Evidence map›Paper›PMID 15684034›Full record

ArticleThe Journal of cell biology2005

Receptor tyrosine phosphatase-dependent cytoskeletal remodeling by the hedgehog-responsive gene MIM/BEG4.

Rosa Gonzalez-Quevedo, Marina Shoffer, Lily Horng, Anthony E Oro

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

  1. MTSS1: beyond the integration of actin and membrane dynamics.Cellular and molecular life sciences : CMLS · 2024
    Review
  2. Article
  3. Article
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  5. Article
  6. MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  7. Article
  8. Deciphering the BAR code of membrane modulators.Cellular and molecular life sciences : CMLS · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. MTSS1 overexpression correlates with poor prognosis in colorectal cancer.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2011
    Article
  15. Article
  16. MIM regulates vertebrate neural tube closure.Development (Cambridge, England) · 2011
    Article
  17. Article
  18. Article
  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 1 institution in 1 country.

Rosa Gonzalez-QuevedoProgram in Epithelial Biology, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Marina Shoffer
Lily Horng
Anthony E Oro
Stanford University · US

Funding

Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Transposon based gene therapeuticsP01AR044012 · NIAMS · STANFORD UNIVERSITY · PI MARINKOVICH, MATT PETER · 1997 to 2006
$10.2M
STROMAL REGULATION OF BASAL CELL CARCINOMA FORMATIONR01AR046786 · NIAMS · STANFORD UNIVERSITY · PI Anthony E Oro · 2001 to 2026
$9.5M
NIAMS NIH HHS AR046786NIAMS NIH HHS P01 AR044012NIAMS NIH HHS P01AR44012NIAMS NIH HHS R01 AR046786
6 · The paper itself

Abstract

During development, dynamic remodeling of the actin cytoskeleton allows the precise placement and morphology of tissues. Morphogens such as Sonic hedgehog (Shh) and local cues such as receptor protein tyrosine phosphatases (RPTPs) mediate this process, but how they regulate the cytoskeleton is poorly understood. We previously identified Basal cell carcinoma-enriched gene 4 (BEG4)/Missing in Metastasis (MIM), a Shh-inducible, Wiskott-Aldrich homology 2 domain-containing protein that potentiates Gli transcription (Callahan, C.A., T. Ofstad, L. Horng, J.K. Wang, H.H. Zhen, P.A. Coulombe, and A.E. Oro. 2004. Genes Dev. 18:2724-2729). Here, we show that endogenous MIM is induced in a patched1-dependent manner and regulates the actin cytoskeleton. MIM functions by bundling F-actin, a process that requires self-association but is independent of G-actin binding. Cytoskeletal remodeling requires an activation domain distinct from sequences required for bundling in vitro. This domain associates with RPTPdelta and, in turn, enhances RPTPdelta membrane localization. MIM-dependent cytoskeletal changes can be inhibited using a soluble RPTPdelta-D2 domain. Our data suggest that the hedgehog-responsive gene MIM cooperates with RPTP to induce cytoskeletal changes.

Indexed as

ActinsAnimalsBinding SitesCell LineCell Line, TumorCell Surface ExtensionsCytoskeletonEpithelial CellsFibroblastsFocal AdhesionsGAP-43 ProteinGene ExpressionHomeodomain ProteinsImmunohistochemistryIntracellular Signaling Peptides and ProteinsLIM-Homeodomain ProteinsActinsGAP-43 ProteinHomeodomain Proteinsinsulin gene enhancer binding protein Isl-1Intracellular Signaling Peptides and ProteinsLIM-Homeodomain ProteinsMembrane ProteinsMicrofilament ProteinsMtss1 protein, mouseNeoplasm ProteinsNerve Tissue ProteinsPatched-1 ReceptorPatched ReceptorsPhosphatidylinositol 4,5-DiphosphateProteinsProtein Tyrosine PhosphatasesPtch1 protein, mousePtch1 protein, ratPtprd protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 2Receptors, Cell SurfaceTranscription FactorsVanadates

Identifiers

PMID15684034
PMCPMC2171717
OpenAlexW1983797468

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.