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CK1 and GSK3 in the Drosophila and Mammalian Circadian Clock

  1. Derek J. Chadwick Organizer,
  2. Jamie A. Goode
  1. Emily Harms,
  2. Michael W. Young*,
  3. Lino Saez

Published Online: 7 OCT 2008

DOI: 10.1002/0470090839.ch19

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

Molecular Clocks and Light Signalling: Novartis Foundation Symposium 253

How to Cite

Harms, E., Young, M. W. and Saez, L. (2008) CK1 and GSK3 in the Drosophila and Mammalian Circadian Clock, 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.ch19

Author Information

  1. Laboratory of Genetics, The Rockefeller University, 1230 York Avenue, Box 288, New York, NY 10021, USA

*Laboratory of Genetics, The Rockefeller University, 1230 York Avenue, Box 288, New York, NY 10021, 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

Two kinases, DOUBLETIME and SHAGGY, have been shown to play a role in the circadian clock. DOUBLETIME, the Drosophila orthologue of casein kinase 1, can phosphorylate PERIOD in the cytoplasm and in the nucleus. This phosphorylation destabilizes PERIOD in both locations and sets patterns of both cytoplasmic accumulation and nuclear turnover. Cytoplasmic phosphorylation postpones accumulation of PERIOD and affects timing of nuclear accumulation of PERIOD/TIMELESS complexes. SHAGGY, the Drosophila orthologue of glycogen synthase kinase 3, phosphorylates TIMELESS and promotes nuclear translocation of PERIOD/TIMELESS complexes. Thus, the opposing effects of these two kinases in the cytoplasm are crucial for establishing the ∼24 h period of circadian rhythmicity in Drosophila. Casein Kinase 1 has been shown to be a component of the circadian clock in mammals. Recent studies are also pointing to a role for glycogen synthase kinase 3 in the mammalian clock.