Evidence map›Paper›PMID 28457792›Full record

ArticleDevelopmental cell2017

A Gene Regulatory Network Balances Neural and Mesoderm Specification during Vertebrate Trunk Development.

Mina Gouti, Julien Delile, Despina Stamataki, Filip J Wymeersch, Yali Huang, Jens Kleinjung, Valerie Wilson, James Briscoe

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 1 synthesis or guideline pooled it, 284 citations in OpenAlex.

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  13. Large-scale mouse mutagenesis identifies novel genes affecting vertebral anatomy.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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81 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 2 countries.

Mina GoutiThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK; Max Delbrück Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany. Electronic address: mina.gouti@mdc-berlin.de.
Julien DelileThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Despina StamatakiThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Filip J WymeerschMRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK.
Yali HuangMRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK.
Jens KleinjungThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Valerie WilsonMRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK.
James BriscoeThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK. Electronic address: james.briscoe@crick.ac.uk.
The Francis Crick Institute · GBMRC Centre for Regenerative Medicine · GBMax Delbrück Center · DEUniversity of Edinburgh · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J015539/1Medical Research Council MR/K011200/1Medical Research Council MR/K017047/1Wellcome Trust FC001051Wellcome Trust WT098326MA
6 · The paper itself

Abstract

Transcriptional networks, regulated by extracellular signals, control cell fate decisions and determine the size and composition of developing tissues. One example is the network controlling bipotent neuromesodermal progenitors (NMPs) that fuel embryo elongation by generating spinal cord and trunk mesoderm tissue. Here, we use single-cell transcriptomics to identify the molecular signature of NMPs and reverse engineer the mechanism that regulates their differentiation. Together with genetic perturbations, this reveals a transcriptional network that integrates opposing retinoic acid (RA) and Wnt signals to determine the rate at which cells enter and exit the NMP state. RA, produced by newly generated mesodermal cells, provides feedback that initiates NMP generation and induces neural differentiation, thereby coordinating the production of neural and mesodermal tissue. Together, the data define a regulatory network architecture that balances the generation of different cell types from bipotential progenitors in order to facilitate orderly axis elongation.

Indexed as

AnimalsBody PatterningCell DifferentiationCell LineageGene Expression Regulation, DevelopmentalGene Regulatory NetworksMesodermSpinal CordVertebratesWnt Signaling Pathwaydynamical systems modelinggene regulatory networksneuromesodermal progenitorsNMPsretinoic acidsingle-cell transcriptome analysisvertebrate development

Identifiers

PMID28457792
PMCPMC5425255
OpenAlexW2607832145

What OpenQuestion 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 OpenQuestion graph.