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Circadian Transcriptional Output in the SCN and Liver of the Mouse

  1. Derek J. Chadwick Organizer,
  2. Jamie A. Goode
  1. John B. Hogenesch1,
  2. Satchidananda Panda1,
  3. Steve Kay2,
  4. Joseph S. Takahashi3,*

Published Online: 7 OCT 2008

DOI: 10.1002/0470090839.ch13

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

How to Cite

Hogenesch, J. B., Panda, S., Kay, S. and Takahashi, J. S. (2008) Circadian Transcriptional Output in the SCN and Liver of the Mouse, 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.ch13

Author Information

  1. 1

    The Genomics Institute of the Novartis Research Foundation, San Diego, CA, 9212, USA

  2. 2

    Department of Cell Biology, The Scripps Research Institute, La Jolla, CA, 92037, USA

  3. 3

    Howard Hughes Medical Institute, Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208, USA

*Howard Hughes Medical Institute, Department of Neurobiology & Physiology, Northwestern University, 2153 North Campus Drive, Evanston, IL 60208, 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

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Summary

Circadian oscillators orchestrate daily rhythms in behaviour and physiology to adapt to the predictable daily appearance of light. Identifying the complement of circadian-regulated transcripts in major organs is critical in the understanding of both the biochemical targets of clock regulation and the mechanism of such control. Recent analysis of temporal gene expression patterns in peripheral and central oscillators have revealed hundreds of circadian-regulated transcripts, most of which are tissue-specific. Mapping of these transcripts to physiological processes and pathways has revealed that major functions of those organs tested are under circadian regulation, and importantly, key and rate-limiting steps in these processes are often the targets of circadian control. Overall, nearly 10% of the mammalian genome may be regulated by the clock, demonstrating the pervasive control of the circadian oscillator in temporal coordination of transcription throughout the organism. This wealth of circadian outputs offers exciting challenges to deciphering systems-level transcriptional regulatory mechanisms that underlie spatiotemporal gene expression.