In vitro analysis of site specific nuclease selectivity by NGS

IF 1 Q4 ENGINEERING, BIOMEDICAL AIMS Bioengineering Pub Date : 2021-01-01 DOI:10.3934/bioeng.2021020
V. Brondani
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Abstract

Nucleases currently used in genome engineering induce hydrolysis of DNA phosphate backbone in a sequence-specific manner. The RNA guided nucleases describe today are recognizing a sequence with two distinct molecular interactions: first, like a restriction endonuclease, by direct interaction between the protein and the DNA; and second, by hybridization of the guide RNA with the target DNA sequence. Here we report an in vitro assay to assess the cleavage specificity and the selectivity of the nucleases. The assay is designed using a plasmid encompassing the DNA target site degenerated at positions determined on structural feature. The results demonstrate that the Cpf1 RNA guided nuclease is highly specific for the target sequence, nevertheless its substrate selectivity is low compare to a restriction endonuclease.
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NGS法分析位点特异性核酸酶的体外选择性
目前用于基因组工程的核酸酶以序列特异性的方式诱导DNA磷酸主链的水解。目前所描述的RNA引导核酸酶是识别具有两种不同分子相互作用的序列:首先,像限制性内切酶一样,通过蛋白质和DNA之间的直接相互作用;第二,将引导RNA与目标DNA序列杂交。在这里,我们报告了一个体外实验,以评估裂解特异性和选择性的核酸酶。该分析是设计使用包含在结构特征上确定的位置退化的DNA靶位点的质粒。结果表明,Cpf1 RNA引导的核酸酶对目标序列具有高度特异性,但与限制性内切酶相比,其底物选择性较低。
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来源期刊
AIMS Bioengineering
AIMS Bioengineering ENGINEERING, BIOMEDICAL-
自引率
0.00%
发文量
17
审稿时长
4 weeks
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