CRISPR-Cas9作为分子瑞士军刀的工程进展

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS Synthetic biology (Oxford, England) Pub Date : 2020-10-24 eCollection Date: 2020-01-01 DOI:10.1093/synbio/ysaa021
Grace A Meaker, Emma J Hair, Thomas E Gorochowski
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引用次数: 8

摘要

rna引导的内切酶系统CRISPR-Cas9自发现以来已被广泛修改,使其能力远远超出双链切割,可以实现高保真的插入、删除和单碱基编辑。由于CRISPR-Cas9的模块化结构以及其组成部分对修改和新功能元素融合的稳健性,这些创新成为可能。在这里,我们回顾了目前可用于各种基因组编辑任务的基于crispr - cas9的系统的广泛工具包。我们提供了他们的核心分子结构和机制的概述和提炼的设计原则,用于工程其不同的功能。最后,我们将超越生物化学,着眼于这些CRISPR-Cas9系统所面临的社会和伦理挑战,如果它们的变革能力要以安全和可接受的方式部署。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife.

The RNA-guided endonuclease system CRISPR-Cas9 has been extensively modified since its discovery, allowing its capabilities to extend far beyond double-stranded cleavage to high fidelity insertions, deletions and single base edits. Such innovations have been possible due to the modular architecture of CRISPR-Cas9 and the robustness of its component parts to modifications and the fusion of new functional elements. Here, we review the broad toolkit of CRISPR-Cas9-based systems now available for diverse genome-editing tasks. We provide an overview of their core molecular structure and mechanism and distil the design principles used to engineer their diverse functionalities. We end by looking beyond the biochemistry and toward the societal and ethical challenges that these CRISPR-Cas9 systems face if their transformative capabilities are to be deployed in a safe and acceptable manner.

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