Evidence map›Paper›PMID 22275148›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2012

Developmental expression of Drosophila Wiskott-Aldrich Syndrome family proteins.

Evelyn Rodriguez-Mesa, Maria Teresa Abreu-Blanco, Alicia E Rosales-Nieves, Susan M Parkhurst

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Actomyosin contraction in the follicular epithelium provides the major mechanical force for follicle rupture duringProceedings of the National Academy of Sciences of the United States of America · 2024
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  11. Journal of cell science · 2020
    Article
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  15. Real-time insights into regulated exocytosis.Journal of cell science · 2017
    Review
  16. Coordinated autoinhibition of F-BAR domain membrane binding and WASp activation by Nervous Wreck.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  17. Article
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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

4 authors at 2 institutions in 3 countries.

Evelyn Rodriguez-MesaDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
Maria Teresa Abreu-Blanco
Alicia E Rosales-Nieves
Susan M Parkhurst
Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAFred Hutch Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Regulation of Membrane-Cortical Cytoskeleton Crosstalk by WASHR01GM097083 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PARKHURST, SUSAN M · 2011 to 2014
$1.4M
NCI NIH HHS P30 CA015704NIGMS NIH HHS GM097083NIGMS NIH HHS R01 GM097083
6 · The paper itself

Abstract

backgroundWiskott-Aldrich Syndrome (WASP) family proteins participate in many cellular processes involving rearrangements of the actin cytoskeleton. To the date, four WASP subfamily members have been described in Drosophila: Wash, WASp, SCAR, and Whamy. Wash, WASp, and SCAR are essential during early Drosophila development where they function in orchestrating cytoplasmic events including membrane-cytoskeleton interactions. A mutant for Whamy has not yet been reported.

resultsWe generated monoclonal antibodies that are specific to Drosophila Wash, WASp, SCAR, and Whamy, and use these to describe their spatial and temporal localization patterns. Consistent with the importance of WASP family proteins in flies, we find that Wash, WASp, SCAR, and Whamy are dynamically expressed throughout oogenesis and embryogenesis. For example, we find that Wash accumulates at the oocyte cortex. WASp is highly expressed in the PNS, while SCAR is the most abundantly expressed in the CNS. Whamy exhibits an asymmetric subcellular localization that overlaps with mitochondria and is highly expressed in muscle.

conclusionsAll four WASP family members show specific expression patterns, some of which reflect their previously known roles and others revealing new potential functions. The monoclonal antibodies developed offer valuable new tools to investigate how WASP family proteins regulate actin cytoskeleton dynamics.

Indexed as

AnimalsAntibodies, MonoclonalDrosophila melanogasterDrosophila ProteinsEmbryonic DevelopmentMicrofilament ProteinsOogenesisVesicular Transport ProteinsWiskott-Aldrich SyndromeWiskott-Aldrich Syndrome ProteinAntibodies, MonoclonalDrosophila ProteinsMicrofilament ProteinsSCAR protein, DrosophilaVesicular Transport ProteinsWASH protein, DrosophilaWASp protein, DrosophilaWhamy protein, DrosophilaWiskott-Aldrich Syndrome Protein

Identifiers

PMID22275148
PMCPMC3288701
OpenAlexW2086653107

What OpenQuestion holds

Textmetadata
LicenceTDM
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.