A novel function for the survival motoneuron protein as a translational regulator (Q58379271)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23136128%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

title

A novel function for the survival motoneuron protein as a translational regulator (English)

1 reference

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17 February 2020

6

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17 February 2020

Rashmi Kothary

7

1 reference

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17 February 2020

Jocelyn Côté

10

1 reference

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17 February 2020

author name string

Gabriel Sanchez

1

1 reference

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17 February 2020

Olivier Biondi

4

1 reference

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17 February 2020

Helina Tadesse

5

1 reference

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17 February 2020

Frédéric Charbonnier

8

1 reference

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17 February 2020

Alain Y Dury

2

1 reference

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17 February 2020

Lyndsay M Murray

3

1 reference

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17 February 2020

Edouard W Khandjian

9

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17 February 2020

publication date

6 November 2012

1 reference

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17 February 2020

published in

Human Molecular Genetics

1 reference

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17 February 2020

volume

22

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17 February 2020

page(s)

668-684

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17 February 2020

issue

4

1 reference

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Spinal muscular atrophy: a clinical and research update

17 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

21 January 2018

Spinal muscular atrophy

1 reference

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Is spinal muscular atrophy the result of defects in motor neuron processes?

21 January 2018

1 reference

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Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

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The survival motor neuron protein in spinal muscular atrophy

21 January 2018

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Correlation between severity and SMN protein level in spinal muscular atrophy

21 January 2018

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Molecular functions of the SMN complex

21 January 2018

1 reference

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Chaperoning ribonucleoprotein biogenesis in health and disease

21 January 2018

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Biogenesis of spliceosomal small nuclear ribonucleoproteins

21 January 2018

1 reference

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SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing

21 January 2018

1 reference

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A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy

21 January 2018

1 reference

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Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy

21 January 2018

1 reference

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Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs

21 January 2018

1 reference

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A feedback loop regulates splicing of the spinal muscular atrophy-modifying gene, SMN2.

21 January 2018

1 reference

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Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The COPI vesicle complex binds and moves with survival motor neuron within axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Neuronal RNA granules: movers and makers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

RNA granules: the good, the bad and the ugly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Local RNA translation at the synapse and in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Exercise-induced activation of NMDA receptor promotes motor unit development and survival in a type 2 spinal muscular atrophy model mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Embryonic motor axon development in the severe SMA mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The SMN complex, an assemblyosome of ribonucleoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Inducers of erythroleukemic differentiation cause messenger RNAs that lack poly(A)-binding protein to accumulate in translationally inactive, salt-labile 80 S ribosomal complexes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Ordered cooperative functions of PRMT1, p300, and CARM1 in transcriptional activation by p53

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Arginine methylation an emerging regulator of protein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Arginine methyltransferase CARM1 is a promoter-specific regulator of NF-kappaB-dependent gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Minireview: protein arginine methylation of nonhistone proteins in transcriptional regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Regulated recruitment of tumor suppressor BRCA1 to the p21 gene by coactivator methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The arginine methyltransferase CARM1 regulates the coupling of transcription and mRNA processing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Automethylation of CARM1 allows coupling of transcription and mRNA splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Gemin5 delivers snRNA precursors to the SMN complex for snRNP biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The Gemin5 protein of the SMN complex identifies snRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Analysis of SMN-neurite granules: Core Cajal body components are absent from SMN-cytoplasmic complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

SMN and Gemins: 'we are family' … or are we?: insights into the partnership between Gemins and the spinal muscular atrophy disease protein SMN.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

miRNP:mRNA association in polyribosomes in a human neuronal cell line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

miRNPs: a novel class of ribonucleoproteins containing numerous microRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

A novel role for Gemin5 in mRNA translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Identification of gemin5 as a novel 7-methylguanosine cap-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Quantitative proteomics identifies Gemin5, a scaffolding protein involved in ribonucleoprotein assembly, as a novel partner for eukaryotic initiation factor 4E

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Tudor domains bind symmetrical dimethylated arginines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Structural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

New perspectives on the biology of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Cytoplasmic RNA-binding proteins and the control of complex brain function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Symmetrical dimethylation of arginine residues in spliceosomal Sm protein B/B' and the Sm-like protein LSm4, and their interaction with the SMN protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Toward an assembly line for U7 snRNPs: interactions of U7-specific Lsm proteins with PRMT5 and SMN complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Eukaryotic Lsm proteins: lessons from bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

LSm proteins form heptameric rings that bind to RNA via repeating motifs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

LSm1-7 complexes bind to specific sites in viral RNA genomes and regulate their translation and replication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

RAP55, a cytoplasmic mRNP component, represses translation in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

SMN interacts with a novel family of hnRNP and spliceosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Survival motor neuron protein facilitates assembly of stress granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Protein expression changes in spinal muscular atrophy revealed with a novel antibody array technology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Proteomic assessment of a cell model of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Survival motor neuron affects plastin 3 protein levels leading to motor defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Laminin induced local axonal translation of β-actin mRNA is impaired in SMN-deficient motoneurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

CARM1 regulates proliferation of PC12 cells by methylating HuD

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

CARM1 is required in embryonic stem cells to maintain pluripotency and resist differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Arginine methyltransferase CARM1/PRMT4 regulates endochondral ossification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Sirtuin 1 regulation of developmental genes during differentiation of stem cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Early functional impairment of sensory-motor connectivity in a mouse model of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Site-directed mutagenesis by overlap extension using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Cotranscriptional exon skipping in the genotoxic stress response

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Regulation of H-ras splice variant expression by cross talk between the p53 and nonsense-mediated mRNA decay pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Antibodies to small nuclear RNAs complexed with proteins are produced by patients with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Cotranscriptional splicing potentiates the mRNA production from a subset of estradiol-stimulated genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Animal models of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS474

21 January 2018

Identifiers

DOI

10.1093/HMG/DDS474

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23136128%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

1 reference