CRISPR/Cas9 ribonucleoprotein mediated DNA-free genome editing in larch.

Forestry research Pub Date : 2024-10-31 eCollection Date: 2024-01-01 DOI:10.48130/forres-0024-0033
Miaomiao Ma, Chan Zhang, Lijing Yu, Jingli Yang, Chenghao Li
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Abstract

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 via 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 in vitro. 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.

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落叶松中 CRISPR/Cas9 核糖核蛋白介导的无 DNA 基因组编辑。
本文介绍了一种通过粒子轰击传递 CRISPR/Cas9 核糖核蛋白复合物(RNPs)的落叶松无 DNA 基因编辑方法。详细过程包括通过粒子轰击建立转基因系统以转化胚胎性胼胝体、验证 RNPs 的功能、优化包被和递送技术、促进体细胞胚胎成熟、再生小植株以及精确鉴定突变体。确定的最佳粒子轰击参数为 1,100 psi 和 9 cm 的距离,并在体外验证了靶标的编辑效率。随后,RNPs 被转移到胚胎性胼胝体中。在靶标 1 和靶标 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%。适用于落叶松的无 DNA 粒子轰击转化方法已经建立。本研究表明,无 DNA 编辑技术已成功应用于落叶松。该方法可实现落叶松基因组的定向基因组编辑,避免了传统转基因方法的基因组整合风险和漫长的育种周期。此外,它还可广泛应用于生产基因组编辑的针叶植物,并有望实现商业化。
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Characterization of UGT71, a major glycosyltransferase family for triterpenoids, flavonoids and phytohormones-biosynthetic in plants. CRISPR/Cas9 ribonucleoprotein mediated DNA-free genome editing in larch. The revelation of genomic breed composition using target capture sequencing: a case of Taxodium. Responses of isolated balsam-fir stem segments to exogenous ACC, IAA, and IBA. Combating browning: mechanisms and management strategies in in vitro culture of economic woody plants.
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