Evolution of CRISPR/Cas Systems for Precise Genome Editing

被引:12
|
作者
Hryhorowicz, Magdalena [1 ]
Lipinski, Daniel [1 ]
Zeyland, Joanna [1 ]
机构
[1] Poznan Univ Life Sci, Dept Biochem & Biotechnol, Dojazd 11, PL-60632 Poznan, Poland
关键词
CRISPR/Cas9; system; CRISPR classification; Cas9; nuclease; Cas12a nuclease; Cas13a nuclease; genome editing; base editors; prime editors; CRISPR-CAS9; NUCLEASES; STRUCTURAL BASIS; IMMUNE-SYSTEM; STEM-CELLS; DNA; CAS9; BASE; GENE; ENDONUCLEASE; SPECIFICITY;
D O I
10.3390/ijms241814233
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bacteria-derived CRISPR/Cas (an acronym for regularly interspaced short palindromic repeats/CRISPR-associated protein) system is currently the most widely used, versatile, and convenient tool for genome engineering. CRISPR/Cas-based technologies have been applied to disease modeling, gene therapies, transcriptional modulation, and diagnostics. Nevertheless, some challenges remain, such as the risk of immunological reactions or off-target effects. To overcome these problems, many new methods and CRISPR/Cas-based tools have been developed. In this review, we describe the current classification of CRISPR systems and new precise genome-editing technologies, summarize the latest applications of this technique in several fields of research, and, finally, discuss CRISPR/Cas system limitations, ethical issues, and challenges.
引用
收藏
页数:15
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