| Literature DB >> 22441692 |
Hikari Yoshitane1, Sato Honma, Kiyomichi Imamura, Hiroto Nakajima, Shin-ya Nishide, Daisuke Ono, Hiroshi Kiyota, Naoya Shinozaki, Hirokazu Matsuki, Naoya Wada, Hirofumi Doi, Toshiyuki Hamada, Ken-ichi Honma, Yoshitaka Fukada.
Abstract
The posttranslational regulation of mammalian clock proteins has been assigned a time-keeping function, but seems to have more essential roles. Here we show that c-Jun N-terminal kinase (JNK), identified by inhibitor screening of BMAL1 phosphorylation at Ser 520/Thr 527/Ser 592, confers dynamic regulation on the clock. Knockdown of JNK1 and JNK2 abrogates BMAL1 phosphorylation and lengthens circadian period in fibroblasts. Mice deficient for neuron-specific isoform JNK3 have altered behavioural rhythms, with longer free-running period and compromised phase shifts to light. The locomotor rhythms are insensitive to intensity variance of constant light, deviating from Aschoff's rule. Thus, JNK regulates a core characteristic of the circadian clock by controlling the oscillation speed and the phase in response to light.Entities:
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Year: 2012 PMID: 22441692 PMCID: PMC3343351 DOI: 10.1038/embor.2012.37
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807