CSpace  > 生态毒理学研究中心
Knock-In Strategy for Editing Human and Zebrafish Mitochondrial DNA Using Mito-CRISPR/Cas9 System
Bian, Wan-Ping; Chen, Yan-Ling; Luo, Juan-Juan; Wang, Chao; Xie, Shao-Lin; Pei, De-Sheng
2019-04-01
摘要The mitochondria DNA (mtDNA) editing tool, zinc finger nucleases (ZFNs), transcription activator-like effector nuclease (TALENs), and clustered regularly interspaced short palindromic repeats/CRISPR associated protein 9 (CRISPR/Cas9) system, is a promising approach for the treatment of mtDNA diseases by eliminating mutant mitochondrial genomes. However, there have been no reports of repairing the mutant mtDNA with homologous recombination strategy to date. Here, we show a mito-CRISPR/Cas9 system that mito-Cas9 protein can specifically target mtDNA and reduce mtDNA copy number in both human cells and zebrafish. An exogenous single-stranded DNA with short homologous arm was knocked into the targeting loci accurately, and this mutagenesis could be steadily transmitted to F-1 generation of zebrafish. Moreover, we found some major factors involved in nuclear DNA repair were upregulated significantly by the mito-CRISPR/Cas9 system. Taken together, our data suggested that the mito-CRISPR/Cas9 system could be a useful method to edit mtDNA by knock-in strategy, providing a potential therapy for the treatment of inherited mitochondrial diseases.
关键词mito-CRISPR/Cas9 mitochondria mtDNA editing ssDNA zebrafish
DOI10.1021/acssynbio.8b00411
发表期刊ACS SYNTHETIC BIOLOGY
ISSN2161-5063
卷号8期号:4页码:621-632
收录类别SCI
WOS记录号WOS:000465487100002
语种英语