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Drosophila Free-Running Rhythms Require Intercellular Communication

Robust self-sustained oscillations are a ubiquitous characteristic of circadian rhythms. These include Drosophila locomotor activity rhythms, which persist for weeks in constant darkness (DD). Yet the molecular oscillations that underlie circadian rhythms damp rapidly in many Drosophila tissues. Alt...

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Detalles Bibliográficos
Autores principales: Peng, Ying, Stoleru, Dan, Levine, Joel D, Hall, Jeffrey C, Rosbash, Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC193604/
https://www.ncbi.nlm.nih.gov/pubmed/12975658
http://dx.doi.org/10.1371/journal.pbio.0000013
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author Peng, Ying
Stoleru, Dan
Levine, Joel D
Hall, Jeffrey C
Rosbash, Michael
author_facet Peng, Ying
Stoleru, Dan
Levine, Joel D
Hall, Jeffrey C
Rosbash, Michael
author_sort Peng, Ying
collection PubMed
description Robust self-sustained oscillations are a ubiquitous characteristic of circadian rhythms. These include Drosophila locomotor activity rhythms, which persist for weeks in constant darkness (DD). Yet the molecular oscillations that underlie circadian rhythms damp rapidly in many Drosophila tissues. Although much progress has been made in understanding the biochemical and cellular basis of circadian rhythms, the mechanisms that underlie the differences between damped and self-sustaining oscillations remain largely unknown. A small cluster of neurons in adult Drosophila brain, the ventral lateral neurons (LN(v)s), is essential for self-sustained behavioral rhythms and has been proposed to be the primary pacemaker for locomotor activity rhythms. With an LN(v)-specific driver, we restricted functional clocks to these neurons and showed that they are not sufficient to drive circadian locomotor activity rhythms. Also contrary to expectation, we found that all brain clock neurons manifest robust circadian oscillations of timeless and cryptochrome RNA for many days in DD. This persistent molecular rhythm requires pigment-dispersing factor (PDF), an LN(v)-specific neuropeptide, because the molecular oscillations are gradually lost when Pdf(01) mutant flies are exposed to free-running conditions. This observation precisely parallels the previously reported effect on behavioral rhythms of the Pdf(01) mutant. PDF is likely to affect some clock neurons directly, since the peptide appears to bind to the surface of many clock neurons, including the LN(v)s themselves. We showed that the brain circadian clock in Drosophila is clearly distinguishable from the eyes and other rapidly damping peripheral tissues, as it sustains robust molecular oscillations in DD. At the same time, different clock neurons are likely to work cooperatively within the brain, because the LN(v)s alone are insufficient to support the circadian program. Based on the damping results with Pdf(01) mutant flies, we propose that LN(v)s, and specifically the PDF neuropeptide that it synthesizes, are important in coordinating a circadian cellular network within the brain. The cooperative function of this network appears to be necessary for maintaining robust molecular oscillations in DD and is the basis of sustained circadian locomotor activity rhythms.
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spelling pubmed-1936042003-09-16 Drosophila Free-Running Rhythms Require Intercellular Communication Peng, Ying Stoleru, Dan Levine, Joel D Hall, Jeffrey C Rosbash, Michael PLoS Biol Research Article Robust self-sustained oscillations are a ubiquitous characteristic of circadian rhythms. These include Drosophila locomotor activity rhythms, which persist for weeks in constant darkness (DD). Yet the molecular oscillations that underlie circadian rhythms damp rapidly in many Drosophila tissues. Although much progress has been made in understanding the biochemical and cellular basis of circadian rhythms, the mechanisms that underlie the differences between damped and self-sustaining oscillations remain largely unknown. A small cluster of neurons in adult Drosophila brain, the ventral lateral neurons (LN(v)s), is essential for self-sustained behavioral rhythms and has been proposed to be the primary pacemaker for locomotor activity rhythms. With an LN(v)-specific driver, we restricted functional clocks to these neurons and showed that they are not sufficient to drive circadian locomotor activity rhythms. Also contrary to expectation, we found that all brain clock neurons manifest robust circadian oscillations of timeless and cryptochrome RNA for many days in DD. This persistent molecular rhythm requires pigment-dispersing factor (PDF), an LN(v)-specific neuropeptide, because the molecular oscillations are gradually lost when Pdf(01) mutant flies are exposed to free-running conditions. This observation precisely parallels the previously reported effect on behavioral rhythms of the Pdf(01) mutant. PDF is likely to affect some clock neurons directly, since the peptide appears to bind to the surface of many clock neurons, including the LN(v)s themselves. We showed that the brain circadian clock in Drosophila is clearly distinguishable from the eyes and other rapidly damping peripheral tissues, as it sustains robust molecular oscillations in DD. At the same time, different clock neurons are likely to work cooperatively within the brain, because the LN(v)s alone are insufficient to support the circadian program. Based on the damping results with Pdf(01) mutant flies, we propose that LN(v)s, and specifically the PDF neuropeptide that it synthesizes, are important in coordinating a circadian cellular network within the brain. The cooperative function of this network appears to be necessary for maintaining robust molecular oscillations in DD and is the basis of sustained circadian locomotor activity rhythms. Public Library of Science 2003-10 2003-09-15 /pmc/articles/PMC193604/ /pubmed/12975658 http://dx.doi.org/10.1371/journal.pbio.0000013 Text en Copyright: ©2003 Peng 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Peng, Ying
Stoleru, Dan
Levine, Joel D
Hall, Jeffrey C
Rosbash, Michael
Drosophila Free-Running Rhythms Require Intercellular Communication
title Drosophila Free-Running Rhythms Require Intercellular Communication
title_full Drosophila Free-Running Rhythms Require Intercellular Communication
title_fullStr Drosophila Free-Running Rhythms Require Intercellular Communication
title_full_unstemmed Drosophila Free-Running Rhythms Require Intercellular Communication
title_short Drosophila Free-Running Rhythms Require Intercellular Communication
title_sort drosophila free-running rhythms require intercellular communication
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC193604/
https://www.ncbi.nlm.nih.gov/pubmed/12975658
http://dx.doi.org/10.1371/journal.pbio.0000013
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