細胞の「進化の記録」推定の新手法開発に成功 -発生生物学、再生医療、老化研究への応用に期待-

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2026-08-25 理化学研究所

理化学研究所などの国際共同研究グループは、1細胞RNAシーケンス(scRNA-seq)データから正常細胞に自然に蓄積した体細胞変異を推定し、細胞の「進化の記録」として細胞系譜と細胞多様性を再構築する新しい解析手法を開発した。細胞分裂時に生じる体細胞変異は子孫細胞へ受け継がれるため、細胞間の祖先・子孫関係を示す目印になる。研究チームは、scRNA-seqから検出した変異を基に細胞間の遺伝距離を算出し、分子系統学の手法を適用して細胞系譜を推定した。シミュレーションでは、十分な変異数があれば高精度に系譜を再構築できることを確認し、ヒト胎盤の実データでも細胞型に対応する系統的な分岐構造を再現した。さらに遺伝子発現情報と統合することで、細胞の系統関係と多様性を同時に解析できた。既存のscRNA-seqデータを活用できるため、発生、再生医療、老化、がん進化などにおける細胞運命の理解を進める新たな解析基盤として期待される。

細胞の「進化の記録」推定の新手法開発に成功 -発生生物学、再生医療、老化研究への応用に期待-
1細胞RNA配列データから正常組織の細胞系譜と細胞多様性を再構築する新手法を開発

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単一細胞トランスクリプトームデータにおける体細胞変異からの細胞多様性および細胞系統の再構築 Reconstruction of cell diversity and cell lineages from somatic mutations in single-cell transcriptomic data

Satoshi Oota,Kuniya Abe,Cheng-Tsung Pan,Hideo Yokota,Wen-Hsiung Li,Kazuho Ikeo
DNA Research  Published::25 August 2026
DOI:https://doi.org/10.1093/dnares/dsag007

Abstract

Single-cell RNA sequencing (scRNA-seq) enables high-resolution profiling of individual cells. However, inferring temporal relationships among cells remains a challenge. Here, we present real-time course analysis (RTCA), a simple direct phylogenetic signal framework that reconstructs cell lineages from somatic variants detected across cells using variants derived from nuclear-encoded transcripts in scRNA-seq data. Our simulations demonstrate that only a modest increase in informative variant sites is sufficient to maintain accurate tree reconstruction, even with a tenfold increase in the number of cells. This scalability makes RTCA applicable to datasets generated by recent single-cell sequencing technologies and is also suitable for reanalyzing existing datasets. We also performed a comparative analysis between our method and a representative genotype-mediated inference framework, PhylinSic, which shares certain conceptual similarities with RTCA. The simulation results show that RTCA is more robust to sparse mutation signals and dropout-induced missing data than PhylinSic. In an application to the datasets from 2 healthy human placental samples, RTCA successfully reconstructed bifurcating phylogenetic trees. By mapping expression-based cell type clusters onto the trees, we evaluated the degree of monophyly within lineages and found our results consistent with known placental differentiation pathways. The identified cell lineages also aligned with classifications based on gene expression and pseudotime analysis. Compared to gene expression-based and pseudotime analysis, RTCA provides a temporally based model of cell trajectories, integrating lineage and expression information in a biologically meaningful manner. In summary, RTCA offers a scalable, cost-effective solution for reconstructing developmental processes in complex normal tissues.

細胞遺伝子工学
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