| Literature DB >> 29910177 |
Huihui Sun1, Fanfan Li2, Jie Liu2, Fayu Yang1, Zhenhai Zeng1, Xiujuan Lv1, Mengjun Tu1, Yeqing Liu1, Xianglian Ge1, Changbao Liu2, Junzhao Zhao2, Zongduan Zhang1, Jia Qu1, Zongming Song3, Feng Gu4.
Abstract
Cpf1 has been harnessed as a tool for genome manipulation in various species because of its simplicity and high efficiency. Our recent study demonstrated that FnCpf1 could be utilized for human genome editing with notable advantages for target sequence selection due to the flexibility of the protospacer adjacent motif (PAM) sequence. Multiplex genome editing provides a powerful tool for targeting members of multigene families, dissecting gene networks, modeling multigenic disorders in vivo, and applying gene therapy. However, there are no reports at present that show FnCpf1-mediated multiplex genome editing via a single customized CRISPR RNA (crRNA) array. In the present study, we utilize a single customized crRNA array to simultaneously target multiple genes in human cells. In addition, we also demonstrate that a single customized crRNA array to target multiple sites in one gene could be achieved. Collectively, FnCpf1, a powerful genome-editing tool for multiple genomic targets, can be harnessed for effective manipulation of the human genome.Entities:
Keywords: FnCpf1; crRNA; multiplex genome editing
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Year: 2018 PMID: 29910177 PMCID: PMC6094396 DOI: 10.1016/j.ymthe.2018.05.021
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454