Evidence map›Paper›PMID 28935706›Full record

ArticleDevelopment (Cambridge, England)2017

Suppression of ERK signalling abolishes primitive endoderm formation but does not promote pluripotency in rabbit embryo.

Anna Piliszek, Zofia E Madeja, Berenika Plusa

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

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  6. Alternative mammalian strategies leading towards gastrulation: losing polar trophoblast (Rauber's layer) or gaining an epiblast cavity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  7. Journey of the mouse primitive endoderm: from specification to maturation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
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  20. OCT4/POU5F1 is required for NANOG expression in bovine blastocysts.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

3 authors at 3 institutions in 2 countries.

Anna PiliszekDepartment of Experimental Embryology, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Postępu 36a, 05-552 Jastrzębiec, Poland a.piliszek@ighz.pl berenika.plusa@manchester.ac.uk.ORCID 0000-0003-1449-3523
Zofia E MadejaDepartment of Genetics and Animal Breeding, Faculty of Veterinary Medicine and Animal Sciences, Poznan University of Life Sciences, Wołyńska 33, 60-637 Poznań, Poland.ORCID 0000-0001-9649-2422
Berenika PlusaFaculty of Biology, Medicine and Health, The University of Manchester, Oxford Road, Manchester M13 9PT, UK a.piliszek@ighz.pl berenika.plusa@manchester.ac.uk.ORCID 0000-0003-2214-5940
Polish Academy of Sciences · PLUniversity of Life Sciences in Poznań · PLUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formation of epiblast (EPI) - the founder line of all embryonic lineages - and extra-embryonic supportive tissues is one of the key events in mammalian development. The prevailing model of early mammalian development is based almost exclusively on the mouse. Here, we provide a comprehensive, stage-by-stage analysis of EPI and extra-embryonic primitive endoderm (PrE) formation during preimplantation development of the rabbit. Although we observed that rabbit embryos have several features in common with mouse embryos, including a stage-related initiation of lineage specification, our results demonstrate the existence of some key differences in lineage specification among mammals. Contrary to the current view, our data suggest that reciprocal repression of GATA6 and NANOG is not fundamental for the initial stages of PrE versus EPI specification in mammals. Furthermore, our results provide insight into the observed discrepancies relating to the role of FGF/ERK signalling in PrE versus EPI specification between mouse and other mammals.

Indexed as

Gene Expression Regulation, DevelopmentalMAP Kinase Signaling SystemAnimalsBlastocystCell DifferentiationCell LineageEndodermExtracellular Signal-Regulated MAP KinasesFemaleGATA6 Transcription FactorGene Expression ProfilingGerm LayersHMGB ProteinsMiceNanog Homeobox ProteinRabbitsExtracellular Signal-Regulated MAP KinasesGata6 protein, mouseGATA6 Transcription FactorHMGB ProteinsNanog Homeobox ProteinSox17 protein, mouseSox2 protein, mouseSOXB1 Transcription FactorsSOXF Transcription FactorsBlastocystEpiblastFGFPrimitive endodermRabbit

Identifiers

PMID28935706
PMCPMC5675450
OpenAlexW2756678656

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.