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利用Cas9和Cas12a进行双核酸酶单细胞谱系追踪

Dual-nuclease single-cell lineage tracing by Cas9 and Cas12a.

作者信息

Chen Cheng, Liao Yuanxin, Zhu Miao, Wang Li, Yu Xinran, Li Meishi, Peng Guangdun

机构信息

Center for Cell Lineage Technology and Engineering, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangdong-Hong Kong Joint Laboratory for Stem Cell and Regenerative Medicine, GIBH-CUHK Joint Research Laboratory on Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, China-New Zealand Belt and Road Joint Laboratory on Biomedicine and Health, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.

Center for Cell Lineage Technology and Engineering, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangdong-Hong Kong Joint Laboratory for Stem Cell and Regenerative Medicine, GIBH-CUHK Joint Research Laboratory on Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, China-New Zealand Belt and Road Joint Laboratory on Biomedicine and Health, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China; University of Chinese Academy of Sciences, Beijing, China.

出版信息

Cell Rep. 2025 Jan 28;44(1):115105. doi: 10.1016/j.celrep.2024.115105. Epub 2024 Dec 24.

DOI:10.1016/j.celrep.2024.115105
PMID:39721023
Abstract

Single-cell lineage tracing based on CRISPR-Cas9 gene editing enables the simultaneous linkage of cell states and lineage history at a high resolution. Despite its immense potential in resolving the cell fate determination and genealogy within an organism, existing implementations of this technology suffer from limitations in recording capabilities and considerable barcode dropout. Here, we introduce DuTracer, a versatile tool that utilizes two orthogonal gene editing systems to record cell lineage history at single-cell resolution in an inducible manner. DuTracer shows the ability to enhance lineage recording with minimized target dropouts and potentially deeper tree depths. Applying DuTracer in mouse embryoid bodies and neuromesodermal organoids illustrates the lineage relationship of different cell types and proposes potential lineage-biased molecular drivers, showcased by identifying transcription factor Foxb1 as a modulator in the cell fate determination of neuromesodermal progenitors. Collectively, DuTracer facilitates the precise and regulatory interrogation of cellular lineages of complex biological processes.

摘要

基于CRISPR-Cas9基因编辑的单细胞谱系追踪能够在高分辨率下同时将细胞状态与谱系历史联系起来。尽管该技术在解析生物体内细胞命运决定和谱系方面具有巨大潜力,但现有技术在记录能力方面存在局限性,且存在大量条形码丢失的问题。在此,我们介绍DuTracer,这是一种多功能工具,它利用两个正交基因编辑系统以诱导方式在单细胞分辨率下记录细胞谱系历史。DuTracer显示出增强谱系记录的能力,同时将靶点丢失降至最低,并可能实现更深的谱系树深度。将DuTracer应用于小鼠胚胎体和神经中胚层类器官,阐明了不同细胞类型的谱系关系,并提出了潜在的谱系偏向分子驱动因素,通过鉴定转录因子Foxb1作为神经中胚层祖细胞命运决定中的调节因子得以体现。总的来说,DuTracer有助于对复杂生物过程的细胞谱系进行精确和调控性研究。

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