Evidence map›Paper›PMID 29777776›Full record

ArticleMechanisms of development2018

Distinct roles for the cell adhesion molecule Contactin2 in the development and function of neural circuits in zebrafish.

Suman Gurung, Emilia Asante, Devynn Hummel, Ashley Williams, Oren Feldman-Schultz, Mary C Halloran, Vinoth Sittaramane, Anand Chandrasekhar

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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  8. Conserved and diverged asymmetric gene expression in the brain of teleosts.Frontiers in cell and developmental biology · 2022
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  11. 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

8 authors at 3 institutions in 1 country.

Suman GurungDivision of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Emilia AsanteDivision of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Devynn HummelDivision of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Ashley WilliamsDepartment of Biology, Georgia Southern University, Statesboro, GA 30458, USA.
Oren Feldman-SchultzDepartment of Integrative Biology, Department of Neuroscience, University of Wisconsin, Madison, WI 53706, USA.
Mary C HalloranDepartment of Integrative Biology, Department of Neuroscience, University of Wisconsin, Madison, WI 53706, USA.
Vinoth SittaramaneDepartment of Biology, Georgia Southern University, Statesboro, GA 30458, USA.
Anand ChandrasekharDivision of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA. Electronic address: AnandC@missouri.edu.
University of Missouri · USGeorgia Southern University · USUniversity of Wisconsin–Madison · US

Funding

Development of Cranial Motor NeuronsR01NS040449 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHANDRASEKHAR, ANAND · 2001 to 2011
$2.3M
Regulation of protein targeting in axon guidance and neuronal morphogenesisR01NS086934 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 2015 to 2018
$1.3M
NINDS NIH HHS R01 NS040449NINDS NIH HHS R01 NS086934
6 · The paper itself

Abstract

Contactin2 (Cntn2)/Transient Axonal Glycoprotein 1 (Tag1), a neural cell adhesion molecule, has established roles in neuronal migration and axon fasciculation in chick and mouse. In zebrafish, antisense morpholino-based studies have indicated roles for cntn2 in the migration of facial branchiomotor (FBM) neurons, the guidance of the axons of the nucleus of the medial longitudinal fascicle (nucMLF), and the outgrowth of Rohon-Beard (RB) central axons. To study functions of Cntn2 in later stages of neuronal development, we generated cntn2 mutant zebrafish using CRISPR-Cas9. Using a null mutant allele, we detected genetic interactions between cntn2 and the planar cell polarity gene vangl2, as shown previously with cntn2 morphants, demonstrating a function for cntn2 during FBM neuron migration in a sensitized background of reduced planar cell polarity signaling. In addition, maternal-zygotic (MZ) cntn2 mutant larvae exhibited aberrant touch responses and swimming, suggestive of defects in sensorimotor circuits, consistent with studies in mice. However, the nucMLF axon convergence, FBM neuron migration, and RB outgrowth defects seen in morphants were not seen in the mutants, and we show here that they are likely off-target effects of morpholinos. However, MLF axons exhibited local defasciculation in MZcntn2 mutants, consistent with a role for Cntn2 in axon fasciculation. These data demonstrate distinct roles for zebrafish cntn2 in neuronal migration and axon fasciculation, and in the function of sensorimotor circuits.

Indexed as

AnimalsAxonsCell AdhesionCell MovementCell PolarityContactin 2CRISPR-Cas SystemsGene Expression Regulation, DevelopmentalHumansMiceMorpholinosMotor NeuronsNeurogenesisZebrafishZebrafish Proteinscntn2 protein, zebrafishContactin 2MorpholinosZebrafish ProteinsAxon guidanceCell adhesion moleculeCntn2CRISPR/Cas9Facial branchiomotor neuronMorpholinoNeuronal migrationnucMLFVangl2Zebrafish

Identifiers

PMID29777776
PMCPMC8276388
OpenAlexW2804802811

What OpenQuestion holds

Textmetadata
LicenceTDM
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.