The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP (Q24314573)

Cytoplasmic FMR1 interacting protein 1

GOA release 2020-03-11

1 reference

Eukaryotic translation initiation factor 4E

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

13

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Pietro Pilo Boyl

Pietro Pilo Boyl

3

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Silvia De Rubeis

Silvia De Rubeis

6

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Francesca Zalfa

Francesca Zalfa

5

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Claudia Bagni

Claudia Bagni

15

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Mattia Falconi

Mattia Falconi

10

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Valentina Mercaldo

2

Valentina Mercaldo

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author name string

Ilaria Napoli

1

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Boris Eleuteri

4

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Daniele Di Marino

7

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Evita Mohr

8

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Marzia Massimi

9

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Walter Witke

11

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Mauro Costa-Mattioli

12

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Tilmann Achsel

Repression of cap-dependent translation by 4E-binding protein 1: competition with p220 for binding to eukaryotic initiation factor-4E

14

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language of work or name

English

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publication date

19 September 2008

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published in

Cell

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volume

134

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page(s)

1042-54

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issue

6

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cites work

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Structural basis for mRNA Cap-Binding regulation of eukaryotic initiation factor 4E by 4E-binding protein, studied by spectroscopic, X-ray crystal structural, and molecular dynamics simulation methods

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Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome.

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Function and regulation of local axonal translation

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Abi, Sra1, and Kette control the stability and localization of SCAR/WAVE to regulate the formation of actin-based protrusions

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Regulation of dendritic spine motility and stability by Rac1 and Rho kinase: evidence for two forms of spine motility

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The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines

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Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression

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Correction of fragile X syndrome in mice.

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Shared protein components of SINE RNPs

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Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function.

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The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

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Dynamic visualization of local protein synthesis in hippocampal neurons

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RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

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CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

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Compartmentalized synthesis and degradation of proteins in neurons.

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Local protein synthesis and its role in synapse-specific plasticity

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Translational control by the 3'-UTR: the ends specify the means.

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Cap-dependent translation initiation in eukaryotes is regulated by a molecular mimic of eIF4G

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Regulation of cap-dependent translation by eIF4E inhibitory proteins

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A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability

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Molecular mechanisms of translational control

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From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

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Drosophila Cup is an eIF4E-binding protein that functions in Smaug-mediated translational repression

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Profilin2 contributes to synaptic vesicle exocytosis, neuronal excitability, and novelty-seeking behavior

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The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development.

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The brain-derived neurotrophic factor enhances synthesis of Arc in synaptoneurosomes

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Fragile X mental retardation protein FMRP and the RNA export factor NXF2 associate with and destabilize Nxf1 mRNA in neuronal cells

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Altered synaptic plasticity in a mouse model of fragile X mental retardation

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A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

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Metabotropic glutamate receptors trigger postsynaptic protein synthesis

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Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

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Proteolysis of human eukaryotic translation initiation factor eIF4GII, but not eIF4GI, coincides with the shutoff of host protein synthesis after poliovirus infection

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Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

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The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

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Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

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The fragile X mental retardation protein has nucleic acid chaperone properties

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The Prader-Willi phenotype of fragile X syndrome

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Translational control by neuroguidin, a eukaryotic initiation factor 4E and CPEB binding protein

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The translation initiation factor eIF-4E binds to a common motif shared by the translation factor eIF-4 gamma and the translational repressors 4E-binding proteins

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Sra-1 interacts with Kette and Wasp and is required for neuronal and bristle development in Drosophila.

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FMRP mediates mGluR5-dependent translation of amyloid precursor protein

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Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses

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The brain cytoplasmic RNA BC1 regulates dopamine D2 receptor-mediated transmission in the striatum

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FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A.

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