OneSC:重现细胞状态转换的计算平台。

Da Peng, Patrick Cahan
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引用次数: 0

摘要

动机细胞状态转换的计算建模一直是发育生物学、癌症生物学和细胞命运工程学领域许多人的极大兴趣所在,因为它能比在实验室中更快速、更廉价地进行扰动实验。单细胞 RNA 测序(scRNA-seq)技术的最新进展可以捕捉细胞沿时间轨迹转变时的高分辨率快照。利用这些高通量数据集,我们可以训练计算模型,生成能忠实模拟时间轨迹的硅学 "合成 "细胞:在这里,我们介绍 OneSC,这是一个可以利用由核心转录因子(TFs)调控网络支配的随机微分方程系统模拟细胞状态转换的平台。与当前的许多网络推断方法不同,OneSC优先考虑生成布尔网络,以产生忠实的细胞状态转换和终端细胞状态,从而模拟真实的生物系统。我们将 OneSC 应用于真实数据,利用小鼠髓系祖细胞 scRNA-seq 数据集推断出核心 TF 网络,并证明该网络的动态模拟生成的合成单细胞表达谱忠实再现了进入分化细胞状态(红细胞、巨核细胞、粒细胞和单核细胞)的四种髓系分化轨迹。最后,通过对小鼠髓系祖细胞核心网络进行硅学扰动,我们发现 OneSC 可以准确预测 TF 扰动的细胞命运决定偏差,这与之前的实验观察结果非常吻合:OneSC以Python软件包的形式在GitHub (https://github.com/CahanLab/oneSC) 和Zenodo (https://zenodo.org/records/14052421)上实现。补充信息:补充数据可在 Bioinformatics online 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
OneSC: A computational platform for recapitulating cell state transitions.

Motivation: Computational modelling of cell state transitions has been a great interest of many in the field of developmental biology, cancer biology and cell fate engineering because it enables performing perturbation experiments in silico more rapidly and cheaply than could be achieved in a lab. Recent advancements in single-cell RNA sequencing (scRNA-seq) allow the capture of high-resolution snapshots of cell states as they transition along temporal trajectories. Using these high-throughput datasets, we can train computational models to generate in silico 'synthetic' cells that faithfully mimic the temporal trajectories.

Results: Here we present OneSC, a platform that can simulate cell state transitions using systems of stochastic differential equations govern by a regulatory network of core transcription factors (TFs). Different from many current network inference methods, OneSC prioritizes on generating Boolean network that produces faithful cell state transitions and terminal cell states that mimic real biological systems. Applying OneSC to real data, we inferred a core TF network using a mouse myeloid progenitor scRNA-seq dataset and showed that the dynamical simulations of that network generate synthetic single-cell expression profiles that faithfully recapitulate the four myeloid differentiation trajectories going into differentiated cell states (erythrocytes, megakaryocytes, granulocytes and monocytes). Finally, through the in silico perturbations of the mouse myeloid progenitor core network, we showed that OneSC can accurately predict cell fate decision biases of TF perturbations that closely match with previous experimental observations.

Availability: OneSC is implemented as a Python package on GitHub (https://github.com/CahanLab/oneSC) and on Zenodo (https://zenodo.org/records/14052421).

Supplementary information: Supplementary data are available at Bioinformatics online.

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