Multiple random phosphorylations in clock proteins provide long delays and switches
説明
<jats:title>Abstract</jats:title><jats:p>Theory predicts that self-sustained oscillations require robust delays and nonlinearities (ultrasensitivity). Delayed negative feedback loops with switch-like inhibition of transcription constitute the core of eukaryotic circadian clocks. The kinetics of core clock proteins such as PER2 in mammals and FRQ in <jats:italic>Neurospora crassa</jats:italic> is governed by multiple phosphorylations. We investigate how multiple, slow and random phosphorylations control delay and molecular switches. We model phosphorylations of intrinsically disordered clock proteins (IDPs) using conceptual models of sequential and distributive phosphorylations. Our models help to understand the underlying mechanisms leading to delays and ultrasensitivity. The model shows temporal and steady state switches for the free kinase and the phosphoprotein. We show that random phosphorylations and sequestration mechanisms allow high Hill coefficients required for self-sustained oscillations.</jats:p>
収録刊行物
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- Scientific Reports
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Scientific Reports 10 (1), 2020-12-17
Springer Science and Business Media LLC