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10.1016/j.bpj.2014.07.022

http://scihub22266oqcxt.onion/10.1016/j.bpj.2014.07.022
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C4167299!4167299!25229153
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suck abstract from ncbi


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pmid25229153      Biophys+J 2014 ; 107 (6): 1462-73
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  • A Mammalian Circadian Clock Model Incorporating Daytime Expression Elements #MMPMID25229153
  • Jolley C; Ukai-Tadenuma M; Perrin D; Ueda H
  • Biophys J 2014[Sep]; 107 (6): 1462-73 PMID25229153show ga
  • Models of the mammalian clock have traditionally been based around two feedback loops?the self-repression of Per/Cry by interfering with activation by BMAL/CLOCK, and the repression of Bmal/Clock by the REV-ERB proteins. Recent experimental evidence suggests that the D-box, a transcription factor binding site associated with daytime expression, plays a larger role in clock function than has previously been understood. We present a simplified clock model that highlights the role of the D-box and illustrate an approach for finding maximum-entropy ensembles of model parameters, given experimentally imposed constraints. Parameter variability can be mitigated using prior probability distributions derived from genome-wide studies of cellular kinetics. Our model reproduces predictions concerning the dual regulation of Cry1 by the D-box and Rev-ErbA/ROR response element (RRE) promoter elements and allows for ensemble-based predictions of phase response curves (PRCs). Nonphotic signals such as Neuropeptide Y (NPY) may act by promoting Cry1 expression, whereas photic signals likely act by stimulating expression from the E/E' box. Ensemble generation with parameter probability restraints reveals more about a model?s behavior than a single optimal parameter set.
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