A competition model of multilineage priming and cell-fate decisions

The transition from a single cell to a body of trillions requires each cell to make fate decisions, committing to one identity among many possible options. This review aims to examine how progenitors and stem cells generate diverse fates through multilineage priming and the competitive interplay of biasing gene-expression programs. Microheterogeneity among progenitors, combined with differential fate biases, gives rise to cell populations with collective multipotency, an emergent state in which the population self-regulates to balance the production of all downstream fates during embryogenesis. We discuss how progenitor cells navigate the epigenetic landscape to control descendant cell-type proportions and how multilineage priming helps reconcile inductive, communication-driven modes of development with autonomous, self-intrinsic fate selection. In parallel, we review computational approaches that leverage single-cell transcriptomics, clonal lineage tracing, and multiomics integration to reconstruct developmental trajectories, identify biases, and dissect the mechanisms of fate selection and commitment.

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Publication Details

Journal
Cell Reports
Published
2025-12-31
DOI
https://doi.org/10.1016/j.celrep.2025.116690
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.81
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article

A competition model of multilineage priming and cell-fate decisions

Louis Faure, Ruslan Soldatov, Igor I. Adameyko, Tobias Steinschaden
1 citations
Cell Reports
Single-cell and spatial transcriptomics
0.81
article

A competition model of multilineage priming and cell-fate decisions

Louis Faure, Ruslan Soldatov, Igor I. Adameyko, Tobias Steinschaden
article en
1 citations

Abstract

The transition from a single cell to a body of trillions requires each cell to make fate decisions, committing to one identity among many possible options. This review aims to examine how progenitors and stem cells generate diverse fates through multilineage priming and the competitive interplay of biasing gene-expression programs. Microheterogeneity among progenitors, combined with differential fate biases, gives rise to cell populations with collective multipotency, an emergent state in which the population self-regulates to balance the production of all downstream fates during embryogenesis. We discuss how progenitor cells navigate the epigenetic landscape to control descendant cell-type proportions and how multilineage priming helps reconcile inductive, communication-driven modes of development with autonomous, self-intrinsic fate selection. In parallel, we review computational approaches that leverage single-cell transcriptomics, clonal lineage tracing, and multiomics integration to reconstruct developmental trajectories, identify biases, and dissect the mechanisms of fate selection and commitment.

Cell ReportsVol. 45(1)
Memorial Sloan Kettering Cancer Center (US), Medical University of Vienna (AT)
Openalex Percentile: Top 20%
Single-cell and spatial transcriptomics
0.81
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