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Forgetting is regulated via Musashi-mediated translational control of the Arp2/3 complex
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2714682
Author(s) Hadziselimovic, Nils; Vukojevic, Vanja; Peter, Fabian; Milnik, Annette; Fastenrath, Matthias; Fenyves, Bank Gabor; Hieber, Petra; Demougin, Philippe; Vogler, Christian; de Quervain, Dominique J.-F.; Papassotiropoulos, Andreas; Stetak, Attila
Author(s) at UniBasel de Quervain, Dominique
Vukojevic, Vanja
Milnik, Annette
Fastenrath, Matthias
Papassotiropoulos, Andreas
Vogler, Christian
Stetak, Attila
Year 2014
Title Forgetting is regulated via Musashi-mediated translational control of the Arp2/3 complex
Journal Cell
Volume 156
Number 6
Pages / Article-Number 1153-1166
Mesh terms Actin-Related Protein 2-3 Complex, metabolism; Actins, metabolism; Amino Acid Sequence; Animals; Caenorhabditis elegans, metabolism; Caenorhabditis elegans Proteins, metabolism; Interneurons, metabolism; Memory; Molecular Sequence Data; Mutation; Nerve Tissue Proteins, metabolism; Protein Biosynthesis; RNA, Helminth, metabolism; RNA, Messenger, metabolism; RNA-Binding Proteins, metabolism; Sequence Alignment; Synapses
Abstract A plastic nervous system requires the ability not only to acquire and store but also to forget. Here, we report that musashi (msi-1) is necessary for time- dependent memory loss in C. elegans. Tissue- specific rescue demonstrates that MSI-1 function is necessary in the AVA interneuron. Using RNA-bind- ing protein immunoprecipitation (IP), we found that MSI-1 binds to mRNAs of three subunits of the Arp2/3 actin branching regulator complex in vivo and downregulates ARX-1, ARX-2, and ARX-3 trans- lation upon associative learning. The role of msi-1 in forgetting is also reflected by the persistence of learning-induced GLR-1 synaptic size increase in msi-1 mutants. We demonstrate that memory length is regulated cooperatively through the activation of adducin (add-1) and by the inhibitory effect of msi-1. Thus, a GLR-1/MSI-1/Arp2/3 pathway induces forgetting and represents a novel mechanism of memory decay by linking translational control to the structure of the actin cytoskeleton in neurons.
Publisher Cell Press
ISSN/ISBN 0092-8674
edoc-URL http://edoc.unibas.ch/dok/A6243377
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.cell.2014.01.054
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/24630719
ISI-Number WOS:000332945100007
Document type (ISI) Article
 
   

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