Evidence map›Paper›PMID 31160712›Full record

ArticleNature cell biology2019

A single-cell transcriptional roadmap for cardiopharyngeal fate diversification.

Wei Wang, Xiang Niu, Tim Stuart, Estelle Jullian, William M Mauck, Robert G Kelly, Rahul Satija, Lionel Christiaen

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 139 citations in OpenAlex.

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  17. Cardiac Progenitor Cells of the First and Second Heart Fields.Advances in experimental medicine and biology · 2024
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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

8 authors at 4 institutions in 2 countries.

Wei WangCenter for Developmental Genetics, Department of Biology, New York University, New York, NY, USA.
Xiang NiuCenter for Genomics and Systems Biology, Department of Biology, New York University, New York, NY, USA.
Tim StuartNew York Genome Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-3044-0897
Estelle JullianAix-Marseille University, CNRS UMR 7288, Developmental Biology Institute of Marseille, Marseille, France.
William M MauckNew York Genome Center, New York, NY, USA.
Robert G KellyAix-Marseille University, CNRS UMR 7288, Developmental Biology Institute of Marseille, Marseille, France.
Rahul SatijaCenter for Genomics and Systems Biology, Department of Biology, New York University, New York, NY, USA. rsatija@nygenome.org.ORCID http://orcid.org/0000-0001-9448-8833
Lionel ChristiaenCenter for Developmental Genetics, Department of Biology, New York University, New York, NY, USA. lc121@nyu.edu.ORCID http://orcid.org/0000-0001-5930-5667
New York Genome Center · USCentre National de la Recherche Scientifique · FRNew York University · USCornell University · US

Funding

Regulation of muscle fate specification and cell migration in cardiogenic lineageR01HL108643 · NHLBI · NEW YORK UNIVERSITY · PI MOGILNER, ALEXANDER · 2011 to 2023
$5.4M
Modeling Gene Regulatory Networks for Early Cardiopharyngeal DevelopmentR01HD096770 · NICHD · NEW YORK UNIVERSITY · PI BONNEAU, RICHARD A, CHRISTIAEN, LIONEL · 2018 to 2022
$3.0M
Learning the metadata of the cell with single cell genomicsDP2HG009623 · NHGRI · NEW YORK GENOME CENTER · PI SATIJA, RAHUL · 2016 to 2016
$2.8M
NHGRI NIH HHS DP2 HG009623NHLBI NIH HHS R01 HL108643NICHD NIH HHS R01 HD096770
6 · The paper itself

Abstract

In vertebrates, multipotent progenitors located in the pharyngeal mesoderm form cardiomyocytes and branchiomeric head muscles, but the dynamic gene expression programmes and mechanisms underlying cardiopharyngeal multipotency and heart versus head muscle fate choices remain elusive. Here, we used single-cell genomics in the simple chordate model Ciona to reconstruct developmental trajectories forming first and second heart lineages and pharyngeal muscle precursors and characterize the molecular underpinnings of cardiopharyngeal fate choices. We show that FGF-MAPK signalling maintains multipotency and promotes the pharyngeal muscle fate, whereas signal termination permits the deployment of a pan-cardiac programme, shared by the first and second heart lineages, to define heart identity. In the second heart lineage, a Tbx1/10-Dach pathway actively suppresses the first heart lineage programme, conditioning later cell diversity in the beating heart. Finally, cross-species comparisons between Ciona and the mouse evoke the deep evolutionary origins of cardiopharyngeal networks in chordates.

Indexed as

AnimalsCell DifferentiationCell LineageCiona intestinalisFibroblast Growth FactorsGene Expression Regulation, DevelopmentalGenomicsHeartMesodermMiceMitogen-Activated Protein Kinase KinasesMuscle, SkeletalMyocytes, CardiacPharyngeal MusclesT-Box Domain ProteinsTranscription FactorsFibroblast Growth FactorsMitogen-Activated Protein Kinase KinasesT-Box Domain ProteinsTranscription Factors

Identifiers

PMID31160712
PMCPMC7491489
OpenAlexW2950644286

What OpenQuestion holds

Textmetadata
LicenceTDM
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.