Evidence map›Paper›PMID 30721228›Full record

ArticlePLoS genetics2019

Nr2f-dependent allocation of ventricular cardiomyocyte and pharyngeal muscle progenitors.

Tracy E Dohn, Padmapriyadarshini Ravisankar, Fouley T Tirera, Kendall E Martin, Jacob T Gafranek, Tiffany B Duong, Terri L VanDyke, Melissa Touvron, Lindsey A Barske, J Gage Crump and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Atrial and Sinoatrial Node Development in the Zebrafish Heart.Journal of cardiovascular development and disease · 2021
    Review
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  14. Article
  15. Mesoderm patterning by a dynamic gradient of retinoic acid signalling.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
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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

11 authors at 2 institutions in 2 countries.

Tracy E DohnDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0001-7044-4350
Padmapriyadarshini RavisankarDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0002-7061-9875
Fouley T TireraDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.
Kendall E MartinDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0002-6563-9855
Jacob T GafranekDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0002-6880-9872
Tiffany B DuongDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0001-8923-1881
Terri L VanDykeDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0003-3490-1176
Melissa TouvronDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0003-1229-5152
Lindsey A BarskeEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, University of Southern California, Los Angeles, CA, United States of America.ORCID 0000-0003-1275-7978
J Gage CrumpEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, University of Southern California, Los Angeles, CA, United States of America.
Joshua S WaxmanDivision of Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States of America.ORCID 0000-0002-8132-487X
Cincinnati Children's Hospital Medical Center · USUniversity of Southern California · US

Funding

Progenitor Regulation in Craniofacial Development and RegenerationR35DE027550 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CRUMP, GAGE D · 2017 to 2024
$8.0M
TRAINING IN CARDIOVASCULAR BIOLOGYT32HL007382 · NHLBI · UNIVERSITY OF CINCINNATI · PI SCHWARTZ, ARNOLD · 1985 to 2012
$5.9M
Epithelial-mesenchymal interactions in facial patterningR01DE018405 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CRUMP, GAGE D · 2007 to 2017
$4.1M
Molecular Mechanisms of Atrial Development and RegenerationR01HL137766 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Joshua Waxman · 2017 to 2026
$3.9M
Coup-tf dependent mechanisms of ventricular and hemangioblast specificationR01HL112893 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI WAXMAN, JOSHUA · 2013 to 2017
$1.7M
Prolonged Progenitor Maintenance Sculpts the Upper FaceK99DE026239 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BARSKE, LINDSEY ANNE · 2016 to 2017
$252k
NHLBI NIH HHS R01 HL112893NHLBI NIH HHS R01 HL137766NHLBI NIH HHS T32 HL007382NIDCR NIH HHS K99 DE026239NIDCR NIH HHS R01 DE018405NIDCR NIH HHS R35 DE027550
6 · The paper itself

Abstract

Multiple syndromes share congenital heart and craniofacial muscle defects, indicating there is an intimate relationship between the adjacent cardiac and pharyngeal muscle (PM) progenitor fields. However, mechanisms that direct antagonistic lineage decisions of the cardiac and PM progenitors within the anterior mesoderm of vertebrates are not understood. Here, we identify that retinoic acid (RA) signaling directly promotes the expression of the transcription factor Nr2f1a within the anterior lateral plate mesoderm. Using zebrafish nr2f1a and nr2f2 mutants, we find that Nr2f1a and Nr2f2 have redundant requirements restricting ventricular cardiomyocyte (CM) number and promoting development of the posterior PMs. Cre-mediated genetic lineage tracing in nr2f1a; nr2f2 double mutants reveals that tcf21+ progenitor cells, which can give rise to ventricular CMs and PM, more frequently become ventricular CMs potentially at the expense of posterior PMs in nr2f1a; nr2f2 mutants. Our studies reveal insights into the molecular etiology that may underlie developmental syndromes that share heart, neck and facial defects as well as the phenotypic variability of congenital heart defects associated with NR2F mutations in humans.

Indexed as

AnimalsAnimals, Genetically ModifiedBody PatterningCell LineageCOUP Transcription Factor IICraniofacial AbnormalitiesDNA-Binding ProteinsEmbryonic Stem CellsHeart Defects, CongenitalHeart VentriclesHumansMesodermModels, AnimalMutationMyocytes, CardiacPharyngeal MusclesCOUP Transcription Factor IIDNA-Binding Proteinsnr2f1a protein, zebrafishTranscription FactorsTretinoinZebrafish Proteins

Identifiers

PMID30721228
PMCPMC6377147
OpenAlexW2912036099

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.