Development and expansion of the CRISPR/Cas9 toolboxes for powerful genome engineering in yeast

被引:9
作者
Cai, Guang [1 ]
Lin, Zhenquan [1 ]
Shi, Shuobo [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
关键词
CRISPR; Cas9; Yeast; Synthetic Biology; Multiplex Genetic editing; Effector protein; RNA-POLYMERASE-III; SACCHAROMYCES-CEREVISIAE; IN-VIVO; CRISPR-CAS9; NUCLEASES; WEB TOOL; CAS9; DNA; INTEGRATION; STEP; RECOMBINATION;
D O I
10.1016/j.enzmictec.2022.110056
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Yeasts represent a group of the microorganisms most frequently seen in biotechnology. Recently, the class 2 type II CRISPR system (CRISPR/Cas9) has become the principal toolbox for genome editing. By efficiently implementing genetic manipulations such as gene integration/knockout, base editor, and transcription regulation, the development of biotechnological applications in yeasts has been extensively promoted. The genome-level tools based on CRISPR/Cas9, used for screening and identifying functional genes/gene clusters, are also advancing. In general, CRISPR/Cas9-assisted editing tools have gradually become standardized and function as host-orthogonal genetic systems, which results in time-saving for strain engineering and biotechnological application processes. In this review, we summarize the key points of the basic elements in the CRISPR/Cas9 system, including Cas9 variants, guide RNA, donors, and effectors. With a focus on yeast, we have also introduced the development of various CRISPR/Cas9 systems and discussed their future possibilities.
引用
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页数:10
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