Evidence map›Paper›PMID 25074806›Full record

ArticleJournal of cell science2014

p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation.

Moonsup Lee, Hong Ji, Yasuhide Furuta, Jae-il Park, Pierre D McCrea

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  14. Functional roles of p120ctn family of proteins in central neurons.Seminars in cell & developmental biology · 2017
    Review
  15. A central role for cadherin signaling in cancer.Experimental cell research · 2017
    Review
  16. Article
  17. Article
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  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

5 authors at 2 institutions in 2 countries.

Moonsup LeeDepartment of Biochemistry and Molecular Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA Program in Genes and Development, The University of Texas Graduate School of Biomedical Science-Houston, Houston, TX 77030, USA.
Hong JiDepartment of Biochemistry and Molecular Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Yasuhide FurutaLaboratory for Animal Resources and Genetic Engineering, Riken Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.
Jae-il ParkDepartment of Experimental Radiation Oncology, Division of Radiation Oncology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.
Pierre D McCreaDepartment of Biochemistry and Molecular Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA Program in Genes and Development, The University of Texas Graduate School of Biomedical Science-Houston, Houston, TX 77030, USA pdmccrea@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USGenetic Resources Center · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
p120-catenin sub-family functionsR01GM052112 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCREA, PIERRE D · 1995 to 2010
$3.5M
Nuclear functions of catenin subfamiliesR01GM107079 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCREA, PIERRE D · 2014 to 2017
$1.8M
NCI NIH HHS CA-16672NCI NIH HHS P30 CA016672NIGMS NIH HHS R01 GM052112NIGMS NIH HHS R01 GM107079NIGMS NIH HHS R01 GM52112
6 · The paper itself

Abstract

Although the canonical Wnt pathway and β-catenin have been extensively studied, less is known about the role of p120-catenin (also known as δ1-catenin) in the nuclear compartment. Here, we report that p120-catenin binds and negatively regulates REST and CoREST (also known as Rcor1), a repressive transcriptional complex that has diverse developmental and pathological roles. Using mouse embryonic stem cells (mESCs), mammalian cell lines, Xenopus embryos and in vitro systems, we find that p120-catenin directly binds the REST-CoREST complex, displacing it from established gene targets to permit their transcriptional activation. Importantly, p120-catenin levels further modulate the mRNA and protein levels of Oct4 (also known as POU5F1), Nanog and Sox2, and have an impact upon the differentiation of mESCs towards neural fates. In assessing potential upstream inputs to this new p120-catenin-REST-CoREST pathway, REST gene targets were found to respond to the level of E-cadherin, with evidence suggesting that p120-catenin transduces signals between E-cadherin and the nucleus. In summary, we provide the first evidence for a direct upstream modulator and/or pathway regulating REST-CoREST, and reveal a substantial role for p120-catenin in the modulation of stem cell differentiation.

Indexed as

Cell DifferentiationAnimalsCateninsCo-Repressor ProteinsDelta CateninEmbryonic Stem CellsHumansMiceNerve Tissue ProteinsOctamer Transcription Factor-3RE1-Silencing Transcription FactorRepressor ProteinsXenopus laevisCateninsCo-Repressor ProteinsDelta CateninNerve Tissue ProteinsOctamer Transcription Factor-3Pou5f1 protein, mouseRcor2 protein, mouseRE1-Silencing Transcription FactorRepressor ProteinsCoRESTE-cadherinMouse embryonic stem cellp120-cateninREST

Identifiers

PMID25074806
PMCPMC4163646
OpenAlexW2097713262

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.