Cited by 373Circadian rhythm and melatoninSleep and Work-Related FatigueCircular RNAs in diseases

A Role for Glycogen Synthase Kinase-3β in the Mammalian Circadian Clock

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Iitaka, Chisato, Miyazaki, Koyomi, Akaike, Toshihiro, Ishida, Norio·2005·Journal of Biological Chemistry

Abstract

The Drosophila shaggy gene product is a mammalian glycogen synthase kinase-3beta (GSK-3beta) homologue that contributes to the circadian clock of the Drosophila through TIMELESS phosphorylation, and it regulates nuclear translocation of the PERIOD/TIMELESS heterodimer. We found that mammalian GSK-3beta is expressed in the suprachiasmatic nucleus and liver of mice and that GSK-3beta phosphorylation exhibits robust circadian oscillation. Rhythmic GSK-3beta phosphorylation is also observed in serum-shocked NIH3T3 cells. Exposing serum-shocked NIH3T3 cells to lithium chloride, a specific inhibitor of GSK-3beta, increases GSK-3beta phosphorylation and delays the phase of rhythmic clock gene expression. On the other hand, GSK-3beta overexpression advances the phase of clock gene expression. We also found that GSK-3beta interacts with PERIOD2 (PER2) in vitro and in vivo. Recombinant GSK-3beta can phosphorylate PER2 in vitro. GSK-3beta promotes the nuclear translocation of PER2 in COS1 cells. The present data suggest that GSK-3beta plays important roles in mammalian circadian clock.

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Crossref · 10.1074/jbc.m503526200

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  • PER and CRY proteins are phosphorylated by Casein Kinase I ε and δ and Glycogen Synthase Kinase 3β, leading to changes in their stability, association, and nuclear entry.

    “The PER and CRY proteins are translated in the cytoplasm, and are phosphorylated by Casein Kinase I ε and δ (CK1) and Glycogen Synthase Kinase 3β (GSK3β), leading to changes in their stability, association, and nuclear entry (Harms et al., 2003; Iitaka et al., 2005; Knippschild et al., 2005; Kurabayashi et al., 2006).”

    From Circadian genes, rhythms and the biology of mood disorders (2007) · cites this paper as Iitaka et al., 2005

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References 44 · Cited by 373

Authors
Iitaka, C., Miyazaki, K., Akaike, T., & Ishida, N.
Affiliations
  • Tokyo Institute of Technology (JP)
  • National Institute of Advanced Industrial Science and Technology (JP)
  • University of Tsukuba (JP)
Corresponding author
Ishida, Norio
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2005-08
Volume
280
Issue
33
Pages
29397-29402
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2078086032
Cited by
373
References
44
Citations by year
2026: 11 · 2025: 7 · 2024: 9 · 2023: 8 · 2022: 14 · 2021: 24 · 2020: 19 · 2019: 9 · 2018: 16 · 2017: 17 · 2016: 16 · 2015: 21 · 2014: 16 · 2013: 21 · 2012: 26
FWCI
7.24
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Circular RNAs in diseases
Keywords
glycogen synthase kinase-3β, circadian clock, Per2, Period2, Shaggy, TIMELESS, suprachiasmatic nucleus, liver, clock gene expression, lithium chloride, nuclear translocation, protein phosphorylation, serum shock, NIH3T3 cells
MeSH terms
Glycogen Synthase Kinase 3 beta, Animals, Binding Sites, Circadian Rhythm, Mice, Inbred ICR, Nuclear Proteins, Phosphorylation, RNA, Messenger, Transcription Factors, Cell Cycle Proteins, Active Transport, Cell Nucleus, Glycogen Synthase Kinase 3, NIH 3T3 Cells, Mice, Basic Helix-Loop-Helix Transcription Factors, Basic Helix-Loop-Helix Proteins, ARNTL Transcription Factors, Period Circadian Proteins

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