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Large chromosomal segment deletions by CRISPR/LbCpf1-mediated multiplex gene editing in soybean

J Integr Plant Biol. 2021-09; 
Kaixuan Duan, Yuanyuan Cheng, Jing Ji, Chenchen Wang, Yongshu Wei, Yuanchao Wang
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Plasmid DNA Preparation … The coding sequence of LbCpf1 plus 5′ nuclear localization sequence and 3×FLAG was synthesized by Genscript (Nanjing, China) and cloned into the pFGC5941 plasmid through XhoI/BamHI double digestion. The soybean ubiquitin and CaMV 35S promoters and the … Get A Quote

摘要

The creation of new soybean varieties has been limited by genomic duplication and redundancy. Efficient multiplex gene editing and large chromosomal segment deletion through clustered regularly interspaced palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) systems are promising strategies for overcoming these obstacles. CRISPR/Cpf1 is a robust tool for multiplex gene editing. However, large chromosomal excision mediated by CRISPR/Cpf1 has been reported in only a few non-plant species. Here, we report on CRISPR/LbCpf1-induced large chromosomal segment deletions in soybean using multiplex gene targeting. The CRISPR/LbCpf1 system was optimized for direct repeat and guide RNA lengths in crispr RNA (crRNA)... More

关键词

CRISPR/LbCpf1, chromosomal segment deletion, multiplex gene editing, soybean