干细胞分化和肿瘤进化的单细胞系统动力学推断。

Kun Wang, Zhaolian Lu, Zeqi Yao, Xionglei He, Zheng Hu, Da Zhou
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引用次数: 0

摘要

系统动力学推断(PI)利用系统发生树来量化种群动态和进化轨迹。单细胞谱系追踪可以重建多细胞生物中数千个细胞的系统发育树,促进细胞水平的PI。然而,细胞分化和体细胞进化挑战了现有PI框架在体细胞组织中的直接应用。我们介绍了scPhyloX,这是一个计算框架,通过利用单细胞系统发育树来推断组织发育和肿瘤进化动力学来建模结构细胞群体。一个关键的进步是它能够推断时变参数,捕捉动态的生物过程。模拟证明了scPhyloX在组织发育、疾病治疗和肿瘤生长等场景中的准确性。对三个真实数据集的应用揭示了体细胞动力学的见解:苍蝇器官发育中的循环干细胞超调,人类衰老过程中多能造血祖细胞的克隆扩增,以及早期结直肠肿瘤发生中的明显亚克隆选择。因此,scPhyloX为研究体细胞组织的发育和进化提供了一种计算方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-cell phylodynamic inference of stem cell differentiation and tumor evolution.

Phylodynamic inference (PI) quantifies population dynamics and evolutionary trajectories using phylogenetic trees. Single-cell lineage tracing enables phylogenetic tree reconstruction for thousands of cells in multicellular organisms, facilitating PI at the cellular level. However, cell differentiation and somatic evolution challenge the direct application of existing PI frameworks to somatic tissues. We introduce scPhyloX, a computational framework modeling structured cell populations by leveraging single-cell phylogenetic trees to infer tissue development and tumor evolution dynamics. A key advancement is its ability to infer time-varying parameters, capturing dynamic biological processes. Simulations demonstrate scPhyloX's accuracy in scenarios including tissue development, disease treatment, and tumor growth. Application to three real datasets reveals insights into somatic dynamics: cycling stem cell overshoot in fly organ development, clonal expansion of multipotent hematopoietic progenitors during human aging, and pronounced subclonal selection in early colorectal tumorigenesis. scPhyloX thus provides a computational approach for investigating somatic tissue development and evolution.

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