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Peijie Zhou1,2,3,4, Federico Bocci1, Tiejun Li5

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Summary
This summary is machine-generated.

Spatial transcriptomics and messenger RNA splicing reveal cell state dynamics. The new spatial transition tensor (STT) method reconstructs cell-state-specific transitions and dynamics across spatiotemporal scales.

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Area of Science:

  • Computational Biology
  • Genomics
  • Developmental Biology

Background:

  • Spatial transcriptomics and mRNA splicing provide spatiotemporal information on cell states and transitions.
  • Existing lineage-inference methods often lack spatial dynamics or cannot capture multiple cell state transition paths.

Purpose of the Study:

  • To develop a novel method, spatial transition tensor (STT), for characterizing multistability in space using spatial transcriptomes and mRNA splicing.
  • To reconstruct cell-state-specific dynamics and spatial state transitions across multiple spatiotemporal scales.

Main Methods:

  • Utilized a multiscale dynamical model incorporating mRNA splicing and spatial transcriptomes.
  • Employed a four-dimensional transition tensor and spatial-constrained random walk for analysis.
  • Reconstructed cell-state-specific dynamics and spatial transitions through short-time local tensor streamlines and long-time transition paths.

Main Results:

  • Benchmarking and applications on diverse transcriptome datasets demonstrated STT's capability.
  • Successfully recovered cell-state-specific dynamics and associated genes missed by existing methods.
  • Validated STT on epithelial-mesenchymal transitions, blood development, mouse brain, and chicken heart development.

Conclusions:

  • STT offers a robust method for analyzing spatiotemporal dynamics in single-cell transcriptomics.
  • Provides a consistent multiscale description of single-cell transcriptome data.
  • Enhances understanding of cell state transitions and their underlying gene regulation across biological systems.