Evidence map›Paper›PMID 34528691›Full record

ArticleDevelopment (Cambridge, England)2021

YAP establishes epiblast responsiveness to inductive signals for germ cell fate.

Saya Kagiwada, Shinya Aramaki, Guangming Wu, Borami Shin, Eva Kutejova, David Obridge, Kenjiro Adachi, Jeffrey L Wrana, Karin Hübner, Hans R Schöler

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. The many dimensions of germline competence.Current opinion in cell biology · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
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

10 authors at 4 institutions in 3 countries.

Saya KagiwadaDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Shinya AramakiDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Guangming WuDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Borami ShinDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Eva KutejovaDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
David ObridgeDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Kenjiro AdachiDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Jeffrey L WranaDepartment of Cancer Biology, Centre for Systems Biology, Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada.
Karin HübnerDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.
Hans R SchölerDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster 48149, Germany.ORCID 0000-0003-2643-5136
Max Planck Institute for Molecular Biomedicine · DEGuangzhou Regenerative Medicine and Health Guangdong Laboratory · CNMount Sinai Hospital · CAUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The germ cell lineage in mammals is induced by the stimulation of pluripotent epiblast cells by signaling molecules. Previous studies have suggested that the germ cell differentiation competence or responsiveness of epiblast cells to signaling molecules is established and maintained in epiblast cells of a specific differentiation state. However, the molecular mechanism underlying this process has not been well defined. Here, using the differentiation model of mouse epiblast stem cells (EpiSCs), we have shown that two defined EpiSC lines have robust germ cell differentiation competence. However, another defined EpiSC line has no competence. By evaluating the molecular basis of EpiSCs with distinct germ cell differentiation competence, we identified YAP, an intracellular mediator of the Hippo signaling pathway, as crucial for the establishment of germ cell induction. Strikingly, deletion of YAP severely affected responsiveness to inductive stimuli, leading to a defect in WNT target activation and germ cell differentiation. In conclusion, we propose that the Hippo/YAP signaling pathway creates a potential for germ cell fate induction via mesodermal WNT signaling in pluripotent epiblast cells.

Indexed as

AnimalsCell DifferentiationCell LineageFemaleGerm CellsGerm LayersHippo Signaling PathwayMaleMiceStem CellsWnt Signaling PathwayYAP-Signaling ProteinsYap1 protein, mouseYAP-Signaling ProteinsEpiSCsHippo pathwayMousePGCsPluripotent stem cells

Identifiers

PMID34528691
PMCPMC8571999
OpenAlexW3200856768

What OpenQuestion holds

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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.