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一直在不断进步——基于CRISPR/Cas的植物基因组工程工具开发的最新进展

Getting better all the time - recent progress in the development of CRISPR/Cas-based tools for plant genome engineering.

作者信息

Capdeville Niklas, Schindele Patrick, Puchta Holger

机构信息

Karlsruhe Institute of Technology (KIT), Botanical Institute, Chair Molecular Biology and Biochemistry, Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.

Karlsruhe Institute of Technology (KIT), Botanical Institute, Chair Molecular Biology and Biochemistry, Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.

出版信息

Curr Opin Biotechnol. 2023 Feb;79:102854. doi: 10.1016/j.copbio.2022.102854. Epub 2022 Nov 28.

Abstract

Since their first adaptation for plant genome editing, clustered regularly interspaced short palindromic repeats/CRISPR-associated system nucleases and tools have revolutionized the field. While early approaches focused on targeted mutagenesis that relies on mutagenic repair of induced double-strand breaks, newly developed tools now enable the precise induction of predefined modifications. Constant efforts to optimize these tools have led to the generation of more efficient base editors with enlarged editing windows and have enabled previously unachievable C-G transversions. Prime editors were also optimized for the application in plants and now allow to accurately induce substitutions, insertions, and deletions. Recently, great progress was made through precise restructuring of chromosomes, which enables not only the breakage or formation of genetic linkages but also the swapping of promoters.

摘要

自从成簇规律间隔短回文重复序列/CRISPR相关系统核酸酶及工具首次应用于植物基因组编辑以来,该领域发生了革命性变化。早期方法侧重于依赖诱导双链断裂的诱变修复进行靶向诱变,而新开发的工具现在能够精确诱导预定义的修饰。不断优化这些工具的努力已产生了具有更大编辑窗口的更高效碱基编辑器,并实现了以前无法实现的C-G颠换。引导编辑器也针对植物应用进行了优化,现在可以精确诱导替换、插入和缺失。最近,通过染色体的精确重组取得了巨大进展,这不仅能够实现遗传连锁的断裂或形成,还能实现启动子的交换。

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