Evidence map›Paper›PMID 28818668›Full record

ArticleDevelopmental biology2017

A bipolar role of the transcription factor ERG for cnidarian germ layer formation and apical domain patterning.

Aldine R Amiel, Hereroa Johnston, Taylor Chock, Paul Dahlin, Marta Iglesias, Michael Layden, Eric Röttinger, Mark Q Martindale

Abstract read
In one paragraph

Article in Developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 36 citations in OpenAlex.

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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 5 institutions in 4 countries.

Aldine R AmielUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice, France.
Hereroa JohnstonUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice, France.
Taylor ChockUniversity of Florida, The Whitney Marine Laboratory for Marine Science, St. Augustine, FL, USA.
Paul DahlinStockholm University, Department of Ecology, Environment and Plant Sciences, Stockholm, Sweden.
Marta IglesiasUniversity of Barcelona, Department of Genetics and Institute of Biomedicine, Barcelona, Spain.
Michael LaydenLehigh University, Department of Biological Sciences, Bethlehem, PA, USA.
Eric RöttingerUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging, Nice, France. Electronic address: eric.rottinger@unice.fr.
Mark Q MartindaleUniversity of Florida, The Whitney Marine Laboratory for Marine Science, St. Augustine, FL, USA. Electronic address: mqmartin@whitney.ufl.edu.
Centre National de la Recherche Scientifique · FRMote Marine Laboratory · USInstitute for Research in Biomedicine · ESLehigh University · USStockholm University · SE

Funding

Gene regulatory network evolution and the origin of biological noveltiesR01GM093116 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI MARTINDALE, MARK Q · 2010 to 2013
$1.1M
NIGMS NIH HHS R01 GM093116
6 · The paper itself

Abstract

Germ layer formation and axial patterning are biological processes that are tightly linked during embryonic development of most metazoans. In addition to canonical WNT, it has been proposed that ERK-MAPK signaling is involved in specifying oral as well as aboral territories in cnidarians. However, the effector and the molecular mechanism underlying latter phenomenon is unknown. By screening for potential effectors of ERK-MAPK signaling in both domains, we identified a member of the ETS family of transcription factors, Nverg that is bi-polarily expressed prior to gastrulation. We further describe the crucial role of NvERG for gastrulation, endomesoderm as well as apical domain formation. The molecular characterization of the obtained NvERG knock-down phenotype using previously described as well as novel potential downstream targets, provides evidence that a single transcription factor, NvERG, simultaneously controls expression of two different sets of downstream targets, leading to two different embryonic gene regulatory networks (GRNs) in opposite poles of the developing embryo. We also highlight the molecular interaction of cWNT and MEK/ERK/ERG signaling that provides novel insight into the embryonic axial organization of Nematostella, and show a cWNT repressive role of MEK/ERK/ERG signaling in segregating the endomesoderm in two sub-domains, while a common input of both pathways is required for proper apical domain formation. Taking together, we build the first blueprint for a global cnidarian embryonic GRN that is the foundation for additional gene specific studies addressing the evolution of embryonic and larval development.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBody PatterningDNA, ComplementaryEmbryo, NonmammalianFibroblast Growth FactorsGastrulationGene Knockdown TechniquesGene Regulatory NetworksGerm LayersMAP Kinase Signaling SystemMesodermSea AnemonesTranscription FactorsWnt Signaling PathwayDNA, ComplementaryFibroblast Growth FactorsTranscription FactorsApical organCnidarianEmbryonic developmentEndomesodermERGERK signalingETS transcription factorEvolutionGastrulationGene expressionGene regulatory networkNematostella vectensisSea anemone

Identifiers

PMID28818668
PMCPMC5623658
OpenAlexW2750368203

What OpenQuestion holds

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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.