Professor Hiroki Ueda, Assistant Professor Daisuke Tone, Lecturer Koji Ode, and Qianhui Zhang (4th-year graduate student at the time) at the University of Tokyo showed that CaMKIIβ(1)a predominant protein kinase expressed in neurons, is involved in prolonging the sleep duration via facilitating sleep onset and inhibiting awakening.
Several recent studies have shown that protein phosphorylation(2) is important for sleep regulation. The aforementioned study group reported in 2016 that CaMKIIα and CaMKIIβ are protein kinases that promote sleep and suggested the possibility that protein phosphorylation is the likely molecular driver of somnolence and proposed “phosphorylation hypothesis of sleep”. CaMKIIα and CaMKIIβ are abundantly expressed in brain nerve cells and have been extensively studied to show their important role in functions such as memory. However, the functions and conditions of CaMKIIα and CaMKIIβ in sleep control were unknown.
It is well-known that CaMKIIβ has multiple phosphorylation sites and that its function is modulated according to their phosphorylation status(3). Therefore, this study group generated a series of CaMKIIβ mutants. Toward this, mutated residues that mimic the phosphorylation state were introduced at each site, and the relationship between CaMKIIβ phosphorylation state and sleep regulation was comprehensively investigated using mice. The researchers found that in specific phosphorylation state, CaMKIIβ promoted the transition from wakefulness to sleep state. Furthermore, when an additional second or third similarly phosphorylated variant was introduced into CaMKIIβ in this specific phosphorylated state, transition from the sleep state to wakefulness was inhibited.
In the present study, they found that CaMKIIβ functions at each step of a multi-step process that prolongs sleep duration (induction and maintenance of sleep) depending on its state of phosphorylation. Many existing hypnotics act on the steps involved in the induction of sleep. This study partly clarified the mechanism underlying sleep induction and maintenance and provides clues to consider more ideal sleep control methods aimed at maintaining sleep, which has been difficult so far.
This result was obtained as part of the JST Exploratory Research for Advanced Technology (ERATO) under the “Ueda Biological Timing Project”. In this project, JST developed an approach based on “systems biology contributing to human understanding” using sleep–wake rhythms as a model. The aim was to obtain information related to “biological timing” that extends from molecules to individuals, in terms of human sleep–wake cycle.
Ca2+Calmodulin-dependent protein kinase II. It is abundant in nerve cells and is activated by Ca2+/calmodulin binding. The α, β, δ, and γ subtypes are known, and these subunits form 12-mers. In addition to phosphorylating other proteins as kinases, they also regulate the activity of nerve cells by forming complexes with a variety of proteins. Phosphorylation is known to occur, especially on serine, threonine, and tyrosine residues, among the 20 amino acids that comprise proteins. Of these, CaMKII undergoes phosphorylation at serine and threonine.
In vivo, proteins are produced following the transcription and translation of genes, and can undergo chemical modification, which regulates their function. Among these, phosphorylation is a post-translational modification that occurs in most proteins.
Kinases phosphorylate other proteins, but they might also phosphorylate and modify themselves. This is called autophosphorylation. It is a convenient mechanism for feedback control because the function of the kinase itself can be controlled via the action of the kinase. There are several well-known sites in CaMKIIβ modified by autophosphorylation.
Method of Research
Subject of Research
Distinct phosphorylation states of mammalian CaMKIIβ control the induction and maintenance of sleep
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