Evidence map›Paper›PMID 36154671›Full record

ArticleeLife2022

Early anteroposterior regionalisation of human neural crest is shaped by a pro-mesodermal factor.

Antigoni Gogolou, Celine Souilhol, Ilaria Granata, Filip J Wymeersch, Ichcha Manipur, Matthew Wind, Thomas J R Frith, Maria Guarini, Alessandro Bertero, Christoph Bock and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

14 authors at 8 institutions in 6 countries.

Antigoni GogolouCentre for Stem Cell Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Celine SouilholCentre for Stem Cell Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Ilaria GranataComputational and Data Science Laboratory, High Performance Computing and Networking Institute, National Research Council of Italy, Napoli, Italy.
Filip J WymeerschLaboratory for Human Organogenesis, RIKEN Center for Biosystems Dynamics Research, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Japan.ORCID 0000-0001-8999-4555
Ichcha ManipurComputational and Data Science Laboratory, High Performance Computing and Networking Institute, National Research Council of Italy, Napoli, Italy.
Matthew WindCentre for Stem Cell Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Thomas J R FrithCentre for Stem Cell Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Maria GuariniCeMM Research Center for Molecular Medicine, Austrian Academy of Sciences, Vienna, Austria.
Alessandro BerteroMolecular Biotechnology Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Christoph BockCeMM Research Center for Molecular Medicine, Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0001-6091-3088
Florian HalbritterSt. Anna Children's Cancer Research Institute, Vienna, Austria.
Minoru TakasatoLaboratory for Human Organogenesis, RIKEN Center for Biosystems Dynamics Research, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Japan.ORCID 0000-0002-0458-7414
Mario R GuarracinoUniversity of Cassino and Southern Lazio, Cassino, Italy.
Anestis TsakiridisCentre for Stem Cell Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0002-2184-2990
Neuroscience Institute · ITAustrian Academy of Sciences · ATInstitute for High Performance Computing and Networking · ITCancer Research Institute of the Slovak Academy of Sciences · SKKyoto University · JPRIKEN Center for Biosystems Dynamics Research · JPUniversità degli studi di Cassino e del Lazio Meridionale · ITUniversity of Turin · IT

Funding

Biotechnology and Biological Sciences Research Council BB/P000444/1Medical Research Council MR/V002163/1
6 · The paper itself

Abstract

The neural crest (NC) is an important multipotent embryonic cell population and its impaired specification leads to various developmental defects, often in an anteroposterior (A-P) axial level-specific manner. The mechanisms underlying the correct A-P regionalisation of human NC cells remain elusive. Recent studies have indicated that trunk NC cells, the presumed precursors of childhood tumour neuroblastoma, are derived from neuromesodermal-potent progenitors of the postcranial body. Here we employ human embryonic stem cell differentiation to define how neuromesodermal progenitor (NMP)-derived NC cells acquire a posterior axial identity. We show that TBXT, a pro-mesodermal transcription factor, mediates early posterior NC/spinal cord regionalisation together with WNT signalling effectors. This occurs by TBXT-driven chromatin remodelling via its binding in key enhancers within

Indexed as

MesodermNeural CrestCell DifferentiationHumansTranscription FactorsWnt Signaling PathwayTranscription Factorsaxial identitybrachyurydevelopmental biologyembryonic stem cellsHoxhumanmouseneural crestneuromesodermal progenitorsregenerative medicinestem cells

Identifiers

PMID36154671
PMCPMC9536837
OpenAlexW4297238864

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.