Dynamic Landscape Analysis of cell fate decisions provides predictive models of neural development from single-cell data
Building a mechanistic understanding of cell fate decisions remains a fundamental goal of developmental biology, with implications for stem cell therapies, regenerative medicine and understanding disease mechanisms. Single-cell transcriptomics provides a detailed picture of the cellular states observed during these decisions, but building dynamic and predictive models from these data remains a challenge. Here, we present dynamic landscape analysis (DLA), an integrative framework that applies dynamical systems theory to identify stable cell states, map transition pathways, and generate a predictive cell fate decision landscape from single-cell data. Applying this framework to vertebrate neural tube development revealed that progenitor specification by Sonic Hedgehog (Shh) can be captured in a landscape with an unexpected topology in which initially divergent lineages converge to the same fate through multiple distinct routes. The model accurately predicted cellular responses and cell fate allocation for unseen dynamic signalling regimes. Cross-species validation using human embryonic organoid data demonstrated conservation of this decision-making architecture. By modelling the dynamic responses that drive cell fate decisions, the DLA framework provides a quantitative and generative framework for extracting mechanistic insights from high-dimensional single-cell data.
Authors
- M. Joaquina Delás (ORCID: https://orcid.org/0000-0001-9727-9068)
- James Briscoe (ORCID: https://orcid.org/0000-0002-1020-5240)
- Rory J. Maizels (ORCID: https://orcid.org/0000-0001-6027-3746)
- Meritxell Sáez (ORCID: https://orcid.org/0000-0002-2991-3183)
- Marine Fontaine (ORCID: https://orcid.org/0000-0002-5993-5842)
- Elizabeth Finnie
- David A. Rand
Institutions
- The Francis Crick Institute (GB)
- University of Warwick (GB)
- Universitat Ramon Llull (ES)
Publication Details
- Journal
- PLoS Biology
- Published
- 2026-08-26
- DOI
- https://doi.org/10.1371/journal.pbio.3003953
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- Wellcome Trust
- Francis Crick Institute
- Cancer Research UK
- Medical Research Council
- Engineering and Physical Sciences Research Council
- Kavli Institute for Theoretical Physics, University of California, Santa Barbara