The SMN complex, an assemblyosome of ribonucleoproteins (Q28204829)

ribonucleoprotein complex

Europe PubMed Central

title

The SMN complex, an assemblyosome of ribonucleoproteins (English)

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main subject

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Sergey Paushkin

1

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Amélie K Gubitz

series ordinal

2

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Séverine Massenet

series ordinal

3

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Gideon Dreyfuss

series ordinal

4

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language of work or name

English

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publication date

June 2002

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published in

Current Opinion in Cell Biology

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volume

14

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issue

3

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page(s)

305-12

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cites work

Classification of spinal muscular atrophies

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https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Spinal muscular atrophy

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7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

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7 January 2021

When is a deletion not a deletion? When it is converted

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7 January 2021

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The Schizosaccharomyces pombe protein Yab8p and a novel factor, Yip1p, share structural and functional similarity with the spinal muscular atrophy-associated proteins SMN and SIP1.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN.

1 reference

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7 January 2021

A novel nuclear structure containing the survival of motor neurons protein

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Cajal bodies: the first 100 years

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Nuclear bodies: multifaceted subdomains of the interchromatin space.

1 reference

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7 January 2021

Structure and Function in the Nucleus

1 reference

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7 January 2021

Microinjection of anti-coilin antibodies affects the structure of coiled bodies

1 reference

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7 January 2021

Human autoantibody to a novel protein of the nuclear coiled body: immunological characterization and cDNA cloning of p80-coilin

1 reference

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7 January 2021

The spinal muscular atrophy disease gene product, SMN: A link between snRNP biogenesis and the Cajal (coiled) body

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells

1 reference

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7 January 2021

Nuclear gems and Cajal (coiled) bodies in fetal tissues: nucleolar distribution of the spinal muscular atrophy protein, SMN

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Coiled bodies and gems: Janus or gemini?

1 reference

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7 January 2021

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Gemin5, a novel WD repeat protein component of the SMN complex that binds Sm proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The WD repeat: a common architecture for diverse functions

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

A role for polyproline motifs in the spinal muscular atrophy protein SMN. Profilins bind to and colocalize with smn in nuclear gems

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein

1 reference

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7 January 2021

A direct interaction between the survival motor neuron protein and p53 and its relationship to spinal muscular atrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

A functional interaction between the survival motor neuron complex and RNA polymerase II

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Methylation of Sm proteins by a complex containing PRMT5 and the putative U snRNP assembly factor pICln

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

The methylosome, a 20S complex containing JBP1 and pICln, produces dimethylarginine-modified Sm proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

A novel WD repeat protein component of the methylosome binds Sm proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

SMN oligomerization defect correlates with spinal muscular atrophy severity

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Direct interaction of the spinal muscular atrophy disease protein SMN with the small nucleolar RNA-associated protein fibrillarin

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

SMN tudor domain structure and its interaction with the Sm proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

1 reference

7 January 2021

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Sequence-specific interaction of U1 snRNA with the SMN complex

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

RNA helicase A mediates association of CBP with RNA polymerase II

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

SMN interacts with a novel family of hnRNP and spliceosomal proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

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?

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

Spliceosomal UsnRNP biogenesis, structure and function

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2802%2900332-0

7 January 2021

10.1016/S0955-0674(02)00332-0

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12067652

1 reference

Consolidated OpenCitations Corpus – April 2017