Evidence map›Paper›PMID 41364758›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Generative epigenetic landscapes map the topology and topography of cell fates.

Victoria Mochulska, Paul François

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Victoria MochulskaDepartment of Physics, McGill University, Montréal, QC H3A 2T8, Canada.ORCID 0000-0002-1765-6132
Paul FrançoisDépartement de Biochimie et Medecine Moléculaire, Université de Montréal, Montréal, QC H3T 1J4, Canada.ORCID 0000-0002-2223-839X

Funding

Canadian Institutes of Health Research (CIHR) RN509976Fonds Courtois 0Fonds de recherche du Québec (FRQ) 328292Natural Sciences and Engineering Research Council of Canada (NSERC) RGPIN-2023-03843
6 · The paper itself

Abstract

Epigenetic landscapes were proposed by Waddington as the central concept to describe cell fate dynamics in a locally low-dimensional space. In modern landscape models, attractors represent cell types, and stochastic jumps and bifurcations drive cellular decisions, allowing for quantitative and predictive descriptions. However, given a biological problem of interest, we still lack tools to infer and build possible Waddington landscapes systematically. In this study, we propose a generative model for deriving epigenetic landscapes compatible with data. To build the landscapes, we combine gradient and rotational vector fields composed of locally weighted elements that encode "valleys" of the Waddington landscape, resulting in interpretable models. We optimize landscapes through computational evolution and illustrate our approach with two developmental examples: metazoan segmentation and neuromesoderm differentiation. In both cases, we obtain ensembles of solutions that reveal both known and original landscapes in terms of topology and bifurcations. Conversely, topographic features appear strongly constrained by dynamical data, which suggests that our approach can generically derive interpretable and predictive epigenetic landscapes.

Indexed as

Cell DifferentiationCell LineageEpigenesis, GeneticModels, GeneticAnimalscellular differentiationdynamical systemsevolutionmathematical modelingWaddington landscape

Identifiers

PMID41364758
PMCPMC12718394

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Registered trials

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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.