A role for cryptochromes in sleep regulation Public Deposited

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Creator
  • Kilduff, Thomas S
    • Other Affiliation: Molecular Neurobiology Laboratory, SRI International, Menlo Park, CA, USA
  • O'Hara, Bruce F
    • Other Affiliation: Dept. of Biological Sciences, Stanford University, Stanford, CA, USA
  • Sancar, Aziz
    • Affiliation: School of Medicine, Department of Biochemistry and Biophysics
  • Franken, Paul
    • Other Affiliation: Dept. of Biological Sciences, Stanford University, Stanford, CA, USA
  • Edgar, Dale M
    • Other Affiliation: Dept. of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA
  • Selby, Chris P
    • Affiliation: School of Medicine, Department of Biochemistry and Biophysics
  • Terao, Akira
    • Other Affiliation: Molecular Neurobiology Laboratory, SRI International, Menlo Park, CA, USA
  • Wisor, Jonathan P
    • Other Affiliation: Dept. of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA
Abstract
  • Abstract: Background: The cryptochrome 1 and 2 genes (cry1 and cry2) are necessary for the generation of circadian rhythms, as mice lacking both of these genes (cry1,2-/-) lack circadian rhythms. We studied sleep in cry1,2-/- mice under baseline conditions as well as under conditions of constant darkness and enforced wakefulness to determine whether cryptochromes influence sleep regulatory processes. Results: Under all three conditions, cry1,2-/- mice exhibit the hallmarks of high non-REM sleep (NREMS) drive (i.e., increases in NREMS time, NREMS consolidation, and EEG delta power during NREMS). This unexpected phenotype was associated with elevated brain mRNA levels of period 1 and 2 (per1,2), and albumin d-binding protein (dbp), which are known to be transcriptionally inhibited by CRY1,2. To further examine the relationship between circadian genes and sleep homeostasis, we examined wild type mice and rats following sleep deprivation and found increased levels of per1,2 mRNA and decreased levels of dbp mRNA specifically in the cerebral cortex; these changes subsided with recovery sleep. The expression of per3, cry1,2, clock, npas2, bmal1, and casein-kinase- 1ε did not change with sleep deprivation. Conclusions: These results indicate that mice lacking cryptochromes are not simply a genetic model of circadian arrhythmicity in rodents and functionally implicate cryptochromes in the homeostatic regulation of sleep.
Date of publication
Identifier
  • doi:10.1186/1471-2202-3-20
  • 12495442
Resource type
  • Article
Rights statement
  • In Copyright
Rights holder
  • Jonathan P Wisor et al.; licensee BioMed Central Ltd.
Journal title
  • BMC Neuroscience
Journal volume
  • 3
Journal issue
  • 1
Page start
  • 20
Language
  • English
Is the article or chapter peer-reviewed?
  • Yes
ISSN
  • 1471-2202
Bibliographic citation
  • BMC Neuroscience. 2002 Dec 20;3(1):20
Access
  • Open Access
Publisher
  • BioMed Central Ltd
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