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. 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 (LNvs), is essential for self-sustained behavioral rhythms and has been proposed to be the primary pacemaker for locomotor activity rhythms. With an LNv-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 LNv-specific neuropeptide, because the molecular oscillations are gradually lost when Pdf01 mutant flies are exposed to free-running conditions. This observation precisely parallels the previously reported effect on behavioral rhythms of the Pdf01 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 LNvs 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 LNvs alone are insufficient to support the circadian program. Based on the damping results with Pdf01 mutant flies, we propose that LNvs, 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.

[1]  N. Turner PLOS Biology , 2004, BMJ : British Medical Journal.

[2]  R. Allada,et al.  A recessive mutant of Drosophila Clock reveals a role in circadian rhythm amplitude , 2003, The EMBO journal.

[3]  Kevin P. Keegan,et al.  Drosophila Clock Can Generate Ectopic Circadian Clocks , 2003, Cell.

[4]  S. Yamaguchi,et al.  Suprachiasmatic Nucleus Grafts Restore Circadian Behavioral Rhythms of Genetically Arrhythmic Mice , 2003, Current Biology.

[5]  A. Sehgal,et al.  Circadian Control of Eclosion Interaction between a Central and Peripheral Clock in Drosophila melanogaster , 2003, Current Biology.

[6]  Jeffrey C. Hall,et al.  Genetics and molecular biology of rhythms in Drosophila and other insects. , 2003, Advances in genetics.

[7]  Michael W. Young,et al.  vrille, Pdp1, and dClock Form a Second Feedback Loop in the Drosophila Circadian Clock , 2003, Cell.

[8]  Scott M. Dudek,et al.  VRILLE Feeds Back to Control Circadian Transcription of Clock in the Drosophila Circadian Oscillator , 2003, Neuron.

[9]  Paolo Sassone-Corsi,et al.  A Web of Circadian Pacemakers , 2002, Cell.

[10]  P. Hardin,et al.  Central and peripheral circadian oscillator mechanisms in flies and mammals. , 2002, Journal of cell science.

[11]  J. Truman,et al.  Sequential Nuclear Accumulation of the Clock Proteins Period and Timeless in the Pacemaker Neurons of Drosophila melanogaster , 2002, The Journal of Neuroscience.

[12]  K. White,et al.  Identification of genes involved in Drosophila melanogaster geotaxis, a complex behavioral trait , 2002, Nature Genetics.

[13]  Michael N Nitabach,et al.  Electrical Silencing of Drosophila Pacemaker Neurons Stops the Free-Running Circadian Clock , 2002, Cell.

[14]  E. Maywood,et al.  The VPAC2 Receptor Is Essential for Circadian Function in the Mouse Suprachiasmatic Nuclei , 2002, Cell.

[15]  Satchidananda Panda,et al.  Circadian rhythms from flies to human , 2002, Nature.

[16]  Jeffrey C. Hall,et al.  Advanced analysis of a cryptochrome mutation's effects on the robustness and phase of molecular cycles in isolated peripheral tissues of Drosophila , 2002, BMC Neuroscience.

[17]  Joel D Levine,et al.  Signal analysis of behavioral and molecular cycles , 2002, BMC Neuroscience.

[18]  Jeffrey C. Hall,et al.  A new role for cryptochrome in a Drosophila circadian oscillator , 2001, Nature.

[19]  A. Sehgal,et al.  Role of Molecular Oscillations in Generating Behavioral Rhythms in Drosophila , 2001, Neuron.

[20]  Jeffrey C. Hall,et al.  Neuroanatomy of cells expressing clock genes in Drosophila: Transgenic manipulation of the period and timeless genes to mark the perikarya of circadian pacemaker neurons and their projections , 2000, The Journal of comparative neurology.

[21]  Jeffrey C. Hall,et al.  Drosophila CRY Is a Deep Brain Circadian Photoreceptor , 2000, Neuron.

