Ma Miaomiao, Zhang Chan, Yu Lijing, Yang Jingli, Li Chenghao
State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, China.
For Res (Fayettev). 2024 Oct 31;4:e036. doi: 10.48130/forres-0024-0033. eCollection 2024.
Here, a DNA-free genetic editing approach is presented for larch by delivering ribonucleoprotein complexes (RNPs) of CRISPR/Cas9 through particle bombardment. The detailed procedure encompasses creating a transgenic system particle bombardment for the transformation of embryogenic callus, validating the functionality of RNPs, optimizing coating and delivery techniques, enhancing somatic embryo maturation, regenerating plantlets, and precisely identifying mutants. The optimal particle bombardment parameters were determined at 1,100 psi and a distance of 9 cm and the editing efficiency of the targets was verified . Subsequently, the RNPs were transferred into the embryogenic callus. Mutant plants were obtained in targets 1 and target 2. The efficiencies of obtaining albino somatic embryos were 1.423% and 2.136%, respectively. A DNA-free particle bombardment transformation method suitable for larch has been established. The present study demonstrates that the DNA-free editing technology has been successfully implemented in larch. This method can achieve targeted genome editing in the larch genome, avoiding the risks of genomic integration and the lengthy breeding cycles associated with traditional transgenic methods. Moreover, it may be widely applicable for producing genome-edited conifer plants and holds great promise for commercialization.
本文介绍了一种通过粒子轰击递送CRISPR/Cas9核糖核蛋白复合物(RNP)对落叶松进行无DNA基因编辑的方法。详细步骤包括创建一个转基因系统——通过粒子轰击转化胚性愈伤组织、验证RNP的功能、优化包被和递送技术、促进体细胞胚成熟、再生小植株以及精确鉴定突变体。确定了最佳粒子轰击参数为1100磅力/平方英寸和9厘米的距离,并验证了靶点的编辑效率。随后,将RNP转入胚性愈伤组织。在靶点1和靶点2中获得了突变植株。获得白化体细胞胚的效率分别为1.423%和2.136%。建立了一种适用于落叶松的无DNA粒子轰击转化方法。本研究表明,无DNA编辑技术已在落叶松中成功实施。该方法可在落叶松基因组中实现靶向基因组编辑,避免了基因组整合风险以及与传统转基因方法相关的漫长育种周期。此外,它可能广泛适用于生产基因组编辑的针叶树植物,并具有很大的商业化潜力。