Evidence map›Paper›PMID 25002511›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Genetic evidence that Celsr3 and Celsr2, together with Fzd3, regulate forebrain wiring in a Vangl-independent manner.

Yibo Qu, Yuhua Huang, Jia Feng, Gonzalo Alvarez-Bolado, Elizabeth A Grove, Yingzi Yang, Fadel Tissir, Libing Zhou, Andre M Goffinet

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 84 citations in OpenAlex.

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  6. Identification of novel genetic loci and candidate genes for progressive ethanol consumption in diversity outbred mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  18. Early construction of the thalamocortical axon pathway requires c-Jun N-terminal kinase signaling within the ventral forebrain.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  19. The Immunoglobulin Superfamily MembersJournal of developmental biology · 2022
    Article
  20. 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

9 authors at 6 institutions in 5 countries.

Yibo QuGuangdong-Hong Kong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou 510632, China;
Yuhua HuangGuangdong-Hong Kong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou 510632, China;
Jia FengGuangdong-Hong Kong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou 510632, China;
Gonzalo Alvarez-BoladoDepartment of Neuroanatomy, Heidelberg University, D-69120 Heidelberg, Germany;
Elizabeth A GroveNeuroscience, The University of Chicago, Chicago, IL 60637;
Yingzi YangNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892;
Fadel TissirWELBIO - Walloon Excellence in Life Sciences and Biotechnology and Institute of Neuroscience, University of Louvain, B1200 Brussels, Belgium; and.
Libing ZhouGuangdong-Hong Kong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou 510632, China;State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong andre.goffinet@uclouvain.be tlibingzh@jnu.edu.cn.
Andre M GoffinetWELBIO - Walloon Excellence in Life Sciences and Biotechnology and Institute of Neuroscience, University of Louvain, B1200 Brussels, Belgium; and andre.goffinet@uclouvain.be tlibingzh@jnu.edu.cn.
Jinan University · CNWalloon Excellence in Lifesciences and Biotechnology · BEHeidelberg University · DENational Human Genome Research Institute · USUniversity of Chicago · USUniversity of Hong Kong · HK

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Wnt signaling in vetebrate limb and skeletal developmentZIAHG000187 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI YANG, YINGZI · 2009 to 2015
$7.1M
NCATS NIH HHS UL1 TR000430
6 · The paper itself

Abstract

Celsr3 and Fzd3, members of "core planar cell polarity" (PCP) genes, were shown previously to control forebrain axon guidance and wiring by acting in axons and/or guidepost cells. Here, we show that Celsr2 acts redundantly with Celsr3, and that their combined mutation mimics that of Fzd3. The phenotypes generated upon inactivation of Fzd3 in different forebrain compartments are similar to those in conditional Celsr2-3 mutants, indicating that Fzd3 and Celsr2-3 act in the same population of cells. Inactivation of Celsr2-3 or Fzd3 in thalamus does not affect forebrain wiring, and joint inactivation in cortex and thalamus adds little to cortical inactivation alone in terms of thalamocortical projections. On the other hand, joint inactivation perturbs strongly the formation of the barrel field, which is unaffected upon single cortical or thalamic inactivation, indicating a role for interactions between thalamic axons and cortical neurons in cortical arealization. Unexpectedly, forebrain wiring is normal in mice defective in Vangl1 and Vangl2, showing that, contrary to epithelial PCP, axon guidance can be Vangl independent in some contexts. Our results suggest that Celsr2-3 and Fzd3 regulate axonal navigation in the forebrain by using mechanisms different from classical epithelial PCP, and require interacting partners other than Vangl1-2 that remain to be identified.

Indexed as

AnimalsAxonsCadherinsCarrier ProteinsCerebral CortexFrizzled ReceptorsGene SilencingIntegrasesMembrane ProteinsMiceMutationNerve NetNerve Tissue ProteinsPhenotypeProsencephalonReceptors, Cell SurfaceCadherinsCarrier ProteinsCelsr2 protein, mouseCelsr3 protein, mouseCre recombinaseFrizzled ReceptorsFzd3 protein, mouseIntegrasesLtap protein, mouseMembrane ProteinsNerve Tissue ProteinsReceptors, Cell SurfaceVangl1 protein, mouseanterior commissurecortical barrelsCreinternal capsule

Identifiers

PMID25002511
PMCPMC4115502
OpenAlexW1968100682

What OpenQuestion holds

Textmetadata
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.