Evidence map›Paper›PMID 17662710›Full record

ArticleDevelopmental biology2007

The anterior visceral endoderm of the mouse embryo is established from both preimplantation precursor cells and by de novo gene expression after implantation.

Maria-Elena Torres-Padilla, Lucy Richardson, Paulina Kolasinska, Sigolène M Meilhac, Merlin Verena Luetke-Eversloh, Magdalena Zernicka-Goetz

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Vertebrate Axial Patterning: From Egg to Asymmetry.Advances in experimental medicine and biology · 2017
    Review
  9. Review
  10. Article
  11. Activin/Nodal signalling before implantation: setting the stage for embryo patterning.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  12. Heading forwards: anterior visceral endoderm migration in patterning the mouse embryo.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  13. Review
  14. Article
  15. The hypoblast (visceral endoderm): an evo-devo perspective.Development (Cambridge, England) · 2012
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Maria-Elena Torres-PadillaThe Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Lucy Richardson
Paulina Kolasinska
Sigolène M Meilhac
Merlin Verena Luetke-Eversloh
Magdalena Zernicka-Goetz
University of Cambridge · GB

Funding

Medical Research Council G0300723Medical Research Council G0800784Wellcome Trust 064421
6 · The paper itself

Abstract

Initiation of the development of the anterior-posterior axis in the mouse embryo has been thought to take place only when the anterior visceral endoderm (AVE) emerges and starts its asymmetric migration. However, expression of Lefty1, a marker of the AVE, was recently found to initiate before embryo implantation. This finding has raised two important questions: are the cells that show such early, preimplantation expression of this AVE marker the real precursors of the AVE and, if so, how does this contribute to the establishment of the AVE? Here, we address both of these questions. First, we show that the expression of another AVE marker, Cer1, also commences before implantation and its expression becomes consolidated in the subset of ICM cells that comprise the primitive endoderm. Second, to determine whether the cells showing this early Cer1 expression are true precursors of the AVE, we set up conditions to trace these cells in time-lapse studies from early periimplantation stages until the AVE emerges and becomes asymmetrically displaced. We found that Cer1-expressing cells are asymmetrically located after implantation and, as the embryo grows, they become dispersed into two or three clusters. The expression of Cer1 in the proximal domain is progressively diminished, whilst it is reinforced in the distal-lateral domain. Our time-lapse studies demonstrate that this distal-lateral domain is incorporated into the AVE together with cells in which Cer1 expression begins only after implantation. Thus, the AVE is formed from both part of an ancestral population of Cerl-expressing cells and cells that acquire Cer1 expression later. Finally, we demonstrate that when the AVE shifts asymmetrically to establish the anterior pole, this occurs towards the region where the earlier postimplantation expression of Cer1 was strongest. Together, these results suggest that the orientation of the anterior-posterior axis is already anticipated before AVE migration.

Indexed as

Embryo ImplantationAnimalsAntigens, DifferentiationBody PatterningCell DifferentiationCell MovementCytokinesEmbryonic Stem CellsEndodermMiceProteinsAntigens, DifferentiationCer1 protein, mouseCytokinesProteins

Identifiers

PMID17662710
PMCPMC3353121
OpenAlexW1974368058

What OpenQuestion holds

Textmetadata
LicenceTDM
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.