| Literature DB >> 24582500 |
Hye Jin Nam1, Kyungjin Boo1, Dongha Kim1, Dong-Hee Han2, Han Kyoung Choe3, Chang Rok Kim1, Woong Sun4, Hyun Kim4, Kyungjin Kim3, Ho Lee5, Eric Metzger6, Roland Schuele6, Seung-Hee Yoo7, Joseph S Takahashi7, Sehyung Cho2, Gi Hoon Son8, Sung Hee Baek9.
Abstract
The circadian clock is a self-sustaining oscillator that controls daily rhythms. For the proper circadian gene expression, dynamic changes in chromatin structure are important. Although chromatin modifiers have been shown to play a role in circadian gene expression, the in vivo role of circadian signal-modulated chromatin modifiers at an organism level remains to be elucidated. Here, we provide evidence that the lysine-specific demethylase 1 (LSD1) is phosphorylated by protein kinase Cα (PKCα) in a circadian manner and the phosphorylated LSD1 forms a complex with CLOCK:BMAL1 to facilitate E-box-mediated transcriptional activation. Knockin mice bearing phosphorylation-defective Lsd1(SA/SA) alleles exhibited altered circadian rhythms in locomotor behavior with attenuation of rhythmic expression of core clock genes and impaired phase resetting of circadian clock. These data demonstrate that LSD1 is a key component of the molecular circadian oscillator, which plays a pivotal role in rhythmicity and phase resetting of the circadian clock.Entities:
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Year: 2014 PMID: 24582500 DOI: 10.1016/j.molcel.2014.01.028
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970