导论:基因编辑技术与应用

Yuan Chen
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引用次数: 3

摘要

基因编辑是一种基因工程,在生物体的基因组中插入、删除、修改或替换DNA。与将遗传物质随机插入宿主基因组的传统方法不同,当前的基因编辑技术瞄准并改变特定的基因组位置。锌指核酸酶(ZFNs)、转录激活因子样效应物核酸酶(TALENs)和聚集规律间隔短回传重复序列(crispr)/Cas9核酸酶系统是三种常见的基因编辑技术。这些技术已广泛应用于基因组工程中,通过诱导DNA断裂刺激容易出错的修复,如同源重组(HR)或非同源末端连接(NHEJ),从而实现大范围的突变。它们成功地使特定基因组位点的特定编辑、修改和操作成为可能(表1)[1]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Introductory Chapter: Gene Editing Technologies and Applications
Gene editing is a type of genetic engineering in which DNA is inserted, deleted, modified, or replaced in the genome of a living organism. Unlike traditional methods that randomly insert genetic material into a host genome, current gene editing technologies target and change the specific genome locations. Zinc finger nucleases (ZFNs), transcription activator-like effectors nucleases (TALENs), and clustered regularly interspaced short palindromic repeats (CRISPRs)/Cas9 nuclease system are the three common gene editing technologies. These technologies have been widely used in genome engineering to enable a broad range of mutation by inducing DNA breaks that stimulate error-prone repairs such as homologous recombination (HR) or nonhomologous end joining (NHEJ). They successfully make it possible to achieve site-specific editing, modification, and manipulation at specific genomic sites (Table 1) [1].
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