Evidence map›Paper›PMID 25512302›Full record

ArticleDevelopmental biology2015

Maternal-zygotic knockout reveals a critical role of Cdx2 in the morula to blastocyst transition.

Agnieszka Jedrusik, Andy Cox, Krzysztof B Wicher, David M Glover, Magdalena Zernicka-Goetz

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-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

23 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  11. Maternal factors regulating preimplantation development in mice.Current topics in developmental biology · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Single-cell gene expression of the bovine blastocyst.Reproduction (Cambridge, England) · 2017
    Article
  17. Article
  18. Causes and evolutionary consequences of primordial germ-cell specification mode in metazoans.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Article
  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

5 authors at 1 institution in 1 country.

Agnieszka JedrusikDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Site, Cambridge CB2 3DY, UK.
Andy CoxDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Site, Cambridge CB2 3DY, UK.
Krzysztof B WicherDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Site, Cambridge CB2 3DY, UK.
David M GloverDepartment of Genetics, University of Cambridge, Downing Site, Cambridge CB2 3EH, UK.
Magdalena Zernicka-GoetzDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Site, Cambridge CB2 3DY, UK.
University of Cambridge · GB

Funding

Cancer Research UK 11431Medical Research Council G1001696Wellcome Trust 098287/Z/12/Z
6 · The paper itself

Abstract

The first lineage segregation in the mouse embryo generates the inner cell mass (ICM), which gives rise to the pluripotent epiblast and therefore the future embryo, and the trophectoderm (TE), which will build the placenta. The TE lineage depends on the transcription factor Cdx2. However, when Cdx2 first starts to act remains unclear. Embryos with zygotic deletion of Cdx2 develop normally until the late blastocyst stage leading to the conclusion that Cdx2 is important for the maintenance but not specification of the TE. In contrast, down-regulation of Cdx2 transcripts from the early embryo stage results in defects in TE specification before the blastocyst stage. Here, to unambiguously address at which developmental stage Cdx2 becomes first required, we genetically deleted Cdx2 from the oocyte stage using a Zp3-Cre/loxP strategy. Careful assessment of a large cohort of Cdx2 maternal-zygotic null embryos, all individually filmed, examined and genotyped, reveals an earlier lethal phenotype than observed in Cdx2 zygotic null embryos that develop until the late blastocyst stage. The developmental failure of Cdx2 maternal-zygotic null embryos is associated with cell death and failure of TE specification, starting at the morula stage. These results indicate that Cdx2 is important for the correct specification of TE from the morula stage onwards and that both maternal and zygotic pools of Cdx2 are required for correct pre-implantation embryogenesis.

Indexed as

Gene Knockout TechniquesAnimalsBlastocystBody PatterningBreedingCDX2 Transcription FactorCell DeathEctodermEmbryonic DevelopmentFemaleHomeodomain ProteinsMaleMiceMorulaTranscription FactorsZygoteCdx2 protein, mouseCDX2 Transcription FactorHomeodomain ProteinsTranscription FactorsCdx2Maternal-zygotic knockoutMouse embryoTrophectoderm

Identifiers

PMID25512302
PMCPMC4319684
OpenAlexW1991711696

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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.