Evidence map›Paper›PMID 12499361›Full record

ArticleThe Journal of cell biology2002

SadA, a novel adhesion receptor in Dictyostelium.

Petra Fey, Stephen Stephens, Margaret A Titus, Rex L Chisholm

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

58 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Article
  3. Reduced cell-substrate adhesion formation promotes cell migration inbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Procedures to Measure Dictyostelium Phagocytosis and Macropinocytosis.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  7. Article
  8. Review
  9. Adhesion ofFrontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Harnessing Motile Amoeboid Cells as Trucks for Microtransport and -Assembly.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  16. Article
  17. Shear force-based genetic screen reveals negative regulators of cell adhesion and protrusive activity.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  18. Eat Prey, Live:Frontiers in immunology · 2017
    Review
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Petra FeyDepartment of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611, USA.
Stephen Stephens
Margaret A Titus
Rex L Chisholm
Northwestern University · USUniversity of Minnesota · US

Funding

MOLECULAR GENETIC ANALYSIS OF MOTILITY: MYOSIN LCSR01GM039264 · NIGMS · NORTHWESTERN UNIVERSITY · PI CHISHOLM, REX L · 1988 to 2002
$1.0M
NIGMS NIH HHS GM39264NIGMS NIH HHS R01 GM039264
6 · The paper itself

Abstract

Little is known about cell-substrate adhesion and how motile and adhesive forces work together in moving cells. The ability to rapidly screen a large number of insertional mutants prompted us to perform a genetic screen in Dictyostelium to isolate adhesion-deficient mutants. The resulting substrate adhesion-deficient (sad) mutants grew in plastic dishes without attaching to the substrate. The cells were often larger than their wild-type parents and displayed a rough surface with many apparent blebs. One of these mutants, sadA-, completely lacked substrate adhesion in growth medium. The sadA- mutant also showed slightly impaired cytokinesis, an aberrant F-actin organization, and a phagocytosis defect. Deletion of the sadA gene by homologous recombination recreated the original mutant phenotype. Expression of sadA-GFP in sadA-null cells restored the wild-type phenotype. In sadA-GFP-rescued mutant cells, sadA-GFP localized to the cell surface, appropriate for an adhesion molecule. SadA contains nine putative transmembrane domains and three conserved EGF-like repeats in a predicted extracellular domain. The EGF repeats are similar to corresponding regions in proteins known to be involved in adhesion, such as tenascins and integrins. Our data combined suggest that sadA is the first substrate adhesion receptor to be identified in Dictyostelium.

Indexed as

ActinsAnimalsBlotting, NorthernCell AdhesionCell Adhesion MoleculesChickensCloning, MolecularDictyosteliumDNA, ComplementaryEpidermal Growth FactorFlow CytometryGene DeletionGreen Fluorescent ProteinsLuminescent ProteinsMicroscopy, FluorescenceModels, BiologicalActinsCell Adhesion MoleculesDNA, ComplementaryEpidermal Growth FactorGreen Fluorescent ProteinsLuminescent ProteinsTenascin

Identifiers

PMID12499361
PMCPMC2173991
OpenAlexW2140831067

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.