清脆的
基因组编辑
Cas9
多粘菌拟杆菌
生物
计算生物学
基因组
多路复用
遗传学
亚基因组mRNA
回文
点突变
基因
突变
细菌
作者
Giulia Ravagnan,Meliawati Meliawati,Jochen Schmid
出处
期刊:Methods in molecular biology
日期:2024-01-01
卷期号:: 267-280
标识
DOI:10.1007/978-1-0716-3658-9_16
摘要
In recent years, the clustered regularly interspaced palindromic repeats-Cas (CRISPR-Cas) technology has become the method of choice for precision genome editing in many organisms due to its simplicity and efficacy. Multiplex genome editing, point mutations, and large genomic modifications are attractive features of the CRISPR-Cas9 system. These applications facilitate both the ease and velocity of genetic manipulations and the discovery of novel functions. In this protocol chapter, we describe the use of a CRISPR-Cas9 system for multiplex integration and deletion modifications, and deletions of large genomic regions by the use of a single guide RNA (sgRNA), and, finally, targeted point mutation modifications in Paenibacillus polymyxa.
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