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10.1111/dom.12514

http://scihub22266oqcxt.onion/10.1111/dom.12514
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C4560116!4560116 !26332962
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suck abstract from ncbi


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pmid26332962
      Diabetes+Obes+Metab 2015 ; 17 Suppl 1 (0 1 ): 6-11
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  • Molecular components of the circadian clock in mammals #MMPMID26332962
  • Takahashi JS
  • Diabetes Obes Metab 2015[Sep]; 17 Suppl 1 (0 1 ): 6-11 PMID26332962 show ga
  • The circadian clock mechanism in animals involves a transcriptional feedback loop in which the bHLH-PAS proteins CLOCK and BMAL1 form a transcriptional activator complex to activate the transcription of the Period and Cryptochrome genes, which in turn feed back to repress their own transcription. In the mouse liver, CLOCK and BMAL1 interact with the regulatory regions of thousands of genes, which are both cyclically and constitutively expressed. The circadian transcription in the liver is clustered in phase and this is accompanied by circadian occupancy of RNA polymerase II recruitment and initiation. These changes also lead to circadian fluctuations in histone H3 lysine4 trimethylation (H3K4me3) as well as H3 lysine9 acetylation (H3K9ac) and H3 lysine27 acetylation (H3K27ac). Thus, the circadian clock regulates global transcriptional poise and chromatin state by regulation of RNA polymerase II.
  • |ARNTL Transcription Factors/*genetics/physiology [MESH]
  • |Acetylation [MESH]
  • |Animals [MESH]
  • |Basic Helix-Loop-Helix Transcription Factors/genetics [MESH]
  • |CLOCK Proteins/*genetics/physiology [MESH]
  • |Circadian Clocks/*genetics [MESH]
  • |Gene Expression [MESH]
  • |Histones/metabolism [MESH]
  • |Humans [MESH]
  • |Liver/physiology [MESH]
  • |Lysine/metabolism [MESH]
  • |Mammals/*genetics [MESH]
  • |Mice [MESH]
  • |Models, Biological [MESH]
  • |RNA Polymerase II/metabolism [MESH]


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