A Role for Casein Kinase 2 in the Mechanism Underlying Circadian Temperature Compensation

• Published in: Cell Vol. 137; no. 4; pp. 749 - 760
• Main Authors: Mehra, Arun, Shi, Mi, Baker, Christopher L., Colot, Hildur V., Loros, Jennifer J., Dunlap, Jay C.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.05.2009
• Subjects: Casein Kinase II - chemistry; Casein Kinase II - genetics; Casein Kinase II - physiology; CELLBIO; Circadian Rhythm; Gene Dosage; Mutation; Neurospora crassa - enzymology; Neurospora crassa - physiology; Phosphoric Monoester Hydrolases - metabolism; Phosphotransferases - metabolism; Protein Subunits - chemistry; Protein Subunits - genetics; Protein Subunits - physiology; PROTEINS; SYSBIO; Temperature; CELLBIO; SYSBIO; PROTEINS
• ISSN: 0092-8674; 1097-4172
• DOI: 10.1016/j.cell.2009.03.019

Temperature compensation of circadian clocks is an unsolved problem with relevance to the general phenomenon of biological compensation. We identify casein kinase 2 (CK2) as a key regulator of temperature compensation of the Neurospora clock by determining that two long-standing clock mutants, chrono and period-3, displaying distinctive alterations in compensation encode the β1 and α subunits of CK2, respectively. Reducing the dose of these subunits, particularly β1, significantly alters temperature compensation without altering the enzyme's Q 10. By contrast, other kinases and phosphatases implicated in clock function do not play appreciable roles in temperature compensation. CK2 exerts its effects on the clock by directly phosphorylating FREQUENCY (FRQ), and this phosphorylation is compromised in CK2 hypomorphs. Finally, mutation of certain putative CK2 phosphosites on FRQ, shown to be phosphorylated in vivo, predictably alters temperature compensation profiles effectively phenocopying CK2 mutants.