The Key Laboratory of Plant Development and Environmental Adaptation Biology, Ministry of Education, School of Life Sciences, Shandong University, Qingdao, Shandong, China.
National Key Laboratory of Wheat Improvement, Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agriculture Sciences in Weifang, Weifang, Shandong, China.
Genome Biol. 2024 Aug 9;25(1):215. doi: 10.1186/s13059-024-03358-9.
Base editing is a powerful tool for artificial evolution to create allelic diversity and improve agronomic traits. However, the great evolutionary potential for every sgRNA target has been overlooked. And there is currently no high-throughput method for generating and characterizing as many changes in a single target as possible based on large mutant pools to permit rapid gene directed evolution in plants.
In this study, we establish an efficient germline-specific evolution system to screen beneficial alleles in Arabidopsis which could be applied for crop improvement. This system is based on a strong egg cell-specific cytosine base editor and the large seed production of Arabidopsis, which enables each T1 plant with unedited wild type alleles to produce thousands of independent T2 mutant lines. It has the ability of creating a wide range of mutant lines, including those containing atypical base substitutions, and as well providing a space- and labor-saving way to store and screen the resulting mutant libraries. Using this system, we efficiently generate herbicide-resistant EPSPS, ALS, and HPPD variants that could be used in crop breeding.
Here, we demonstrate the significant potential of base editing-mediated artificial evolution for each sgRNA target and devised an efficient system for conducting deep evolution to harness this potential.
碱基编辑是一种强大的人工进化工具,可用于创造等位基因多样性和改良农艺性状。然而,每个 sgRNA 靶标都具有巨大的进化潜力,这一点被忽视了。目前,还没有基于大型突变体库生成和表征尽可能多的单个靶标变化的高通量方法,从而无法在植物中实现快速的基因定向进化。
在这项研究中,我们建立了一个有效的生殖系特异性进化系统,用于筛选拟南芥中的有益等位基因,这可应用于作物改良。该系统基于强的卵母细胞特异性胞嘧啶碱基编辑器和拟南芥的大量种子生产,使每个具有未编辑野生型等位基因的 T1 植物能够产生数千个独立的 T2 突变系。它具有创建广泛的突变系的能力,包括那些含有非典型碱基取代的突变系,并且为存储和筛选产生的突变文库提供了节省空间和劳力的方法。利用该系统,我们高效地生成了可用于作物育种的除草剂抗性 EPSPS、ALS 和 HPPD 变体。
在这里,我们展示了碱基编辑介导的人工进化在每个 sgRNA 靶标中的巨大潜力,并设计了一种有效的系统来进行深入进化以利用这种潜力。