Evidence map›Paper›PMID 24333599›Full record

ArticleMechanisms of development2014

Structural and temporal requirements of Wnt/PCP protein Vangl2 function for convergence and extension movements and facial branchiomotor neuron migration in zebrafish.

Xiufang Pan, Vinoth Sittaramane, Suman Gurung, Anand Chandrasekhar

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Gag proteins encoded by endogenous retroviruses are required for zebrafish development.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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 1 institution in 1 country.

Xiufang PanBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Vinoth SittaramaneBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Suman GurungBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Anand ChandrasekharBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA; Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA; Interdisciplinary Neuroscience Program, University of Missouri, Columbia, MO 65211, USA; Genetics Area Program, University of Missouri, Columbia, MO 65211, USA. Electronic address: AnandC@missouri.edu.
University of Missouri · US

Funding

Development of Cranial Motor NeuronsR01NS040449 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHANDRASEKHAR, ANAND · 2001 to 2011
$2.3M
Development of Cranial Motor NeuronsR56NS040449 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHANDRASEKHAR, ANAND · 2007 to 2007
$359k
NINDS NIH HHS NS040449NINDS NIH HHS R01 NS040449NINDS NIH HHS R56 NS040449
6 · The paper itself

Abstract

Van gogh-like 2 (Vangl2), a core component of the Wnt/planar cell polarity (PCP) signaling pathway, is a four-pass transmembrane protein with N-terminal and C-terminal domains located in the cytosol, and is structurally conserved from flies to mammals. In vertebrates, Vangl2 plays an essential role in convergence and extension (CE) movements during gastrulation and in facial branchiomotor (FBM) neuron migration in the hindbrain. However, the roles of specific Vangl2 domains, of membrane association, and of specific extracellular and intracellular motifs have not been examined, especially in the context of FBM neuron migration. Through heat shock-inducible expression of various Vangl2 transgenes, we found that membrane associated functions of the N-terminal and C-terminal domains of Vangl2 are involved in regulating FBM neuron migration. Importantly, through temperature shift experiments, we found that the critical period for Vangl2 function coincides with the initial stages of FBM neuron migration out of rhombomere 4. Intriguingly, we have also uncovered a putative nuclear localization motif in the C-terminal domain that may play a role in regulating CE movements.

Indexed as

AnimalsCell MembraneCell MovementFacial NerveGastrulationGene Expression Regulation, DevelopmentalIntracellular Signaling Peptides and ProteinsMembrane ProteinsMotor NeuronsProtein Structure, TertiaryRhombencephalonZebrafishIntracellular Signaling Peptides and ProteinsMembrane ProteinsVANGL2 protein, humanBranchiomotor neuronHindbrainNeuronal migrationTol2vangl2Zebrafish

Identifiers

PMID24333599
PMCPMC4116749
OpenAlexW2090851789

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.