• Wiley Online Library will be disrupted on 26 May from 10:00-12:00 BST (05:00-07:00 EDT) for essential maintenance

Central and Peripheral Circadian Oscillators in Drosophila

  1. Derek J. Chadwick Organizer,
  2. Jamie A. Goode
  1. Paul E. Hardin1,
  2. Balaji Krishnan2,
  3. Jerry H. Houl2,
  4. Hao Zheng2,
  5. Fanny S. Ng2,
  6. Stuart E. Dryer2,
  7. Nick R. J. Glossop2

Published Online: 7 OCT 2008

DOI: 10.1002/0470090839.ch11

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

How to Cite

Hardin, P. E., Krishnan, B., Houl, J. H., Zheng, H., Ng, F. S., Dryer, S. E. and Glossop, N. R. J. (2008) Central and Peripheral Circadian Oscillators in Drosophila, in Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253 (eds D. J. Chadwick and J. A. Goode), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470090839.ch11

Author Information

  1. 1

    Department of Biology and Biochemistry, University of Houston, 369 Science and Research Building 2, Houston, TX 77204-5001, USA

  2. 2

    Department of Biology and Biochemistry, University of Houston, Houston, TX 771204-5001, USA

Publication History

  1. Published Online: 7 OCT 2008
  2. Published Print: 28 OCT 2003

Book Series:

  1. Novartis Foundation Symposia

Book Series Editors:

  1. Novartis Foundation

ISBN Information

Print ISBN: 9780470852835

Online ISBN: 9780470090831

SEARCH

Summary

Drosophila circadian oscillators comprise interlocked period (per)/timeless (tim) and Clock (Clk) transcriptional/translational feedback loops. Within these feedback loops, CLOCK (CLK) and CYCLE (CYC) bind E-box elements to activate per and tim transcription, and we now show that at the same time CLK–CYC repress Clk by activating the transcriptional repressor vrille (vri), thus accounting for the opposite cycling phases of these transcripts and identifying vri as the negative component of the Clk-feedback-loop. The core oscillator mechanism is assumed to be the same for oscillators in different tissues. However, we have shown that CRYPTOCHROME (CRY) has a light-independent function in the oscillator that controls olfaction rhythms, suggesting that CRY may function within the oscillator mechanism itself as it does in mammals. These olfaction rhythms require the function of ‘peripheral’ oscillators which are distinct from the ‘central’ lateral neuron (LN) oscillators that mediate locomotor activity rhythms. Preliminary results show that antennal oscillator cells are sufficient and LNs are not necessary for olfaction rhythms, indicating that unlike the situation in mammals, the central oscillator has little impact on the olfaction rhythm oscillator under these conditions.