[22]  C. Helfrich-Förster,et al.  Ectopic Expression of the Neuropeptide Pigment-Dispersing Factor Alters Behavioral Rhythms in Drosophila melanogaster , 2000, The Journal of Neuroscience.

[23]  Jeffrey C. Hall,et al.  A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in Drosophila. , 2000, Cell.

[24]  J. C. Hall,et al.  Differential regulation of circadian pacemaker output by separate clock genes in Drosophila. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Paul E. Hardin,et al.  dCLOCK Is Present in Limiting Amounts and Likely Mediates Daily Interactions between the dCLOCK–CYC Transcription Factor and the PER–TIM Complex , 2000, The Journal of Neuroscience.

[26]  Jeffrey C. Hall,et al.  Transplanted Drosophila excretory tubules maintain circadian clock cycling out of phase with the host , 2000, Current Biology.

[27]  P. Hardin,et al.  Interlocked feedback loops within the Drosophila circadian oscillator. , 1999, Science.

[28]  J. Dunlap Molecular Bases for Circadian Clocks , 1999, Cell.

[29]  Jeffrey C. Hall,et al.  The cryb Mutation Identifies Cryptochrome as a Circadian Photoreceptor in Drosophila , 1998, Cell.

[30]  Jeffrey C. Hall,et al.  CRY, a Drosophila Clock and Light-Regulated Cryptochrome, Is a Major Contributor to Circadian Rhythm Resetting and Photosensitivity , 1998, Cell.

[31]  U. Schibler,et al.  A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells , 1998, Cell.

[32]  Jeffrey C. Hall,et al.  CYCLE Is a Second bHLH-PAS Clock Protein Essential for Circadian Rhythmicity and Transcription of Drosophila period and timeless , 1998, Cell.

[33]  Jeffrey C. Hall,et al.  A Mutant Drosophila Homolog of Mammalian Clock Disrupts Circadian Rhythms and Transcription of period and timeless , 1998, Cell.

[34]  C. Helfrich-Förster Robust circadian rhythmicity of Drosophila melanogaster requires the presence of lateral neurons: a brain-behavioral study of disconnected mutants , 1998, Journal of Comparative Physiology A.

[35]  S. Kay,et al.  Independent photoreceptive circadian clocks throughout Drosophila. , 1997, Science.

[36]  Jeffrey C. Hall,et al.  Multiple circadian‐regulated elements contribute to cycling period gene expression in Drosophila , 1997, The EMBO journal.

[37]  B. Petri,et al.  Pigment-Dispersing Hormone Shifts the Phase of the Circadian Pacemaker of the Cockroach Leucophaea maderae , 1997, The Journal of Neuroscience.

[38]  Hongkui Zeng,et al.  Effect of constant light and circadian entrainment of perS flies: evidence for light‐mediated delay of the negative feedback loop in Drosophila. , 1996, The EMBO journal.

[39]  C. Helfrich-Förster The period clock gene is expressed in central nervous system neurons which also produce a neuropeptide that reveals the projections of circadian pacemaker cells within the brain of Drosophila melanogaster. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[40]  P. Hardin Analysis of period mRNA cycling in Drosophila head and body tissues indicates that body oscillators behave differently from head oscillators , 1994, Molecular and cellular biology.

[41]  A. Sehgal,et al.  Loss of circadian behavioral rhythms and per RNA oscillations in the Drosophila mutant timeless. , 1994, Science.

[42]  J. P. Riehm,et al.  Pigment‐Dispersing Hormones a , 1993, Annals of the New York Academy of Sciences.

[43]  P. Hardin,et al.  Behavioral and molecular analyses suggest that circadian output is disrupted by disconnected mutants in D. melanogaster. , 1992, The EMBO journal.

[44]  J. Takahashi,et al.  Stopping time: the genetics of fly and mouse circadian clocks. , 2001, Annual review of neuroscience.

[45]  J. C. Hall,et al.  Circadian and ultradian rhythms inperiod mutants ofDrosophila melanogaster , 1987, Behavior genetics.