A functional interaction between the survival motor neuron complex and RNA polymerase II (Q24674951)

3

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author name string

B Charroux

2

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M Mann

4

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G Dreyfuss

5

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language of work or name

English

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publication date

8 January 2001

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number of pages

11

1 reference

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

inferred from page(s)

published in

Journal of Cell Biology

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volume

152

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issue

1

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page(s)

75-85

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cites work

1 reference

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Assembly of the Nuclear Transcription and Processing Machinery: Cajal Bodies (Coiled Bodies) and Transcriptosomes

7 April 2017

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A protein phosphatase functions to recycle RNA polymerase II

7 April 2017

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

7 April 2017

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Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number.

7 April 2017

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RNA helicase A is essential for normal gastrulation

7 April 2017

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

7 April 2017

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

7 April 2017

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

7 April 2017

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A novel nuclear structure containing the survival of motor neurons protein

7 April 2017

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Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels

7 April 2017

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

7 April 2017

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

7 April 2017

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

7 April 2017

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Spinal muscular atrophy

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RNA Helicase A Mediates Association of CBP with RNA Polymerase II

7 April 2017

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The C-terminal domain of RNA polymerase II couples mRNA processing to transcription

7 April 2017

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Human RNA helicase A is homologous to the maleless protein of Drosophila

7 April 2017

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Requirement for TFIIH kinase activity in transcription by RNA polymerase II

7 April 2017

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Characterization of Heterogeneous Nuclear RNA-Protein Complexes In Vivo with Monoclonal Antibodies

7 April 2017

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SR proteins: a conserved family of pre-mRNA splicing factors

7 April 2017

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7 April 2017

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Cap trimethylation of U snRNA is cytoplasmic and dependent on U snRNP protein binding

7 April 2017

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Structure and Function in the Nucleus

7 April 2017

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22 April 2017

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7 April 2017

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Identification and characterization of a spinal muscular atrophy-determining gene

7 April 2017

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RNA polymerase II and the integration of nuclear events

7 April 2017

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A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

7 April 2017

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Reversible phosphorylation of the C-terminal domain of RNA polymerase II

7 April 2017

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7 April 2017

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Macromolecular domains within the cell nucleus

7 April 2017

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Phosphorylation of RNA polymerase II C-terminal domain and transcriptional elongation

7 April 2017

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7 April 2017

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Factor required for mammalian spliceosome assembly is localized to discrete regions in the nucleus

7 April 2017

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

7 April 2017

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Like attracts like: getting RNA processing together in the nucleus

28 September 2017

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Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

28 September 2017

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

28 September 2017

1 reference

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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.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2193649

A mouse model for spinal muscular atrophy

28 September 2017

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

28 September 2017

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Coupling RNA polymerase II transcription with pre-mRNA processing

28 September 2017

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A CTD function linking transcription to splicing

28 September 2017

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

28 September 2017

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The survival motor neuron protein in spinal muscular atrophy

28 September 2017

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Correlation between severity and SMN protein level in spinal muscular atrophy

28 September 2017

1 reference

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Dynamic relocation of transcription and splicing factors dependent upon transcriptional activity

28 September 2017

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Splicing factors associate with hyperphosphorylated RNA polymerase II in the absence of pre-mRNA

28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

28 September 2017

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30 May 2018

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28 November 2018

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12 December 2020

The cellular organization of gene expression

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12 December 2020

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Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III

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Classification of spinal muscular atrophies

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Identifiers

DOI

10.1083/JCB.152.1.75

1 reference

1 reference

1 reference

PubMed publication ID

11149922

1 reference