The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses (Q28208647)

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Marcello Giorgi

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Beatrice Primerano

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Annamaria Moro

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Alessandra Di Penta

5

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Surya Reis

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Claudia Bagni

Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

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language of work or name

English

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publication date

7 February 2003

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published in

Cell

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volume

112

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issue

3

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page(s)

317-27

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cites work

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7 January 2021

FMR1 protein: conserved RNP family domains and selective RNA binding

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Chemical stimulation of synaptosomes modulates alpha -Ca2+/calmodulin-dependent protein kinase II mRNA association to polysomes.

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Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes.

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A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

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On "genomenclature": a comprehensive (and respectful) taxonomy for pseudogenes and other "junk DNA"

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Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein

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Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

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Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

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7 January 2021

Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle

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7 January 2021

Identification and characterization of BC1 RNP particles

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7 January 2021

Expression of dendritic BC200 RNA, component of a 11.4S ribonucleoprotein particle, is conserved in humans and simians.

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7 January 2021

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

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The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes

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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

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A point mutation in the FMR-1 gene associated with fragile X mental retardation

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7 January 2021

The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals

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7 January 2021

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes

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Selective localization of messenger RNA for cytoskeletal protein MAP2 in dendrites

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Fragile X syndrome without CCG amplification has an FMR1 deletion

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Synaptic regulation of protein synthesis and the fragile X protein

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Analysis of neocortex in three males with the fragile X syndrome

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The fragile X mental retardation protein is associated with ribosomes

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7 January 2021

Evidence that fragile X mental retardation protein is a negative regulator of translation

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7 January 2021

The fragile X mental retardation protein inhibits translation via interacting with mRNA

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7 January 2021

Somatodendritic expression of an immediate early gene is regulated by synaptic activity

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7 January 2021

Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites

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7 January 2021

Local protein synthesis and its role in synapse-specific plasticity

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7 January 2021

BC200 RNA: a neural RNA polymerase III product encoded by a monomeric Alu element

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7 January 2021

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression

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7 January 2021

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

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Rare variants in the promoter of the fragile X syndrome gene (FMR1)

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7 January 2021

LTP, memory and structural plasticity

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7 January 2021

RNA transport in dendrites: a cis-acting targeting element is contained within neuronal BC1 RNA

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7 January 2021

Abnormal development of dendritic spines in FMR1 knock-out mice

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7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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7 January 2021

A decade of molecular studies of fragile X syndrome

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7 January 2021

Functions of the fragile X protein

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7 January 2021

From factors to mechanisms: translation and translational control in eukaryotes.

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7 January 2021

Selective translation of mRNAs at synapses

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7 January 2021

Neuronal BC1 RNA structure: evolutionary conversion of a tRNA(Ala) domain into an extended stem-loop structure

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7 January 2021

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

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7 January 2021

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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7 January 2021

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

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7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

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7 January 2021

CaM-kinases: modulators of synaptic plasticity

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7 January 2021

Protein synthesis at synaptic sites on dendrites

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7 January 2021

RNAs that interact with the fragile X syndrome RNA binding protein FMRP.

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7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

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7 January 2021

FMRP is associated to the ribosomes via RNA.

1 reference

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7 January 2021

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

1 reference

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7 January 2021

Dendritic location of neural BC1 RNA

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900079-5

7 January 2021

Primary structure, neural-specific expression, and dendritic location of human BC200 RNA.

1 reference

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7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900079-5

7 January 2021

Dendritic BC1 RNA: functional role in regulation of translation initiation.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900079-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900079-5

7 January 2021

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

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7 January 2021

Computer prediction of RNA structure

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7 January 2021

10.1016/S0092-8674(03)00079-5

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

2216886

2216886

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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