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Augmented generation of protein fragments during wakefulness as the molecular cause of sleep: A hypothesis

Varshavsky, Alexander (2012) Augmented generation of protein fragments during wakefulness as the molecular cause of sleep: A hypothesis. Protein Science, 21 (11). ISSN 0961-8368. PMCID PMC3527701. doi:10.1002/pro.2148. https://resolver.caltech.edu/CaltechAUTHORS:20120831-090649691

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Abstract

Despite extensive understanding of sleep regulation, the molecular-level cause and function of sleep are unknown. I suggest that they originate in individual neurons and stem from increased production of protein fragments during wakefulness. These fragments are transient parts of protein complexes in which the fragments were generated. Neuronal Ca^(2+) fluxes are higher during wakefulness than during sleep. Subunits of transmembrane channels and other proteins are cleaved by Ca^(2+)-activated calpains and by other nonprocessive proteases, including caspases and secretases. In the proposed concept, termed the fragment generation (FG) hypothesis, sleep is a state during which the production of fragments is decreased (owing to lower Ca^(2+) transients) while fragment-destroying pathways are upregulated. These changes facilitate the elimination of fragments and the remodeling of protein complexes in which the fragments resided. The FG hypothesis posits that a proteolytic cleavage, which produces two fragments, can have both deleterious effects and fitness-increasing functions. This (previously not considered) dichotomy can explain both the conservation of cleavage sites in proteins and the evolutionary persistence of sleep, because sleep would counteract deleterious aspects of protein fragments. The FG hypothesis leads to new explanations of sleep phenomena, including a longer sleep after sleep deprivation. Studies in the 1970s showed that ethanol-induced sleep in mice can be strikingly prolonged by intracerebroventricular injections of either Ca^(2+) alone or Ca^(2+) and its ionophore. These results, which were never interpreted in connection to protein fragments or the function of sleep, may be accounted for by the FG hypothesis about molecular causation of sleep.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1002/pro.2148DOIArticle
http://onlinelibrary.wiley.com/doi/10.1002/pro.2148/abstractPublisherArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527701/PubMed CentralArticle
ORCID:
AuthorORCID
Varshavsky, Alexander0000-0002-4011-258X
Additional Information:© 2012 The Protein Society. Received 2 August 2012; Accepted 21 August 2012. Published online 28 August 2012. I thank Christopher Brower, Raymond Deshaies, William Dunphy, Konstantin Piatkov, Jevgenij Raskatov, Connor Rosen, Brenda Schulman, Anna Shemorry, and Brandon Wadas for helpful discussions and comments on the manuscript. I am particularly grateful to Roger Kornberg and William Tansey for their detailed suggestions. Our studies of the ubiquitin system and the N-end rule pathway are supported by grants from the National Institutes of Health.
Funders:
Funding AgencyGrant Number
NIHDK039520
NIHGM031530
Subject Keywords:neurons; proteolysis; N-end rule; remodeling; memory; muscle
Issue or Number:11
PubMed Central ID:PMC3527701
DOI:10.1002/pro.2148
Record Number:CaltechAUTHORS:20120831-090649691
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20120831-090649691
Official Citation:Varshavsky, A. (2012), Augmented generation of protein fragments during wakefulness as the molecular cause of sleep: a hypothesis. Protein Science, 21: 1634–1661. doi:10.1002/pro.2148
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:33753
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:31 Aug 2012 16:40
Last Modified:09 Nov 2021 21:37

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