Evidence map›Paper›PMID 27556156›Full record

ArticlePLoS genetics2016

p120 Catenin-Mediated Stabilization of E-Cadherin Is Essential for Primitive Endoderm Specification.

Tim Pieters, Steven Goossens, Lieven Haenebalcke, Vanessa Andries, Agata Stryjewska, Riet De Rycke, Kelly Lemeire, Tino Hochepied, Danny Huylebroeck, Geert Berx and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Functions of p120-catenin in physiology and diseases.Frontiers in molecular biosciences · 2024
    Review
  3. Article
  4. Journey of the mouse primitive endoderm: from specification to maturation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
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  19. Functional roles of p120ctn family of proteins in central neurons.Seminars in cell & developmental biology · 2017
    Review
  20. Article
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

15 authors at 7 institutions in 4 countries.

Tim PietersDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.ORCID 0000-0002-2958-0104
Steven GoossensDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.ORCID 0000-0002-5693-8570
Lieven HaenebalckeDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Vanessa AndriesDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.ORCID 0000-0003-4240-7098
Agata StryjewskaDepartment of Development and Regeneration, Laboratory of Molecular Biology (Celgen), University of Leuven, Leuven, Belgium.
Riet De RyckeDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Kelly LemeireDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Tino HochepiedDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.ORCID 0000-0001-5897-2054
Danny HuylebroeckDepartment of Development and Regeneration, Laboratory of Molecular Biology (Celgen), University of Leuven, Leuven, Belgium.
Geert BerxDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.ORCID 0000-0001-5770-2458
Marc P StemmlerDepartment of Molecular Embryology, Max-Planck Institute of Immunobiology, Freiburg, Germany.
Dagmar WirthHelmholtz Center for Infection Research, Braunschweig, Germany.
Jody J HaighMammalian Functional Genetics Laboratory, Division of Blood Cancers, Australian Centre for Blood Diseases, Department of Clinical Haematology, Monash University and Alfred Health Alfred Centre, Melbourne, Victoria, Australia.
Jolanda van HengelDepartment of Basic Medical Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Frans van RoyDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Ghent University · BEAlfred Health · AUErasmus MC · NLFriedrich-Alexander-Universität Erlangen-Nürnberg · DEGhent University Hospital · BEHelmholtz Centre for Infection Research · DEKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E-cadherin-mediated cell-cell adhesion is critical for naive pluripotency of cultured mouse embryonic stem cells (mESCs). E-cadherin-depleted mESC fail to downregulate their pluripotency program and are unable to initiate lineage commitment. To further explore the roles of cell adhesion molecules during mESC differentiation, we focused on p120 catenin (p120ctn). Although one key function of p120ctn is to stabilize and regulate cadherin-mediated cell-cell adhesion, it has many additional functions, including regulation of transcription and Rho GTPase activity. Here, we investigated the role of mouse p120ctn in early embryogenesis, mESC pluripotency and early fate determination. In contrast to the E-cadherin-null phenotype, p120ctn-null mESCs remained pluripotent, but their in vitro differentiation was incomplete. In particular, they failed to form cystic embryoid bodies and showed defects in primitive endoderm formation. To pinpoint the underlying mechanism, we undertook a structure-function approach. Rescue of p120ctn-null mESCs with different p120ctn wild-type and mutant expression constructs revealed that the long N-terminal domain of p120ctn and its regulatory domain for RhoA were dispensable, whereas its armadillo domain and interaction with E-cadherin were crucial for primitive endoderm formation. We conclude that p120ctn is not only an adaptor and regulator of E-cadherin, but is also indispensable for proper lineage commitment.

Indexed as

Mouse Embryonic Stem CellsAnimalsBlastocystCadherinsCateninsCell AdhesionCell DifferentiationCell LineageCell PolarityDelta CateninEmbryoid BodiesEmbryonic DevelopmentEndodermHumansMiceOptical ImagingCadherinsCateninsCdh1 protein, mouseDelta CateninrhoA GTP-Binding Protein

Identifiers

PMID27556156
PMCPMC4996431
OpenAlexW2516450226

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.