Evidence map›Paper›PMID 41396982›Full record

ArticlePLoS computational biology2025

Assessing the relative contributions of mosaic and regulatory developmental modes from single-cell trajectories.

Solène Song, Paul Villoutreix

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Solène SongAix-Marseille Université, MMG, INSERM U1251, Turing Centre for Living Systems, Marseille, France.ORCID 0000-0003-0122-0489
Paul VilloutreixAix-Marseille Université, MMG, INSERM U1251, Turing Centre for Living Systems, Marseille, France.ORCID 0000-0002-6333-5735

Funding

Aix-Marseille UniversityFrench National Research Agency
6 · The paper itself

Abstract

Development is a complex process driven by coordinated cell proliferation, differentiation, and spatial organization. Classically, two ways to specify cell types during development have been hypothesized: the mosaic and regulative modes. In the mosaic mode, a particular cell isolated from the rest of the embryo will still give rise to progeny with the same fate as expected in normal development, relying on lineage-inherited factors. In contrast, in the regulative mode, the fate of a cell depends on its interactions with its environment and thus relies on space-dependent factors. While both modes often co-exist, their relative contributions remain poorly quantified at single-cell resolution. We present a novel approach to measure these contributions from single-cell data from C. elegans development. The invariant lineage of C. elegans allows the integration of spatial positions, lineage relationships, and protein expression data. Using single-cell protein expression profiles as a readout of cell state, we define two quantifiable metrics: 1) a proxy for the contribution of the mosaic mode, computed as the strength of the relationship between the cell-cell lineage distance and the cell-cell expression distance, 2) a proxy for the contribution of the regulative mode, computed as the strength of the relationship between the cell-cell context distance - capturing spatial neighborhood similarity - and the cell-cell expression distance. To validate these metrics, we compared empirical results from C. elegans to artificial models with defined developmental rules. Our analysis reveals the coexistence of mosaic and regulative modes, with their relative contributions varying across tissues and developmental stages. For example, in skin tissue, the mosaic mode dominates in early development, while the regulative mode prevails later. Our approach offers a quantitative, unbiased, and perturbation-free method to study fundamental principles of developmental biology.

Indexed as

Caenorhabditis elegansSingle-Cell AnalysisAnimalsCaenorhabditis elegans ProteinsCell DifferentiationCell LineageComputational BiologyGene Expression Regulation, DevelopmentalModels, BiologicalMosaicismCaenorhabditis elegans Proteins

Identifiers

PMID41396982
PMCPMC12721551

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LicenceCC BY
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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.