Evidence map›Paper›PMID 26004184›Full record

ArticleCell reports2015

The Adhesion Molecule KAL-1/anosmin-1 Regulates Neurite Branching through a SAX-7/L1CAM-EGL-15/FGFR Receptor Complex.

Carlos A Díaz-Balzac, María I Lázaro-Peña, Gibram A Ramos-Ortiz, Hannes E Bülow

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

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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 2 countries.

Carlos A Díaz-BalzacDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
María I Lázaro-PeñaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Gibram A Ramos-OrtizDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Biology, University of Puerto Rico-Río Piedras, San Juan 00931, Puerto Rico.
Hannes E BülowDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: hannes.buelow@einstein.yu.edu.
Albert Einstein College of Medicine · USUniversity of Puerto Rico at Río Piedras · PR

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Support for the Rose F. Kennedy IDDRCU54HD090260 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MOLHOLM, SOPHIE, WALKLEY, STEVEN UPSHAW · 2016 to 2020
$6.0M
Translational Neuroimaging CoreP30HD071593 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WALKLEY, STEVEN UPSHAW · 2011 to 2015
$5.6M
Genetic Analysis of Kallmann Syndrome in C. elegansR01HD055380 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUELOW, HANNES ERICH · 2008 to 2012
$1.9M
Genetic Analyses of Heparan Sulfate Function in Cell-Cell InteractionsR01GM101313 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BUELOW, HANNES ERICH · 2013 to 2016
$1.3M
Identification of Novel Loci Interacting with the Kallmann Syndrome Gene Kal-1F31HD066967 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DIAZ-BALZAC, CARLOS ANTONIO · 2010 to 2013
$168k
NICHD NIH HHS F31 HD066967NICHD NIH HHS F31HD066967NICHD NIH HHS P30 HD071593NICHD NIH HHS P30HD071593NICHD NIH HHS R01 HD055380NICHD NIH HHS R01HD055380NICHD NIH HHS U54 HD090260NIGMS NIH HHS R01 GM101313NIGMS NIH HHS R01GM101313NIGMS NIH HHS T32 GM007288NIGMS NIH HHS T32GM007288NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32GM07491NIH HHS P40 OD010440
6 · The paper itself

Abstract

Neurite branching is essential for correct assembly of neural circuits, yet it remains a poorly understood process. For example, the neural cell adhesion molecule KAL-1/anosmin-1, which is mutated in Kallmann syndrome, regulates neurite branching through mechanisms largely unknown. Here, we show that KAL-1/anosmin-1 mediates neurite branching as an autocrine co-factor with EGL-17/FGF through a receptor complex consisting of the conserved cell adhesion molecule SAX-7/L1CAM and the fibroblast growth factor receptor EGL-15/FGFR. This protein complex, which appears conserved in humans, requires the immunoglobulin (Ig) domains of SAX-7/L1CAM and the FN(III) domains of KAL-1/anosmin-1 for formation in vitro as well as function in vivo. The kinase domain of the EGL-15/FGFR is required for branching, and genetic evidence suggests that ras-mediated signaling downstream of EGL-15/FGFR is necessary to effect branching. Our studies establish a molecular pathway that regulates neurite branching during development of the nervous system.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsHEK293 CellsHumansImmunoprecipitationNerve Tissue ProteinsNeural Cell Adhesion Molecule L1Neural Cell Adhesion MoleculesNeuritesNeurogenesisReceptors, Fibroblast Growth FactorSignal TransductionCaenorhabditis elegans ProteinsEGL-15 protein, C elegansKAL-1 protein, C elegansNerve Tissue ProteinsNeural Cell Adhesion Molecule L1Neural Cell Adhesion MoleculesReceptors, Fibroblast Growth FactorSAX-7 protein, C elegans

Identifiers

PMID26004184
PMCPMC4464948
OpenAlexW1555295693

What OpenQuestion holds

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Registered trials

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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.