Evidence map›Paper›PMID 21098565›Full record

ArticleDevelopment (Cambridge, England)2010

Initiation of trophectoderm lineage specification in mouse embryos is independent of Cdx2.

Guangming Wu, Luca Gentile, Takuya Fuchikami, Julien Sutter, Katherina Psathaki, Telma C Esteves, Marcos J Araúzo-Bravo, Claudia Ortmeier, Gaby Verberk, Kuniya Abe and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.6field-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

60 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. GDF-8 improvesFrontiers in cell and developmental biology · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Journey of the mouse primitive endoderm: from specification to maturation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  12. International journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Nested information processing in the living world.Annals of the New York Academy of Sciences · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

11 authors at 2 institutions in 1 country.

Guangming WuDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149 Münster, Germany.
Luca Gentile
Takuya Fuchikami
Julien Sutter
Katherina Psathaki
Telma C Esteves
Marcos J Araúzo-Bravo
Claudia Ortmeier
Gaby Verberk
Kuniya Abe
Hans R Schöler
Max Planck Institute for Molecular Biomedicine · DEUniversity of Münster · DE

Funding

Altered Nuclear TransferR01HD059946 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI MITALIPOV, SHOUKHRAT · 2010 to 2014
$2.7M
NICHD NIH HHS R01 HD059946NICHD NIH HHS R01HD059946-01
6 · The paper itself

Abstract

The separation of the first two lineages - trophectoderm (TE) and inner cell mass (ICM) - is a crucial event in the development of the early embryo. The ICM, which constitutes the pluripotent founder cell population, develops into the embryo proper, whereas the TE, which comprises the surrounding outer layer, supports the development of the ICM before and after implantation. Cdx2, the first transcription factor expressed specifically in the developing TE, is crucial for the differentiation of cells into the TE, as lack of zygotic Cdx2 expression leads to a failure of embryos to hatch and implant into the uterus. However, speculation exists as to whether maternal Cdx2 is required for initiation of TE lineage separation. Here, we show that effective elimination of both maternal and zygotic Cdx2 transcripts by an RNA interference approach resulted in failure of embryo hatching and implantation, but the developing blastocysts exhibited normal gross morphology, indicating that TE differentiation had been initiated. Expression of keratin 8, a marker for differentiated TE, further confirmed the identity of the TE lineage in Cdx2-deficient embryos. However, these embryos exhibited low mitochondrial activity and abnormal ultrastructure, indicating that Cdx2 plays a key role in the regulation of TE function. Furthermore, we found that embryonic compaction does not act as a 'switch' regulator to turn on Cdx2 expression. Our results clearly demonstrate that neither maternal nor zygotic Cdx2 transcripts direct the initiation of ICM/TE lineage separation.

Indexed as

Adenosine TriphosphateAnimalsCDX2 Transcription FactorCell ProliferationDNA-Binding ProteinsEmbryo, MammalianFemaleHomeodomain ProteinsImmunohistochemistryIn Situ Nick-End LabelingMaleMembrane Potential, MitochondrialMiceMicroscopy, Electron, TransmissionMuscle ProteinsOocytesAdenosine TriphosphateCdx2 protein, mouseCDX2 Transcription FactorDNA-Binding ProteinsHomeodomain ProteinsMuscle ProteinsTead4 protein, mouseTEA Domain Transcription FactorsTranscription Factors

Identifiers

PMID21098565
PMCPMC2990207
OpenAlexW2130273514

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.