Evidence map›Paper›PMID 19269286›Full record

ArticleDevelopmental biology2009

A genetic screen for vascular mutants in zebrafish reveals dynamic roles for Vegf/Plcg1 signaling during artery development.

L D Covassin, A F Siekmann, M C Kacergis, E Laver, J C Moore, J A Villefranc, B M Weinstein, N D Lawson

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

79 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
  2. Article
  3. Single-Cell-Resolution Fate Mapping Reveals Embryonic Venous Origins of Fenestrated Hindbrain Choroid Plexus Vasculature.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Endothelial cell transitions in zebrafish vascular development.Development, growth & differentiation · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Journal of vascular anomalies · 2023
    Article
  13. Article
  14. Detecting Förster resonance energy transfer in living cells by conventional and spectral flow cytometry.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

19 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 2 institutions in 2 countries.

L D CovassinProgram in Gene Function and Expression, University of Massachusetts Medical School, Lazare Research Building, Room 617, 364 Plantation Street, Worcester, MA 01605, USA.
A F Siekmann
M C Kacergis
E Laver
J C Moore
J A Villefranc
B M Weinstein
N D Lawson
University of Massachusetts Chan Medical School · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Specification And Patterning of Developing Blood VesselsZIAHD001011 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI WEINSTEIN, BRANT · 2009 to 2025
$18.4M
Role of Plcg1 in Vegf signalingR01CA107454 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LAWSON, NATHAN D · 2005 to 2009
$1.5M
Plcg1 integration of Vegf receptor signalingF31HL081927 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI VILLEFRANC, JACQUES ALPHONSE · 2005 to 2008
$86k
NCI NIH HHS R01 CA107454NCI NIH HHS R01CA107454NHLBI NIH HHS F31 HL081927NHLBI NIH HHS F31HL081927
6 · The paper itself

Abstract

In this work we describe a forward genetic approach to identify mutations that affect blood vessel development in the zebrafish. By applying a haploid screening strategy in a transgenic background that allows direct visualization of blood vessels, it was possible to identify several classes of mutant vascular phenotypes. Subsequent characterization of mutant lines revealed that defects in Vascular endothelial growth factor (Vegf) signaling specifically affected artery development. Comparison of phenotypes associated with different mutations within a functional zebrafish Vegf receptor-2 ortholog (referred to as kdr-like, kdrl) revealed surprisingly varied effects on vascular development. In parallel, we identified an allelic series of mutations in phospholipase c gamma 1 (plcg1). Together with in vivo structure-function analysis, our results suggest a requirement for Plcg1 catalytic activity downstream of receptor tyrosine kinases. We further find that embryos lacking both maternal and zygotic plcg1 display more severe defects in artery differentiation but are otherwise similar to zygotic mutants. Finally, we demonstrate through mosaic analysis that plcg1 functions autonomously in endothelial cells. Together our genetic analyses suggest that Vegf/Plcg1 signaling acts at multiple time points and in different signaling contexts to mediate distinct aspects of artery development.

Indexed as

MutationSignal TransductionAmino Acid SequenceAnimalsAnimals, Genetically ModifiedArteriesBase SequenceDNA PrimersFemaleMaleMolecular Sequence DataMosaicismPhospholipase C gammaSequence Homology, Amino AcidVascular Endothelial Growth Factor AZebrafishDNA PrimersPhospholipase C gammaVascular Endothelial Growth Factor A

Identifiers

PMID19269286
PMCPMC2791107
OpenAlexW1983929532

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.