Evidence map›Paper›PMID 29877796›Full record

ArticleeLife2018

BMP and FGF signaling interact to pattern mesoderm by controlling basic helix-loop-helix transcription factor activity.

Richard H Row, Amy Pegg, Brian A Kinney, Gist H Farr, Lisa Maves, Sally Lowell, Valerie Wilson, Benjamin L Martin

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-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

26 citing papers in PubMed, 53 citations in OpenAlex.

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  14. iScience · 2023
    Article
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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 3 institutions in 2 countries.

Richard H Row *Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, United States.
Amy Pegg *MRC Center for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Brian A KinneyDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, United States.
Gist H FarrCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, United States.
Lisa MavesCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, United States.
Sally LowellMRC Center for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.ORCID http://orcid.org/0000-0002-4018-9480
Valerie WilsonMRC Center for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.ORCID http://orcid.org/0000-0003-4182-5159
Benjamin L MartinDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, United States.ORCID http://orcid.org/0000-0001-5474-4492
Seattle Children's Hospital · USMRC Centre for Regenerative Medicine · GBStony Brook University · US

Funding

Regulation of muscle fiber type and resistance to muscular dystrophyR03AR065760 · NIAMS · SEATTLE CHILDREN'S HOSPITAL · PI MAVES, LISA · 2014 to 2016
$293k
Medical Research Council Mr/K011200/1Medical Research Council MR/K017047/1NIAMS NIH HHS R03 AR065760Wellcome TrustWellcome Trust Senior Fellowship in Basic Biomedical Science 103789/Z/14/Z
6 · The paper itself

Abstract

The mesodermal germ layer is patterned into mediolateral subtypes by signaling factors including BMP and FGF. How these pathways are integrated to induce specific mediolateral cell fates is not well understood. We used mesoderm derived from post-gastrulation neuromesodermal progenitors (NMPs), which undergo a binary mediolateral patterning decision, as a simplified model to understand how FGF acts together with BMP to impart mediolateral fate. Using zebrafish and mouse NMPs, we identify an evolutionarily conserved mechanism of BMP and FGF-mediated mediolateral mesodermal patterning that occurs through modulation of basic helix-loop-helix (bHLH) transcription factor activity. BMP imparts lateral fate through induction of Id helix loop helix (HLH) proteins, which antagonize bHLH transcription factors, induced by FGF signaling, that specify medial fate. We extend our analysis of zebrafish development to show that bHLH activity is responsible for the mediolateral patterning of the entire mesodermal germ layer.

Indexed as

Signal TransductionAnimalsAnimals, Genetically ModifiedBasic Helix-Loop-Helix ProteinsBody PatterningBone Morphogenetic ProteinsCell DifferentiationCells, CulturedEmbryo, NonmammalianFibroblast Growth FactorsGene Expression Regulation, DevelopmentalMesodermMiceZebrafishZebrafish ProteinsBasic Helix-Loop-Helix ProteinsBone Morphogenetic ProteinsFibroblast Growth FactorsZebrafish ProteinsbHLHBMPdevelopmental biologyFGFmesodermmorphogenmouseneuromesodermal progenitorregenerative medicinestem cellszebrafish

Identifiers

PMID29877796
PMCPMC6013256
OpenAlexW2806393368

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.