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Detection of Somatic Point Mutations Directly from Spatial Transcriptomics Enables in vivo Spatiotemporal Lineage Tracing

Yang, Z.; Yao, M.; Yang, Q.; Du, Y.; Lu, J.; Wu, X.; Lin, J.; Qian, Z.; Hu, S.; Xia, Y.; Liu, H.; Zhou, Q.; Ma, X.; Luo, Y.; Fan, W.; Pei, W.; Xia, Y.; Yu, X.; Luan, J.; Zhang, Q.; Zhang, Y.; Wang, Q.; Zeng, J.; Zhang, Y.; Wu, W.; Dou, Y.

2026-02-06 bioinformatics
10.64898/2026.02.04.703493 bioRxiv
Show abstract

Spatial transcriptomics reveals tissue organization but lacks in vivo lineage-tracing methods applicable to humans. We introduce SpaceTracer, a computational framework that accurately detects somatic single-nucleotide variants (SNVs) directly from spatial transcriptomics data. By leveraging naturally occurring somatic SNVs, SpaceTracer reconstructs cellular phylogenies within native tissue architecture, enabling the mapping of lineage spread, migration, lineage-coupled expression changes and lineage-aware local interactions. Applied to human cutaneous squamous cell carcinoma, it traced tumor initiation and progressions, uncovered widespread pre-invasive migration of dedifferentiated epithelial cells and characterized mutant B cells migrating from tertiary lymphoid structures (TLS) into the tumor boundary. The framework also reconstructed developmental lineages across multiple tissues and identified tissue-resident mutant immune cells. SpaceTracer thus provides a perturbation-free platform for high-resolution spatiotemporal lineage tracing, offering a transformative tool for elucidating complex biological systems--especially tumor-immune ecosystems--with direct implications for advancing cancer immunotherapy.

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