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A Single Multiplex crRNA Array for FnCpf1-Mediated Human Genome Editing.


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.

SUBMITTER: Sun H 

PROVIDER: S-EPMC6094396 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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A Single Multiplex crRNA Array for FnCpf1-Mediated Human Genome Editing.

Sun Huihui H   Sun Huihui H   Li Fanfan F   Liu Jie J   Yang Fayu F   Zeng Zhenhai Z   Lv Xiujuan X   Tu Mengjun M   Liu Yeqing Y   Ge Xianglian X   Liu Changbao C   Zhao Junzhao J   Zhang Zongduan Z   Qu Jia J   Song Zongming Z   Gu Feng F   Gu Feng F  

Molecular therapy : the journal of the American Society of Gene Therapy 20180615 8


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  ...[more]

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