Evidence map›Paper›PMID 15332112›Full record

ArticleEMBO reports2004

A neural-specific splicing event generates an active form of the Wiskott-Aldrich syndrome protein.

Yann Le Page, Florence Demay, Gilles Salbert

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 50% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Yann Le PageEquipe 'Information et Programmation Cellulaire', UMR 6026 CNRS, Université de Rennes I, Campus de Beaulieu, 35042 Rennes Cedex, France.
Florence Demay
Gilles Salbert
Université de Rennes · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actin polymerization is required for cellular events such as podosome, lamellipode or filopode formation in migrating cells, and members of the Wiskott-Aldrich syndrome protein (WASP) family have essential roles in regulating actin dynamics at the cell leading edge. However, WASP proteins need first to be activated in order to be able to target actin polymerization. Here, we show the occurrence of a neural-specific splicing event, which is favoured by the nuclear orphan receptor chicken ovalbumin upstream promoter-transcription factor I, and generates a truncated WASP protein deleted of exon 2-encoded amino acids. This deletion relocates the protein to the plasma membrane and induces the formation of actin-rich podosome-like structures that also contain paxillin and vinculin. Furthermore, expression of the truncated protein in PC12 cells, as well as in primary neurons, stimulates neuritogenesis. These data underscore the importance of the neural-specific splicing of WASP RNA during development.

Indexed as

ActinsAlternative SplicingAnimalsChlorocebus aethiopsCOS CellsCOUP Transcription Factor IDNA-Binding ProteinsExonsGenes, ReporterMutationNeuronsPC12 CellsProtein IsoformsProteinsRatsRecombinant Fusion ProteinsActinsCOUP Transcription Factor IDNA-Binding ProteinsNr2f1 protein, ratProtein IsoformsProteinsRecombinant Fusion ProteinsTranscription FactorsWas protein, ratWiskott-Aldrich Syndrome Protein

Identifiers

PMID15332112
PMCPMC1299140
OpenAlexW2117647543

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.