CellPolaris: Transfer Learning for Gene Regulatory Network Construction to Guide Cell State Transitions
Cell fate decisions are orchestrated by intricate gene regulatory networks (GRNs), which govern gene expression with precise spatiotemporal control. However, accurately capturing context-specific nature of gene regulation remains challenging, particularly when integrating multi-omics data at bulk and single-cell level across diverse cellular contexts. Here, we present CellPolaris, a unified computational framework designed to decode the roles of transcription factors (TFs) in developmental processes. CellPolaris performs TF-centered GRN construction, master TF identification, and TF perturbation simulation. By leveraging transfer learning, the framework generates tissue-specific or cell-type-specific GRNs using pre-constructed high-confidence GRNs of diverse contexts and requires only transcriptomic data as input. Using these learned GRNs, CellPolaris identifies underlying master TFs critical for cell fate transitions and simulates the effects of TF perturbations on developmental processes. Benchmarking tests demonstrate the robust performance of CellPolaris in GRN construction. The efficacy of CellPolaris is supported by the significant overlap between predicted top-ranked master regulators and known TF combinations experimentally validated in cell fate conversion experiments. Furthermore, CellPolaris accurately simulates the developmental consequences of Rfx2 knockout during round spermatid differentiation. In summary, we present CellPolaris, a comprehensive framework that enables GRN construction through transfer learning, identification of key TFs driving cell fate transitions, and simulation of TF perturbations. This tool allows us to further elucidate the regulatory mechanisms underlying developmental processes and cell state transitions.
Authors
- Shirui Li (ORCID: https://orcid.org/0000-0001-9506-133X)
- Y. Zhang
- Xuezhi Wang (ORCID: https://orcid.org/0000-0003-1822-7732)
- Yana Liu (ORCID: https://orcid.org/0000-0002-9101-9772)
- Ming‐Han Tong (ORCID: https://orcid.org/0000-0002-1967-5927)
- Yao Tian
- Shihua Zhang (ORCID: https://orcid.org/0000-0003-0192-7118)
- Yuanchun Zhou (ORCID: https://orcid.org/0000-0001-6646-9352)
- Jingxi Dong (ORCID: https://orcid.org/0009-0001-2017-584X)
- Xinlong Jiang
- Wentao Cui (ORCID: https://orcid.org/0000-0002-1404-3971)
- Wenhao Liu (ORCID: https://orcid.org/0009-0005-7006-9921)
- Chen Yao (ORCID: https://orcid.org/0000-0001-6852-5661)
- Xin Qin
- Guihai Feng
- Zhenpeng Man
- Yanru Wang (ORCID: https://orcid.org/0000-0001-8272-2450)
- Ping Xu
- Guole Liu
- Wuliang Huang
- Xin Li
- Ge Yang
- Xiaodong Yang
- Jiahao Zhang
- Yiqiang Chen
- Hongmei Wang
- Pengfei Wang
- Zhongming Liang
Institutions
- Yunnan University (CN)
- Chinese Academy of Sciences (CN)
- Institute for Stem Cell Biology and Regenerative Medicine (IN)
- Institute of Computing Technology (CN)
- Shandong Institute of Automation (CN)
- Beijing Academy of Artificial Intelligence (CN)
- Computer Network Information Center (CN)
- Academy of Mathematics and Systems Science (CN)
- Center for Excellence in Molecular Cell Science (CN)
- University of Chinese Academy of Sciences (CN)
- Institute of Zoology (CN)
Publication Details
- Journal
- Advanced Science
- Published
- 2026-01-07
- DOI
- https://doi.org/10.1002/advs.202508697
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00