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一种用于检测人细胞中由CRISPR/Cas9和单链寡脱氧核苷酸催化的点突变修复作用下的现场诱变性的标准方法。

A Standard Methodology to Examine On-site Mutagenicity As a Function of Point Mutation Repair Catalyzed by CRISPR/Cas9 and SsODN in Human Cells.

作者信息

Rivera-Torres Natalia, Kmiec Eric B

机构信息

Gene Editing Institute, Helen F. Graham Cancer Center and Research Institute, Christiana Care Health Services; Department of Medical Sciences, University of Delaware.

Gene Editing Institute, Helen F. Graham Cancer Center and Research Institute, Christiana Care Health Services; Department of Medical Sciences, University of Delaware;

出版信息

J Vis Exp. 2017 Aug 25(126):56195. doi: 10.3791/56195.

Abstract

Combinatorial gene editing using CRISPR/Cas9 and single-stranded oligonucleotides is an effective strategy for the correction of single-base point mutations, which often are responsible for a variety of human inherited disorders. Using a well-established cell-based model system, the point mutation of a single-copy mutant eGFP gene integrated into HCT116 cells has been repaired using this combinatorial approach. The analysis of corrected and uncorrected cells reveals both the precision of gene editing and the development of genetic lesions, when indels are created in uncorrected cells in the DNA sequence surrounding the target site. Here, the specific methodology used to analyze this combinatorial approach to the gene editing of a point mutation, coupled with a detailed experimental strategy to measuring indel formation at the target site, is outlined. This protocol outlines a foundational approach and workflow for investigations aimed at developing CRISPR/Cas9-based gene editing for human therapy. The conclusion of this work is that on-site mutagenesis takes place as a result of CRISPR/Cas9 activity during the process of point mutation repair. This work puts in place a standardized methodology to identify the degree of mutagenesis, which should be an important and critical aspect of any approach destined for clinical implementation.

摘要

使用CRISPR/Cas9和单链寡核苷酸进行组合基因编辑是校正单碱基点突变的有效策略,这些突变常常导致多种人类遗传性疾病。利用一个成熟的基于细胞的模型系统,采用这种组合方法修复了整合到HCT116细胞中的单拷贝突变eGFP基因的点突变。对校正和未校正细胞的分析揭示了基因编辑的精确性以及当在靶位点周围的DNA序列中未校正细胞中产生插入缺失时遗传损伤的发生情况。在此,概述了用于分析这种针对点突变进行基因编辑的组合方法的具体方法,以及用于测量靶位点插入缺失形成的详细实验策略。本方案概述了旨在开发基于CRISPR/Cas9的人类治疗基因编辑的研究的基础方法和工作流程。这项工作的结论是,在点突变修复过程中,由于CRISPR/Cas9的活性会发生原位诱变。这项工作建立了一种标准化方法来确定诱变程度,这应该是任何旨在临床应用的方法的一个重要且关键的方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/430d/5614406/67847d25542b/jove-126-56195-4.jpg

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