CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.

Détails

ID Serval
serval:BIB_D5BA669148FB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.
Périodique
Neuron
Auteur(s)
De Rubeis S., Pasciuto E., Li K.W., Fernández E., Di Marino D., Buzzi A., Ostroff L.E., Klann E., Zwartkruis F.J., Komiyama N.H., Grant S.G., Poujol C., Choquet D., Achsel T., Posthuma D., Smit A.B., Bagni C.
ISSN
1097-4199 (Electronic)
ISSN-L
0896-6273
Statut éditorial
Publié
Date de publication
18/09/2013
Volume
79
Numéro
6
Pages
1169-1182
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
The CYFIP1/SRA1 gene is located in a chromosomal region linked to various neurological disorders, including intellectual disability, autism, and schizophrenia. CYFIP1 plays a dual role in two apparently unrelated processes, inhibiting local protein synthesis and favoring actin remodeling. Here, we show that brain-derived neurotrophic factor (BDNF)-driven synaptic signaling releases CYFIP1 from the translational inhibitory complex, triggering translation of target mRNAs and shifting CYFIP1 into the WAVE regulatory complex. Active Rac1 alters the CYFIP1 conformation, as demonstrated by intramolecular FRET, and is key in changing the equilibrium of the two complexes. CYFIP1 thus orchestrates the two molecular cascades, protein translation and actin polymerization, each of which is necessary for correct spine morphology in neurons. The CYFIP1 interactome reveals many interactors associated with brain disorders, opening new perspectives to define regulatory pathways shared by neurological disabilities characterized by spine dysmorphogenesis.

Mots-clé
Adaptor Proteins, Signal Transducing/chemistry, Adaptor Proteins, Signal Transducing/genetics, Adaptor Proteins, Signal Transducing/metabolism, Age Factors, Aminoquinolines/pharmacology, Analysis of Variance, Animals, Brain-Derived Neurotrophic Factor/pharmacology, Carbazoles/pharmacology, Cells, Cultured, Cerebral Cortex/cytology, Chromatography, Liquid, DNA-Binding Proteins/metabolism, Dendritic Spines/drug effects, Dendritic Spines/genetics, Dendritic Spines/ultrastructure, Enzyme Inhibitors/pharmacology, Fragile X Mental Retardation Protein/genetics, Fragile X Mental Retardation Protein/metabolism, Fragile X Mental Retardation Protein/ultrastructure, Gene Expression Regulation/genetics, Green Fluorescent Proteins/genetics, Green Fluorescent Proteins/metabolism, Humans, Immunoprecipitation, In Vitro Techniques, Indole Alkaloids/pharmacology, Luminescent Proteins/metabolism, Male, Mental Disorders/genetics, Meta-Analysis as Topic, Mice, Mice, Inbred C57BL, Mice, Transgenic, Microscopy, Immunoelectron, Nerve Tissue Proteins/chemistry, Nerve Tissue Proteins/genetics, Nerve Tissue Proteins/metabolism, Nerve Tissue Proteins/ultrastructure, Neurons/drug effects, Neurons/ultrastructure, Protein Biosynthesis/drug effects, Protein Biosynthesis/genetics, Pyrimidines/pharmacology, RNA, Messenger/metabolism, Synaptosomes/drug effects, Synaptosomes/metabolism, Synaptosomes/ultrastructure, Tandem Mass Spectrometry, Time Factors, Transcription Factors/metabolism, Transfection
Pubmed
Open Access
Oui
Création de la notice
06/03/2017 17:23
Dernière modification de la notice
20/08/2019 15:55
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