Dissecting reversible and irreversible single cell state transitions from gene regulatory networks

Understanding cell state transitions and their governing regulatory mechanisms remains one of the fundamental questions in biology. We develop a computational method, state transition inference using cross-cell correlations (STICCC), for predicting reversible and irreversible cell state transitions at single-cell resolution by using gene expression data and a set of gene regulatory interactions. The method is inspired by the fact that the gene expression time delays between regulators and targets can be exploited to infer past and future gene expression states. From applications to both simulated and experimental single-cell gene expression data, we show that STICCC-inferred vector fields capture basins of attraction and irreversible fluxes. By connecting regulatory information with systems' dynamical behaviors, STICCC reveals how network interactions influence reversible and irreversible state transitions. Compared to existing methods that infer pseudotime and RNA velocity, STICCC provides complementary insights into the gene regulation of cell state transitions.

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Publication Details

Journal
Molecular Systems Biology
Published
2026-02-09
DOI
https://doi.org/10.1038/s44320-026-00196-8
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

Dissecting reversible and irreversible single cell state transitions from gene regulatory networks

Mingyang Lu, Daniel A Ramirez
Molecular Systems Biology
Single-cell and spatial transcriptomics
article

Dissecting reversible and irreversible single cell state transitions from gene regulatory networks

Mingyang Lu, Daniel A Ramirez
article en

Abstract

Understanding cell state transitions and their governing regulatory mechanisms remains one of the fundamental questions in biology. We develop a computational method, state transition inference using cross-cell correlations (STICCC), for predicting reversible and irreversible cell state transitions at single-cell resolution by using gene expression data and a set of gene regulatory interactions. The method is inspired by the fact that the gene expression time delays between regulators and targets can be exploited to infer past and future gene expression states. From applications to both simulated and experimental single-cell gene expression data, we show that STICCC-inferred vector fields capture basins of attraction and irreversible fluxes. By connecting regulatory information with systems' dynamical behaviors, STICCC reveals how network interactions influence reversible and irreversible state transitions. Compared to existing methods that infer pseudotime and RNA velocity, STICCC provides complementary insights into the gene regulation of cell state transitions.

Molecular Systems Biology
Northeastern University (US), Center for Theoretical Biological Physics (US)
National Science Foundation, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 62%
Single-cell and spatial transcriptomics
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Dissecting reversible and irreversible single cell state transitions from gene regulatory networks — Mingyang Lu, Daniel A Ramirez · Molecular Systems Biology (2026) | TGRS Research Map | TGRS