Genome editing in nonhuman primates: approach to generating human disease models

被引:44
作者
Chen, Y. [1 ,2 ]
Niu, Y. [1 ,2 ]
Ji, W. [1 ,2 ]
机构
[1] Kunming Univ Sci & Technol, Yunnan Key Lab Primate Biomed Res, Inst Primate Translat Med, Kunming, Yunnan, Peoples R China
[2] Natl Engn Res Ctr Biomed & Anim Sci, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
CRISPR; Cas9; disease model; genome editing; nonhuman primate; TALENs; ZINC-FINGER NUCLEASES; ONE-STEP GENERATION; CYNOMOLGUS MONKEY; GENE MODIFICATIONS; TALEN; MICE; RHESUS; DNA; CRISPR-CAS9; MUTAGENESIS;
D O I
10.1111/joim.12469
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Nonhuman primates (NHPs) are superior than rodents to be animal models for the study of human diseases, due to their similarities in terms of genetics, physiology, developmental biology, social behaviour and cognition. Transgenic animals have become a key tool in functional genomics to generate models for human diseases and validate new drugs. However, until now, progress in the field of transgenic NHPs has been slow because of technological limitations. Many human diseases, including neurodegenerative disorders, are caused by mutations in endogenous genes. Fortunately, recent developments in precision gene editing have led to the generation of NHP models for human diseases. Since 2014, there have been several reports of the generation of monkey models using transcription activator-like endonucleases (TALENs) or clustered regularly interspaced short palindromic repeats (CRISPR/Cas9); some of these NHP models showed symptoms that were much closer to those of human diseases than have been seen previously in mouse models. No off-targeting was observed in the NHP models, and multiple gene knockout and biallelic mutants were feasible with low efficiency. These findings suggest that there are many possibilities to establish NHP models for human diseases that can mimic human diseases more faithfully than rodent models.
引用
收藏
页码:246 / 251
页数:6
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