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定义基于 CRISPR/Cas9 的细胞谱系示踪在斑马鱼中的内源性条形码位点。

Defining endogenous barcoding sites for CRISPR/Cas9-based cell lineage tracing in zebrafish.

机构信息

State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China.

State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China.

出版信息

J Genet Genomics. 2020 Feb 20;47(2):85-91. doi: 10.1016/j.jgg.2019.11.012. Epub 2020 Feb 7.

Abstract

There is a growing interest in developing experimental methods for tracking the developmental cell lineages of a complex organism. The recently developed CRISPR/Cas9-based barcoding method is, although highly promising, difficult to scale up because it relies on exogenous barcoding sequences that are engineered into the genome. In this study, we characterized 78 high-quality endogenous sites in the zebrafish genome that can be used as CRISPR/Cas9-based barcoding sites. The 78 sites are all highly expressed in most of the cell types according to single-cell RNA sequencing (scRNA-seq) data. Hence, the barcoding information of the 78 endogenous sites is recovered by the available scRNA-seq platforms, enabling simultaneous characterization of cell type and cell lineage information.

摘要

人们对开发用于跟踪复杂生物发育细胞谱系的实验方法越来越感兴趣。最近开发的基于 CRISPR/Cas9 的条形码方法虽然很有前途,但由于它依赖于工程化到基因组中的外源条形码序列,因此难以扩展。在这项研究中,我们对斑马鱼基因组中的 78 个高质量的内源性位点进行了特征描述,这些位点可作为基于 CRISPR/Cas9 的条形码位点。根据单细胞 RNA 测序 (scRNA-seq) 数据,这 78 个位点在大多数细胞类型中均高度表达。因此,通过现有的 scRNA-seq 平台可以恢复 78 个内源性位点的条形码信息,从而能够同时对细胞类型和细胞谱系信息进行特征描述。

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