清脆的
生物
Cas9
基因组编辑
核酸内切酶
遗传学
基因
引导RNA
回文
艾美球虫
计算生物学
DNA
作者
Xinming Tang,Jingxia Suo,Lin Liang,Chunhui Duan,Dandan Hu,Xiaolong Gu,Yonglan Yu,Xianyong Liu,Shangjin Cui,Xun Suo
标识
DOI:10.1186/s13567-020-00766-0
摘要
Eimeria tenella has emerged as valuable model organism for studying the biology and immunology of protozoan parasites with the establishment of the reverse genetic manipulation platform. In this report, we described the application of CRISPR (clustered regularly interspaced short palindromic repeat)/Cas9 (endonuclease) system for efficient genetic editing in E. tenella, and showed that the CRISPR/Cas9 system mediates site-specific double-strand DNA breaks with a single guide RNA. Using this system, we successfully tagged the endogenous microneme protein 2 (EtMic2) by inserting the red fluorescent protein into the C-terminal of EtMic2. Our results extended the utility of the CRISPR/Cas9-mediated genetic modification system to E. tenella, and opened a new avenue for targeted investigation of gene functions in apicomplexan parasites.
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