Evidence map›Paper›PMID 30571656›Full record

ArticleReproduction (Cambridge, England)2019

MED20 is essential for early embryogenesis and regulates NANOG expression.

Wei Cui, Chelsea Marcho, Yongsheng Wang, Rinat Degani, Morgane Golan, Kimberly D Tremblay, Jaime A Rivera-Pérez, Jesse Mager

Open access · bronzeAbstract read
In one paragraph

Article in Reproduction (Cambridge, England), 2019. 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
1.0field-weighted citation impact, top 23% 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, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetically Engineered Mice Unveil In Vivo Roles of the Mediator Complex.International journal of molecular sciences · 2023
    Review
  5. Early embryonic lethality of mice lacking POLD2.Molecular reproduction and development · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
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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 3 institutions in 4 countries.

Wei CuiDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
Chelsea MarchoDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
Yongsheng WangKey Laboratory of Animal Biotechnology of the Ministry of Agriculture, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, PR China.
Rinat DeganiDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
Morgane GolanDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
Kimberly D TremblayDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
Jaime A Rivera-PérezDivision of Genes and Development, Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Jesse MagerDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts, USA.
University of Massachusetts Amherst · USNorth West Agriculture and Forestry University · CNUniversity of Massachusetts Chan Medical School · US

Funding

Streamline assessment of early lethal phenotypes in the mouseR01HD083311 · NICHD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MAGER, JESSE · 2015 to 2024
$6.5M
NICHD NIH HHS R01 HD083311
6 · The paper itself

Abstract

Mediator is an evolutionarily conserved multi-subunit complex, bridging transcriptional activators and repressors to the general RNA polymerase II (Pol II) initiation machinery. Though the Mediator complex is crucial for the transcription of almost all Pol II promoters in eukaryotic organisms, the phenotypes of individual Mediator subunit mutants are each distinct. Here, we report for the first time, the essential role of subunit MED20 in early mammalian embryo development. Although Med20 mutant mouse embryos exhibit normal morphology at E3.5 blastocyst stage, they cannot be recovered at early post-gastrulation stages. Outgrowth assays show that mutant blastocysts cannot hatch from the zona pellucida, indicating impaired blastocyst function. Assessments of cell death and cell lineage specification reveal that apoptosis, inner cell mass, trophectoderm and primitive endoderm markers are normal in mutant blastocysts. However, the epiblast marker NANOG is ectopically expressed in the trophectoderm of Med20 mutants, indicative of defects in trophoblast specification. These results suggest that MED20 specifically, and the Mediator complex in general, are essential for the earliest steps of mammalian development and cell lineage specification.

Indexed as

Embryonic DevelopmentGene Expression Regulation, DevelopmentalAnimalsBlastocystCell LineageEmbryo, MammalianFemaleMaleMediator ComplexMiceMice, Inbred C57BLMice, KnockoutNanog Homeobox ProteinMediator ComplexNanog Homeobox ProteinNanog protein, mouse

Identifiers

PMID30571656
PMCPMC6545164
OpenAlexW2905200397

What OpenQuestion holds

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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.