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      Phosphorylation of LSD1 by PKCα is crucial for circadian rhythmicity and phase resetting.

      Molecular Cell
      ARNTL Transcription Factors, metabolism, Amino Acid Sequence, Animals, Behavior, Animal, CLOCK Proteins, Chromatin Immunoprecipitation, Circadian Rhythm, Gene Expression Regulation, Light, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Molecular Sequence Data, Oscillometry, Oxidoreductases, N-Demethylating, genetics, Phosphorylation, Promoter Regions, Genetic, Protein Kinase C-alpha, Sequence Homology, Amino Acid, Suprachiasmatic Nucleus, Time Factors

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          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. Copyright © 2014 Elsevier Inc. All rights reserved.

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