new live-imaging tools for the study of molecular-neural interactions important for the operation of the circadian pacemaker circuit. Nature Publishing Group 2017-01-30 /pmc/articles/PMC5278502/ /pubmed/28134281 http://dx.doi.org/10.1038/srep41560 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sabado, Virginie Vienne, Ludovic Nunes, José Manuel Rosbash, Michael Nagoshi, Emi Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title | Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title_full | Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title_fullStr | Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title_full_unstemmed | Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title_short | Fluorescence circadian imaging reveals a PDF-dependent transcriptional regulation of the Drosophila molecular clock |
title_sort | fluorescence circadian imaging reveals a pdf-dependent transcriptional regulation of the drosophila molecular clock |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278502/ https://www.ncbi.nlm.nih.gov/pubmed/28134281 http://dx.doi.org/10.1038/srep41560 |
work_keys_str_mv | AT sabadovirginie fluorescencecircadianimagingrevealsapdfdependenttranscriptionalregulationofthedrosophilamolecularclock AT vienneludovic fluorescencecircadianimagingrevealsapdfdependenttranscriptionalregulationofthedrosophilamolecularclock AT nunesjosemanuel fluorescencecircadianimagingrevealsapdfdependenttranscriptionalregulationofthedrosophilamolecularclock AT rosbashmichael fluorescencecircadianimagingrevealsapdfdependenttranscriptionalregulationofthedrosophilamolecularclock AT nagoshiemi fluorescencecircadianimagingrevealsapdfdependenttranscriptionalregulationofthedrosophilamolecularclock |