Evidence map›Paper›PMID 39358450›Full record

ArticleNature cell biology2024

Recording morphogen signals reveals mechanisms underlying gastruloid symmetry breaking.

Harold M McNamara, Sabrina C Solley, Britt Adamson, Michelle M Chan, Jared E Toettcher

Abstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Positional information and information flows in dynamic tissues.bioRxiv : the preprint server for biology · 2026
    Article
  9. Signal control during tissue regeneration in adult animals.Nature reviews. Molecular cell biology · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Searching for physical principles of morphogenesis.Development (Cambridge, England) · 2025
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Harold M McNamaraLewis Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA. hmcnamara@princeton.edu.ORCID 0009-0006-6593-6477
Sabrina C SolleyDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID 0000-0002-2356-5608
Britt AdamsonLewis Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.ORCID 0000-0002-9451-5819
Michelle M ChanLewis Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.ORCID 0000-0001-9451-9716
Jared E ToettcherDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA. toettcher@princeton.edu.ORCID 0000-0002-1546-4030

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Center for Genomic Editing and Recording: Development and Application of Next-Generation Genome and Epigenome Editing Methods to Advance the Study and Treatment of Human DiseaseRM1HG009490 · NHGRI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI Brittany S. Adamson, Martin Joseph Ankrah Aryee · 2017 to 2026
$22.7M
Control of the 4D chromatin landscape underlying gene activity during developmentU01DK127429 · NIDDK · PRINCETON UNIVERSITY · PI GREGOR, THOMAS, LEVINE, MICHAEL STEVEN · 2020 to 2024
$3.2M
Mapping the DNA damage response in human cells with high-resolution functional genomicsR35GM138167 · NIGMS · PRINCETON UNIVERSITY · PI Brittany S. Adamson · 2020 to 2026
$2.4M
A new class of biosensors for detecting signaling dynamics without live-cell microscopyR01GM144362 · NIGMS · PRINCETON UNIVERSITY · PI TOETTCHER, JARED E · 2022 to 2025
$1.3M
Characterizing the interpretation and generation of Erk signaling dynamics using high-throughput geneticsF31HD113443 · NICHD · PRINCETON UNIVERSITY · PI Sabrina Solley · 2024 to 2026
$101k
NHGRI NIH HHS RM1 HG009490NICHD NIH HHS F31 HD113443NIDDK NIH HHS U01 DK127429NIGMS NIH HHS R01 GM144362NIGMS NIH HHS R35 GM138167NIGMS NIH HHS T32 GM007388NSF | Directorate for Biological Sciences (BIO) 2134935NSF | Directorate for Mathematical & Physical Sciences | Division of Physics (PHY) 1734030U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) U01DK127429U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) T32GM007388
6 · The paper itself

Abstract

Aggregates of stem cells can break symmetry and self-organize into embryo-like structures with complex morphologies and gene expression patterns. Mechanisms including reaction-diffusion Turing patterns and cell sorting have been proposed to explain symmetry breaking but distinguishing between these candidate mechanisms of self-organization requires identifying which early asymmetries evolve into subsequent tissue patterns and cell fates. Here we use synthetic 'signal-recording' gene circuits to trace the evolution of signalling patterns in gastruloids, three-dimensional stem cell aggregates that form an anterior-posterior axis and structures resembling the mammalian primitive streak and tailbud. We find that cell sorting rearranges patchy domains of Wnt activity into a single pole that defines the gastruloid anterior-posterior axis. We also trace the emergence of Wnt domains to earlier heterogeneity in Nodal activity even before Wnt activity is detectable. Our study defines a mechanism through which aggregates of stem cells can form a patterning axis even in the absence of external spatial cues.

Indexed as

Body PatterningGene Expression Regulation, DevelopmentalAnimalsCell AggregationGastrulaGene Regulatory NetworksNodal ProteinOrganoidsSignal TransductionStem CellsWnt ProteinsWnt Signaling PathwayNodal ProteinWnt Proteins

Identifiers

PMID39358450
PMCPMC11806519

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.