Evidence map›Paper›PMID 22135404›Full record

ArticleCirculation research2012

Etsrp/Etv2 is directly regulated by Foxc1a/b in the zebrafish angioblast.

Matthew B Veldman, Shuo Lin

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 62 citations in OpenAlex.

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  12. Zebrafish etv2 knock-in line labels vascular endothelial and blood progenitor cells.Developmental dynamics : an official publication of the American Association of Anatomists · 2020
    Article
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  14. ETV2/ER71 regulates the generation of FLK1Stem cell research & therapy · 2019
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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

2 authors at 1 institution in 1 country.

Matthew B VeldmanDepartment of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, 621 Charles E Young Dr South, Los Angeles, CA 90095-1606, USA.
Shuo Lin
University of California, Los Angeles · US

Funding

Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
GENETIC ANALYSIS OF HEMATOPOIETIC DEVELOPMENTR01DK054508 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LIN, SHUO · 1998 to 2012
$3.4M
NHLBI NIH HHS T32 HL069766NHLBI NIH HHS T32 HL08634NHLBI NIH HHS T32HL69766NIDDK NIH HHS 5R01DK054508-13NIDDK NIH HHS R01 DK054508
6 · The paper itself

Abstract

rationaleEndothelial cells are developmentally derived from angioblasts specified in the mesodermal germ cell layer. The transcription factor etsrp/etv2 is at the top of the known genetic hierarchy for angioblast development. The transcriptional events that induce etsrp expression and angioblast specification are not well understood.

objectiveWe generated etsrp:gfp transgenic zebrafish and used them to identify regulatory regions and transcription factors critical for etsrp expression and angioblast specification from mesoderm. METHODS AND

resultsTo investigate the mechanisms that initiate angioblast cell transcription during embryogenesis, we have performed promoter analysis of the etsrp locus in zebrafish. We describe three enhancer elements sufficient for endothelial gene expression when place in front of a heterologous promoter. The deletion of all 3 regulatory regions led to a near complete loss of endothelial expression from the etsrp promoter. One of the enhancers, located 2.3 kb upstream of etsrp contains a consensus FOX binding site that binds Foxc1a and Foxc1b in vitro by EMSA and in vivo using ChIP. Combined knockdown of foxc1a/b, using morpholinos, led to a significant decrease in etsrp expression at early developmental stages as measured by quantitative reverse transcriptase-polymerase chain reaction and in situ hybridization. Decreased expression of primitive erythrocyte genes scl and gata1 was also observed, whereas pronephric gene pax2a was relatively normal in expression level and pattern.

conclusionsThese findings identify mesodermal foxc1a/b as a direct upstream regulator of etsrp in angioblasts. This establishes a new molecular link in the process of mesoderm specification into angioblast.

Indexed as

Cell LineageAnimalsAnimals, Genetically ModifiedBase SequenceBinding SitesChromatin ImmunoprecipitationElectrophoretic Mobility Shift AssayEmbryonic Stem CellsEmbryo, NonmammalianEndothelial CellsForkhead Transcription FactorsGene Expression Regulation, DevelopmentalGene Knockdown TechniquesIn Situ HybridizationMesodermMicroscopy, FluorescenceEtv2 protein, zebrafishForkhead Transcription FactorsFoxc1a protein, zebrafishFoxc1b protein, zebrafishRecombinant Fusion ProteinsZebrafish Proteins

Identifiers

PMID22135404
PMCPMC3457812
OpenAlexW2171040147

What OpenQuestion holds

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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.