Evidence map›Paper›PMID 29175910›Full record

ArticleJournal of cell science2018

PAWS1 controls cytoskeletal dynamics and cell migration through association with the SH3 adaptor CD2AP.

Timothy D Cummins, Kevin Z L Wu, Polyxeni Bozatzi, Kevin S Dingwell, Thomas J Macartney, Nicola T Wood, Joby Varghese, Robert Gourlay, David G Campbell, Alan Prescott and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 59 citations in OpenAlex.

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  10. Review
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  13. MCM3AP-AS1: An Indispensable Cancer-Related LncRNA.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Tyrosine Phosphorylation of CD2AP Affects Stability of the Slit Diaphragm Complex.Journal of the American Society of Nephrology : JASN · 2019
    Article
  18. Review
  19. PathogenicWellcome open research · 2019
    Article
  20. Review
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

13 authors at 5 institutions in 2 countries.

Timothy D CumminsMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Kevin Z L WuMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Polyxeni BozatziMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Kevin S DingwellThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Thomas J MacartneyMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Nicola T WoodMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Joby VargheseMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Robert GourlayMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
David G CampbellMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK.
Alan PrescottCell Signalling and Immunology, University of Dundee, Dundee DD1 5EH, UK.
Eric GriffisCentre for Gene Regulation and Expression, University of Dundee, Dundee DD1 5EH, UK.ORCID 0000-0002-2832-6649
James C SmithThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Gopal P SapkotaMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, Dundee DD1 5EH, UK g.sapkota@dundee.ac.uk.ORCID 0000-0001-9931-3338
MRC Protein Phosphorylation and Ubiquitylation Unit · GBThe Francis Crick Institute · GBNational Institutes of Health · USUniversity of Dundee · GBUniversity of Louisville · US

Funding

Medical Research Council FC001157Medical Research Council MC_U117597140Medical Research Council MC_UU_00018/6Medical Research Council MC_UU_12016/3Wellcome Trust FC001157
6 · The paper itself

Abstract

Our previous studies of PAWS1 (protein associated with SMAD1; also known as FAM83G) have suggested that this molecule has roles beyond BMP signalling. To investigate these roles, we have used CRISPR/Cas9 to generate PAWS1-knockout U2OS osteosarcoma cells. Here, we show that PAWS1 plays a role in the regulation of the cytoskeletal machinery, including actin and focal adhesion dynamics, and cell migration. Confocal microscopy and live cell imaging of actin in U2OS cells indicate that PAWS1 is also involved in cytoskeletal dynamics and organization. Loss of PAWS1 causes severe defects in F-actin organization and distribution as well as in lamellipodial organization, resulting in impaired cell migration. PAWS1 interacts in a dynamic fashion with the actin/cytoskeletal regulator CD2AP at lamellae, suggesting that its association with CD2AP controls actin organization and cellular migration. Genetic ablation of CD2AP from U2OS cells instigates actin and cell migration defects reminiscent of those seen in PAWS1-knockout cells.This article has an associated First Person interview with the first authors of the paper.

Indexed as

Cell MovementActin CytoskeletonActinsAdaptor Proteins, Signal TransducingCell Line, TumorCRISPR-Cas SystemsCytoskeletal ProteinsFocal AdhesionsGene Knockout TechniquesHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsSignal TransductionActinsAdaptor Proteins, Signal TransducingCD2-associated proteinCytoskeletal ProteinsFAM83G protein, humanIntracellular Signaling Peptides and ProteinsActin cytoskeletonCD2APCell migrationFAM83GPAWS1

Identifiers

PMID29175910
PMCPMC5818054
OpenAlexW2950051413

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.