Evidence map›Paper›PMID 34597846›Full record

ArticleCells & development2021

The zebrafish presomitic mesoderm elongates through compaction-extension.

Lewis Thomson, Leila Muresan, Benjamin Steventon

Abstract read
In one paragraph

Article in Cells & development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Evolvability in vertebrate segmentation.Seminars in cell & developmental biology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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  11. Science advances · 2024
    Article
  12. Review
  13. Article
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  15. Article
  16. Review
  17. Review
  18. In preprints: the problem of producing precise patterns.Development (Cambridge, England) · 2022
    Article
  19. 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

3 authors.

Lewis ThomsonDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, UK.
Leila MuresanCambridge Advanced Imaging Centre, University of Cambridge, Cambridge, UK.
Benjamin SteventonDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, UK. Electronic address: bjs57@cam.ac.uk.

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust 109408
6 · The paper itself

Abstract

In vertebrate embryos the presomitic mesoderm becomes progressively segmented into somites at the anterior end while extending along the anterior-posterior axis. A commonly adopted model to explain how this tissue elongates is that of posterior growth, driven in part by the addition of new cells from uncommitted progenitor populations in the tailbud. However, in zebrafish, much of somitogenesis is associated with an absence of overall volume increase, and posterior progenitors do not contribute new cells until the final stages of somitogenesis. Here, we perform a comprehensive 3D morphometric analysis of the paraxial mesoderm and reveal that extension is linked to a volumetric decrease and an increase in cell density. We also find that individual cells decrease in volume over successive somite stages. Live cell tracking confirms that much of this tissue deformation occurs within the presomitic mesoderm progenitor zone and is associated with non-directional rearrangement. Taken together, we propose a compaction-extension mechanism of tissue elongation that highlights the need to better understand the role tissue intrinsic and extrinsic forces in regulating morphogenesis.

Indexed as

MesodermZebrafishAnimalsEmbryonic DevelopmentMorphogenesisSomitesDevelopmental morphometricsMorphogenesisMulti-tissuePosterior bodySomitogenesis

Identifiers

PMID34597846
PMCPMC7612712

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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.