基线:用于哺乳动物单细胞谱系追踪的CRISPR碱基编辑平台。

Evan Winter, Francesco Emiliani, Aidan Cook, Asma Abderrahim, Aaron Henrik McKenna
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引用次数: 0

摘要

细胞的命运是由其遗传状态或谱系以及不断变化的环境所决定的。基于crispr的记录技术是一种很有前途的解决方案,可以绘制发育系统的谱系图,但单细胞恢复、工程复杂性和规模方面的挑战仍然存在。在这里,我们介绍BASELINE,它使用碱基编辑与单细胞分析一起生成高分辨率谱系树。BASELINE使用Cas12a腺嘌呤碱基编辑器对50个合成靶点内的核苷酸进行不可逆编辑,这些靶点被多次整合到细胞基因组中。我们发现BASELINE在广泛的生物学相关间隔内积累谱系特异性标记,在胰腺癌模型中记录超过4300位信息,比现有技术增加了50倍。单细胞测序揭示了这些记录的高保真捕获,在哺乳动物发育的估计范围内,恢复了高达40个细胞分裂深度的谱系重建。我们期望BASELINE应用于发展和疾病中的广泛的谱系追踪项目,特别是在细胞工程使小的、更分布式的系统具有挑战性的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BASELINE: A CRISPR Base Editing Platform for Mammalian-Scale Single-Cell Lineage Tracing.

A cells fate is shaped by its inherited state, or lineage, and the ever-shifting context of its environment. CRISPR-based recording technologies are a promising solution to map the lineage of a developing system, yet challenges remain regarding single-cell recovery, engineering complexity, and scale. Here, we introduce BASELINE, which uses base editing to generate high-resolution lineage trees in conjunction with single-cell profiling. BASELINE uses the Cas12a adenine base editor to irreversibly edit nucleotides within 50 synthetic target sites, which are integrated multiple times into a cells genome. We show that BASELINE accumulates lineage-specific marks over a wide range of biologically relevant intervals, recording more than 4300 bits of information in a model of pancreatic cancer, a 50X increase over existing technologies. Single-cell sequencing reveals high-fidelity capture of these recorders, recovering lineage reconstructions up to 40 cell divisions deep, within the estimated range of mammalian development. We expect BASELINE to apply to a wide range of lineage-tracing projects in development and disease, especially in which cellular engineering makes small, more distributed systems challenging.

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