Evidence map›Paper›PMID 19164561›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

FGF-dependent left-right asymmetry patterning in zebrafish is mediated by Ier2 and Fibp1.

Sung-Kook Hong, Igor B Dawid

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
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  5. Review
  6. Origin, form and function of extraembryonic structures in teleost fishes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  7. Review
  8. Frontiers in cell and developmental biology · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. The primary cilium as a signaling nexus for growth plate function and subsequent skeletal development.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Kupffer's vesicle size threshold for robust left-right patterning of the zebrafish embryo.Developmental dynamics : an official publication of the American Association of Anatomists · 2016
    Article
  20. Article
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.

Sung-Kook HongLaboratory of Molecular Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Igor B Dawid
National Institutes of Health · US

Funding

Developmental Genetics in the Zebrafish Danio rerioZIAHD008809 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI DAWID, IGOR B · 2009 to 2016
$7.8M
Gene Expression During Embryonic Development Of Xenopus LaevisZIAHD001002 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI DAWID, IGOR B · 2009 to 2016
$3.0M
Developmental Genetics in the Zebrafish Danio rerioZ01HD008809 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI DAWID, IGOR B · 2007 to 2008
$2.4M
Intramural NIH HHS
6 · The paper itself

Abstract

Establishment of left-right asymmetry in vertebrates requires nodal, Wnt-PCP and FGF signaling and involves ciliogenesis in a laterality organ. Effector genes through which FGF signaling affects laterality have not been described. We isolated the zebrafish ier2 and fibp1 genes as FGF target genes and show that their protein products interact. Knock down of these factors interferes with establishment of organ laterality and causes defective cilia formation in Kupffer's Vesicle, the zebrafish laterality organ. Cilia are also lost after suppression of FGF8, but can be rescued by injection of ier2 and fibp1 mRNA. We conclude that Ier2 and Fibp1 mediate FGF signaling in ciliogenesis in Kupffer's Vesicle and in the establishment of laterality in the zebrafish embryo.

Indexed as

Body PatterningGene Expression Regulation, DevelopmentalAnimalsCarrier ProteinsCell LineDevelopmental BiologyFibroblast Growth FactorsHumansImmediate-Early ProteinsIn Situ HybridizationModels, BiologicalPhenotypeRNA, MessengerTwo-Hybrid System TechniquesZebrafishZebrafish ProteinsCarrier Proteinsfgf8a protein, zebrafishfibpa protein, zebrafishFibroblast Growth Factorsier2a protein, zebrafishImmediate-Early ProteinsRNA, MessengerZebrafish Proteins

Identifiers

PMID19164561
PMCPMC2650137
OpenAlexW2065132553

What OpenQuestion holds

Textmetadata
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.