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Translation regulation in sleep

Seibt, Julie and Frank, Marcos G (2012) Translation regulation in sleep Communicative & Integrative Biology, 5 (5). pp. 491-495.

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Abstract

Sleep improves cognition and is necessary for normal brain plasticity, but the precise cellular and molecular mechanisms mediating these effects are unknown. At the molecular level, experience-dependent synaptic plasticity triggers new gene and protein expression necessary for long-lasting changes in synaptic strength.1 In particular, translation of mRNAs at remodeling synapses is emerging as an important mechanism in persistent forms of synaptic plasticity in vitro and certain forms of memory consolidation.2 We have previously shown that sleep is required for the consolidation of a canonical model of in vivo plasticity (i.e., ocular dominance plasticity [ODP] in the developing cat).3 Using this model, we recently showed that protein synthesis during sleep participates in the consolidation process. We demonstrate that activation of the mammalian target of rapamycin [mTOR] pathway, an important regulator of translation initiation,4 is necessary for sleep-dependent ODP consolidation and that sleep promotes translation (but not transcription) of proteins essential for synaptic plasticity (i.e., ARC and BDNF). Our study thus reveals a previously unknown mechanism operating during sleep that consolidates cortical plasticity in vivo.

Item Type: Article
Divisions : Faculty of Health and Medical Sciences > School of Biosciences and Medicine
Authors :
NameEmailORCID
Seibt, Juliej.seibt@surrey.ac.uk
Frank, Marcos G
Date : 1 September 2012
DOI : 10.4161/cib.21010
Copyright Disclaimer : Copyright © 2012 Landes Bioscience
Uncontrolled Keywords : development, mRNA, ontogeny, plasticity, protein synthesis, translation
Depositing User : Melanie Hughes
Date Deposited : 28 Aug 2018 12:57
Last Modified : 28 Aug 2018 12:57
URI: http://epubs.surrey.ac.uk/id/eprint/849126

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