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A role for O-GlcNAcylation in setting circadian clock speed

Authors
Kim, EY; Jeong, EH; Park, S; Jeong, HJ; Edery, I; Cho, JW
Citation
Genes & development, 26(5):490-502, 2012
Journal Title
Genes & development
ISSN
0890-93691549-5477
Abstract
Post-translational modifications of one or more central "clock" proteins, most notably time-of-day-dependent changes in phosphorylation, are critical for setting the pace of circadian (≅24 h) clocks. In animals, PERIOD (PER) proteins are the key state variable regulating circadian clock speed and undergo daily changes in abundance and cytoplasmic-nuclear distribution that are partly driven by a complex phosphorylation program. Here, we identify O-GlcNAcylation (O-GlcNAc) as a critical post-translational modification in circadian regulation that also contributes to setting clock speed. Knockdown or overexpression of Drosophila O-GlcNAc transferase (ogt) in clock cells either shortens or lengthens circadian behavioral rhythms, respectively. The Drosophila PERIOD protein (dPER) is a direct target of OGT and undergoes daily changes in O-GlcNAcylation, a modification that is mainly observed during the first half of the night, when dPER is predominantly located in the cytoplasm. Intriguingly, the timing of when dPER translocates from the cytoplasm to the nucleus is advanced or delayed in flies, wherein ogt expression is reduced or increased, respectively. Our results suggest that O-GlcNAcylation of dPER contributes to setting the correct pace of the clock by delaying the timing of dPER nuclear entry. In addition, OGT stabilizes dPER, suggesting that O-GlcNAcylation has multiple roles in circadian timing systems.
MeSH terms
AcylationAnimalsCasein Kinase Iepsilon/metabolismCell LineCell Nucleus/metabolismCells, CulturedCircadian Clocks/*physiologyDrosophila Proteins/metabolismDrosophila melanogaster/metabolism/*physiologyGene Expression Regulation, EnzymologicGene Knockdown TechniquesN-Acetylglucosaminyltransferases/metabolismNeurons/enzymology/metabolismPeriod Circadian Proteins/metabolismRNA, Messenger/metabolism
DOI
10.1101/gad.182378.111
PMID
22327476
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Brain Science
AJOU Authors
김, 은영
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