Next-generation CRISPR technology for genome, epigenome and mitochondrial editing

被引:5
|
作者
Lau, Cia-Hin [1 ]
Liang, Qing-Le [2 ]
Zhu, Haibao [1 ]
机构
[1] Shantou Univ, Coll Sci, Dept Biol, Shantou 515063, Guangdong, Peoples R China
[2] Chongqing Univ, Jiangjin Hosp, Dept Clin, Lab Med, Chongqing, Peoples R China
关键词
Base editor; CRISPR; Epigenome editing; Genome editing; Integrase; Mitochondrial editing; Prime editor; Transposase; HOMOLOGY-DIRECTED-REPAIR; RNA-GUIDED ENDONUCLEASE; TARGET DNA RECOGNITION; PLURIPOTENT STEM-CELLS; STRUCTURAL BASIS; BASE EDITOR; OFF-TARGET; SELECTIVE DEGRADATION; HUMAN FIBROBLASTS; CLINICAL-TRIALS;
D O I
10.1007/s11248-024-00404-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The application of rapidly growing CRISPR toolboxes and methods has great potential to transform biomedical research. Here, we provide a snapshot of up-to-date CRISPR toolboxes, then critically discuss the promises and hurdles associated with CRISPR-based nuclear genome editing, epigenome editing, and mitochondrial editing. The technical challenges and key solutions to realize epigenome editing in vivo, in vivo base editing and prime editing, mitochondrial editing in complex tissues and animals, and CRISPR-associated transposases and integrases in targeted genomic integration of very large DNA payloads are discussed. Lastly, we discuss the latest situation of the CRISPR/Cas9 clinical trials and provide perspectives on CRISPR-based gene therapy. Apart from technical shortcomings, ethical and societal considerations for CRISPR applications in human therapeutics and research are extensively highlighted.
引用
收藏
页码:323 / 357
页数:35
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