Evidence map›Paper›PMID 26880542›Full record

ArticleeLife2016

Persistence, period and precision of autonomous cellular oscillators from the zebrafish segmentation clock.

Alexis B Webb, Iván M Lengyel, David J Jörg, Guillaume Valentin, Frank Jülicher, Luis G Morelli, Andrew C Oates

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 129 citations in OpenAlex.

  1. Article
  2. Intrinsic period stability of the cyanobacterial circadian oscillator across in vitro and in vivo conditions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. HES1 oscillations are required for cell cycle reentry in oestrogen receptor-positive breast cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Evolvability in vertebrate segmentation.Seminars in cell & developmental biology · 2025
    Review
  6. Modes of Notch signalling in development and disease.Nature reviews. Molecular cell biology · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Cellular and molecular control of vertebrate somitogenesis.Nature reviews. Molecular cell biology · 2024
    Review
  12. Article
  13. Oscillatory control of embryonic development.Development (Cambridge, England) · 2024
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

7 authors at 3 institutions in 3 countries.

Alexis B WebbMRC-National Institute for Medical Research, London, United Kingdom.
Iván M LengyelDepartamento de Física, FCEyN UBA and IFIBA, CONICET, Buenos Aires, Argentina.
David J JörgMax Planck Institute for the Physics of Complex Systems, Dresden, Germany.
Guillaume ValentinMRC-National Institute for Medical Research, London, United Kingdom.
Frank JülicherMax Planck Institute for the Physics of Complex Systems, Dresden, Germany.ORCID http://orcid.org/0000-0003-4731-9185
Luis G MorelliDepartamento de Física, FCEyN UBA and IFIBA, CONICET, Buenos Aires, Argentina.
Andrew C OatesMRC-National Institute for Medical Research, London, United Kingdom.ORCID http://orcid.org/0000-0002-3015-3978
Max Planck Institute of Molecular Cell Biology and Genetics · DEInstitute of Astronomy and Space Physics · ARMax Planck Institute for the Physics of Complex Systems · DE

Funding

Medical Research Council MC_UP_1202/3
6 · The paper itself

Abstract

In vertebrate development, the sequential and rhythmic segmentation of the body axis is regulated by a "segmentation clock". This clock is comprised of a population of coordinated oscillating cells that together produce rhythmic gene expression patterns in the embryo. Whether individual cells autonomously maintain oscillations, or whether oscillations depend on signals from neighboring cells is unknown. Using a transgenic zebrafish reporter line for the cyclic transcription factor Her1, we recorded single tailbud cells in vitro. We demonstrate that individual cells can behave as autonomous cellular oscillators. We described the observed variability in cell behavior using a theory of generic oscillators with correlated noise. Single cells have longer periods and lower precision than the tissue, highlighting the role of collective processes in the segmentation clock. Our work reveals a population of cells from the zebrafish segmentation clock that behave as self-sustained, autonomous oscillators with distinctive noisy dynamics.

Indexed as

Biological ClocksCell Physiological PhenomenaAnimalsAnimals, Genetically ModifiedArtificial Gene FusionBasic Helix-Loop-Helix ProteinsCells, CulturedGene Expression ProfilingGenes, ReporterZebrafishZebrafish ProteinsBasic Helix-Loop-Helix Proteinsher1 protein, zebrafishZebrafish Proteinsbiological clockcomputational biologydevelopmental biologygene expression noiseoscillatorsomitogenesisstem cellssystems biologytheoretical modellingtimelapse imagingzebrafish

Identifiers

PMID26880542
PMCPMC4803185
OpenAlexW2291100649

What OpenQuestion holds

Textmetadata
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.