Evidence map›Paper›PMID 12070130›Full record

ArticleThe Journal of cell biology2002

Functional binding interaction identified between the axonal CAM L1 and members of the ERM family.

Tracey C Dickson, C David Mintz, Deanna L Benson, Stephen R J Salton

Erratum issuedOpen 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. An erratum has been issued. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Neuronal immunoglobulin superfamily cell adhesion molecules in epithelial morphogenesis: insights fromPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Revisiting Netrin-1: One Who Guides (Axons).Frontiers in cellular neuroscience · 2018
    Review
  10. The Pleiotropic Role of L1CAM in Tumor Vasculature.International journal of molecular sciences · 2017
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Tracey C DicksonFishberg Research Center for Neurobiology, The Mount Sinai School of Medicine, New York, NY 10029, USA.
C David Mintz
Deanna L Benson
Stephen R J Salton
Icahn School of Medicine at Mount Sinai · US

Funding

L1 function and sensitivity to ethanolR01AA014898 · NIAAA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BENSON, DEANNA L · 2005 to 2009
$1.9M
CAM TARGETING /SIGNALING--FETAL ALCOHOL SYNDROME MODEL?R21AA012971 · NIAAA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BENSON, DEANNA L · 2001 to 2003
$509k
CONFOCAL MICROSCOPE FACILITYS10RR009145 · NCRR · MOUNT SINAI SCHOOL OF MEDICINE OF CUNY · PI MASUR, SANDRA K · 1994 to 1994
–
NCRR NIH HHS S10 RR0 9145NIAAA NIH HHS AA12971NIAAA NIH HHS R01 AA014898NIAAA NIH HHS R21 AA012971
6 · The paper itself

Abstract

A yeast two-hybrid library was screened using the cytoplasmic domain of the axonal cell adhesion molecule L1 to identify binding partners that may be involved in the regulation of L1 function. The intracellular domain of L1 bound to ezrin, a member of the ezrin, radixin, and moesin (ERM) family of membrane-cytoskeleton linking proteins, at a site overlapping that for AP2, a clathrin adaptor. Binding of bacterial fusion proteins confirmed this interaction. To determine whether ERM proteins interact with L1 in vivo, extracellular antibodies to L1 were used to force cluster the protein on cultured hippocampal neurons and PC12 cells, which were then immunolabeled for ERM proteins. Confocal analysis revealed a precise pattern of codistribution between ERMs and L1 clusters in axons and PC12 neurites, whereas ERMs in dendrites and spectrin labeling remained evenly distributed. Transfection of hippocampal neurons grown on an L1 substrate with a dominant negative ERM construct resulted in extensive and abnormal elaboration of membrane protrusions and an increase in axon branching, highlighting the importance of the ERM-actin interaction in axon development. Together, our data indicate that L1 binds directly to members of the ERM family and suggest this association may coordinate aspects of axonal morphogenesis.

Indexed as

ActinsAdaptor Protein Complex 2Adaptor Proteins, Vesicular TransportAmino Acid SubstitutionAnimalsAnkyrinsAntigens, SurfaceCarrier ProteinsCell Adhesion MoleculesCell DifferentiationCytoplasmCytoskeletal ProteinsDNA-Binding ProteinsEzrinHippocampusHumansActinsAdaptor Protein Complex 2Adaptor Proteins, Vesicular TransportANK2 protein, humanAnk2 protein, ratAnkyrinsAntigens, SurfaceCarrier ProteinsCell Adhesion MoleculesCytoskeletal ProteinsDNA-Binding ProteinsETV5 protein, humanEtv5 protein, ratEzrinLeukocyte L1 Antigen ComplexMembrane GlycoproteinsMembrane ProteinsNeural Cell Adhesion MoleculesPhosphoproteinsTranscription Factors

Identifiers

PMID12070130
PMCPMC2173555
OpenAlexW2044648154

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.