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ASK family kinases mediate cellular stress and redox signaling to circadian clock.

Authors :
Kiyomichi Imamura
Hikari Yoshitane
Kazuki Hattori
Mitsuo Yamaguchi
Kento Yoshida
Takenori Okubo
Isao Naguro
Hidenori Ichijo
Yoshitaka Fukada
Source :
Proceedings of the National Academy of Sciences of the United States of America; 4/3/2018, Vol. 115 Issue 14, p3646-3651, 6p
Publication Year :
2018

Abstract

Daily rhythms of behaviors and physiologies are generated by the circadian clock, which is composed of clock genes and the encoded proteins forming transcriptional/translational feedback loops (TTFLs). The circadian clock is a self-sustained oscillator and flexibly responds to various time cues to synchronize with environmental 24-h cycles. However, the key molecule that transmits cellular stress to the circadian clockwork is unknown. Here we identified apoptosis signal-regulating kinase (ASK), a member of the MAPKKK family, as an essential mediator determining the circadian period and phase of cultured cells in response to osmotic changes of the medium. The physiological impact of ASK signaling was demonstrated by a response of the clock to changes in intracellular redox states. Intriguingly, the TTFLs drive rhythmic expression of Ask genes, indicating ASK-mediated association of the TTFLs with intracellular redox. In behavioral analysis, Ask1, Ask2, and Ask3 triple-KO mice exhibited compromised light responses of the circadian period and phase in their activity rhythms. LC-MS/MS-based proteomic analysis identified a series of ASK-dependent and osmotic stress-responsive phosphorylations of proteins, among which CLOCK, a key component of the molecular clockwork, was phosphorylated at Thr843 or Ser845 in the carboxyl-terminal region. These findings reveal the ASK-dependent stress response as an underlying mechanism of circadian clock flexibility. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
115
Issue :
14
Database :
Complementary Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
128909467
Full Text :
https://doi.org/10.1073/pnas.1719298115