首页> 外国专利> METHOD FOR DETECTING OFF-TARGET EFFECT OF ADENINE BASE EDITOR SYSTEM BASED ON WHOLE-GENOME SEQUENCING AND USE THEREOF IN GENE EDITING

METHOD FOR DETECTING OFF-TARGET EFFECT OF ADENINE BASE EDITOR SYSTEM BASED ON WHOLE-GENOME SEQUENCING AND USE THEREOF IN GENE EDITING

机译:基于全基因组测序的腺嘌呤基础编辑器系统的脱靶效应的方法及其在基因编辑中的使用

摘要

The present invention provide a method for detecting the genome-wide off-target effects of adenine base editor (ABE) and the application in gene editing thereof. ABE comprises the TadA:TadA*:Cas9 fusion protein and gRNA which is able to catalyze the substitution of A to G with high efficiency at the target site, which can bring ABE a bright application prospect in gene editing and construction of disease model for human disease. Thus, the present invention provides the EndoV-seq method first time to detect the genome-wide off-target effects of ABE. The EndoV-seq method has a wide application prospect in gene editing, especially in gene editing for treatment field of human disease.
机译:本发明提供了一种检测腺嘌呤碱基编辑器(ABE)的基因组偏移偏移的方法及其在基因编辑中的应用。 ABE包括TADA:TADA *:CAS9融合蛋白和GRNA,其能够在靶位点催化效率的高效率,这可以使ABE在基因编辑和人类疾病模型的构建中提出明亮的应用前景 疾病。 因此,本发明提供了ENDOV-SEQ方法首次检测ABE的基因组偏差效应。 EndoV-SEQ方法具有广泛的基因编辑应用前景,特别是在人类疾病治疗领域的基因编辑中。

著录项

  • 公开/公告号US2021395812A1

    专利类型

  • 公开/公告日2021-12-23

    原文格式PDF

  • 申请/专利权人 SUN YAT-SEN UNIVERSITY;

    申请/专利号US201917279124

  • 发明设计人 ZHOU SONGYANG;PUPING LIANG;JUNJIU HUANG;

    申请日2019-09-23

  • 分类号C12Q1/6869;

  • 国家 US

  • 入库时间 2022-08-24 22:59:44

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