Evidence map›Paper›PMID 40251161›Full record

ArticleNature communications2025

Cell lineage-resolved embryonic morphological map reveals signaling associated with cell fate and size asymmetry.

Guoye Guan, Zelin Li, Yiming Ma, Pohao Ye, Jianfeng Cao, Ming-Kin Wong, Vincy Wing Sze Ho, Lu-Yan Chan, Hong Yan, Chao Tang and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Transcriptomic profiling of the embryonicbioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

11 authors.

Guoye Guan *Center for Quantitative Biology, Peking University, Beijing, China.ORCID http://orcid.org/0000-0003-4479-4722
Zelin Li *Department of Electrical Engineering, City University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-0985-8420
Yiming Ma *Department of Biology, Hong Kong Baptist University, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-3646-3619
Pohao Ye *Department of Biology, Hong Kong Baptist University, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-7828-2592
Jianfeng CaoDepartment of Electrical Engineering, City University of Hong Kong, Hong Kong SAR, China.
Ming-Kin WongDepartment of Biology, Hong Kong Baptist University, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-4088-3819
Vincy Wing Sze HoDepartment of Biology, Hong Kong Baptist University, Hong Kong SAR, China.
Lu-Yan ChanDepartment of Biology, Hong Kong Baptist University, Hong Kong SAR, China.
Hong YanDepartment of Electrical Engineering, City University of Hong Kong, Hong Kong SAR, China. h.yan@cityu.edu.hk.ORCID http://orcid.org/0000-0001-9661-3095
Chao TangCenter for Quantitative Biology, Peking University, Beijing, China. tangc@pku.edu.cn.ORCID http://orcid.org/0000-0003-1474-3705
Zhongying ZhaoDepartment of Biology, Hong Kong Baptist University, Hong Kong SAR, China. zyzhao@hkbu.edu.hk.ORCID http://orcid.org/0000-0003-2743-9008

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

How cells change shape is crucial for the development of tissues, organs and embryos. However, studying these shape changes in detail is challenging. Here we present a comprehensive real-time cellular map that covers over 95% of the cells formed during Caenorhabditis elegans embryogenesis, featuring nearly 400,000 3D cell regions. This map includes information on each cell's identity, lineage, fate, shape, volume, surface area, contact area, and gene expression profiles, all accessible through our user-friendly software and website. Our map allows for detailed analysis of key developmental processes, including dorsal intercalation, intestinal formation, and muscle assembly. We show how Notch and Wnt signaling pathways, along with mechanical forces from cell interactions, regulate cell fate decisions and size asymmetries. Our findings suggest that repeated Notch signaling drives size disparities in the large excretory cell, which functions like a kidney. This work sets the stage for in-depth studies of the mechanisms controlling cell fate differentiation and morphogenesis.

Indexed as

Caenorhabditis elegansCell LineageEmbryo, NonmammalianAnimalsCaenorhabditis elegans ProteinsCell DifferentiationCell ShapeCell SizeEmbryonic DevelopmentGene Expression Regulation, DevelopmentalMorphogenesisReceptors, NotchSignal TransductionWnt Signaling PathwayCaenorhabditis elegans ProteinsReceptors, Notch

Identifiers

PMID40251161
PMCPMC12008310

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.