Evidence map›Paper›PMID 22142964›Full record

ArticleDevelopmental biology2012

Differential regulation of epiboly initiation and progression by zebrafish Eomesodermin A.

Susan Du, Bruce W Draper, Marina Mione, Cecilia B Moens, Ashley Bruce

Abstract read
In one paragraph

Article in Developmental biology, 2012. 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 20% 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, 46 citations in OpenAlex.

  1. Early ultraviolet exposure disrupts late dorsal fin skeletal development in zebrafish.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  2. CRISPR/Cas9-Mediated Disruption ofInternational journal of molecular sciences · 2025
    Article
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  7. Maternal Factors and Nodal Autoregulation OrchestrateFrontiers in cell and developmental biology · 2022
    Article
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  9. Frontiers in cell and developmental biology · 2021
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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

5 authors at 4 institutions in 3 countries.

Susan DuDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
Bruce W Draper
Marina Mione
Cecilia B Moens
Ashley Bruce
University of Toronto · CAHoward Hughes Medical Institute · USIFOM · ITUniversity of California, Davis · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
TILLING the Zebrafish Genome: A Reverse Genetic ApproachR01HG002995 · NHGRI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, POSTLETHWAIT, JOHN H. · 2003 to 2010
$3.5M
TILLING the Zebrafish Genome: A Reverse Genetics ApproachR01HD076585 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, SOLNICAKREZEL, LILIANNA · 2012 to 2014
$1.9M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA015704NHGRI NIH HHS HG002995NHGRI NIH HHS R01 HG002995NICHD NIH HHS R01 HD076585
6 · The paper itself

Abstract

The T-box transcription factor Eomesodermin (Eomes) has been implicated in patterning and morphogenesis in frog, fish and mouse. In zebrafish, one of the two Eomes homologs, Eomesa, has been implicated in dorsal-ventral patterning, epiboly and endoderm specification in experiments employing over-expression, dominant-negative constructs and antisense morpholino oligonucleotides. Here we report for the first time the identification and characterization of an Eomesa mutant generated by TILLING. We find that Eomesa has a strictly maternal role in the initiation of epiboly, which involves doming of the yolk cell up into the overlying blastoderm. By contrast, epiboly progression is normal, demonstrating for the first time that epiboly initiation is genetically separable from progression. The yolk cell microtubules, which are required for epiboly, are defective in maternal-zygotic eomesa mutant embryos. In addition, the deep cells of the blastoderm are more tightly packed and exhibit more bleb-like protrusions than cells in control embryos. We postulate that the doming delay may be the consequence both of overly stabilized yolk cell microtubules and defects in the adhesive properties or motility of deep cells. We also show that Eomesa is required for normal expression of the endoderm markers sox32, bon and og9x; however it is not essential for endoderm formation.

Indexed as

AnimalsBase SequenceBlotting, WesternBody PatterningCell AdhesionCell MovementDNA, ComplementaryGastrulaHomeodomain ProteinsImmunohistochemistryIn Situ HybridizationMicrotubulesMolecular Sequence DataSequence Analysis, DNASOX Transcription FactorsT-Box Domain ProteinsDNA, Complementaryeomesa protein, zebrafishHomeodomain Proteinsmixl1 protein, zebrafishsox32 protein, zebrafishSOX Transcription FactorsT-Box Domain ProteinsTranscription FactorsZebrafish Proteins

Identifiers

PMID22142964
PMCPMC3259739
OpenAlexW1964671479

What OpenQuestion holds

Textmetadata
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.