Yue Jin-Jun, Yuan Jin-Ling, Wu Fu-Hui, Yuan Yu-Hsuan, Cheng Qiao-Wei, Hsu Chen-Tran, Lin Choun-Sea
Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Hangzhou, China.
Agricultural Biotechnology Research Center, Academia Sinica, Taipei, Taiwan.
Front Genome Ed. 2021 Aug 11;3:717017. doi: 10.3389/fgeed.2021.717017. eCollection 2021.
In the clustered regulatory interspaced short palindromic repeats (CRISPR)/CRISPR associated protein (Cas) system, protoplasts are not only useful for rapidly validating the mutagenesis efficiency of various RNA-guided endonucleases, promoters, sgRNA designs, or Cas proteins, but can also be a platform for DNA-free gene editing. To date, the latter approach has been applied to numerous crops, particularly those with complex genomes, a long juvenile period, a tendency for heterosis, and/or self-incompatibility. Protoplast regeneration is thus a key step in DNA-free gene editing. In this report, we review the history and some future prospects for protoplast technology, including protoplast transfection, transformation, fusion, regeneration, and current protoplast applications in CRISPR/Cas-based breeding.
在成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白(Cas)系统中,原生质体不仅有助于快速验证各种RNA引导的核酸内切酶、启动子、sgRNA设计或Cas蛋白的诱变效率,还可作为无DNA基因编辑的平台。迄今为止,后一种方法已应用于多种作物,特别是那些基因组复杂、幼年期长、具有杂种优势倾向和/或自交不亲和性的作物。因此,原生质体再生是无DNA基因编辑的关键步骤。在本报告中,我们回顾了原生质体技术的历史和一些未来前景,包括原生质体转染、转化、融合、再生以及目前原生质体在基于CRISPR/Cas的育种中的应用。