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Cyclin-dependent kinase 5 (Cdk5) regulates the function of CLOCK protein by direct phosphorylation.

Authors :
Kwak Y
Jeong J
Lee S
Park YU
Lee SA
Han DH
Kim JH
Ohshima T
Mikoshiba K
Suh YH
Cho S
Park SK
Source :
The Journal of biological chemistry [J Biol Chem] 2013 Dec 27; Vol. 288 (52), pp. 36878-89. Date of Electronic Publication: 2013 Nov 14.
Publication Year :
2013

Abstract

Circadian rhythm is a biological rhythm governing physiology and behavior with a period of ∼24 h. At the molecular level, circadian output is controlled by a molecular clock composed of positive and negative feedback loops in transcriptional and post-translational processes. CLOCK is a transcription factor known as a central component of the molecular clock feedback loops generating circadian oscillation. Although CLOCK is known to undergo multiple post-translational modifications, the knowledge of their entities remains limited. Cyclin-dependent kinase 5 (Cdk5) is a proline-directed serine-threonine kinase that is involved in various neuronal processes. Here, we report that Cdk5 is a novel regulator of CLOCK protein. Cdk5 phosphorylates CLOCK at the Thr-451 and Thr-461 residues in association with transcriptional activation of CLOCK. The Cdk5-dependent regulation of CLOCK function is mediated by alterations of its stability and subcellular distribution. These results suggest that Cdk5 is a novel regulatory component of the core molecular clock machinery.

Details

Language :
English
ISSN :
1083-351X
Volume :
288
Issue :
52
Database :
MEDLINE
Journal :
The Journal of biological chemistry
Publication Type :
Academic Journal
Accession number :
24235147
Full Text :
https://doi.org/10.1074/jbc.M113.494856