Cheng Yiqiu, Zhang Lei, Li Jing, Dang Xiaofei, Zhu Jian-Kang, Shimada Hiroaki, Miki Daisuke
Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.
University of Chinese Academy of Sciences, Beijing, China.
Front Plant Sci. 2024 Mar 13;15:1360925. doi: 10.3389/fpls.2024.1360925. eCollection 2024.
Gene targeting (GT) is a promising tool for precise manipulation of genome sequences, however, GT in seed plants remains a challenging task. The simple and direct way to improve the efficiency of GT via homology-directed repair (HDR) is to increase the frequency of double-strand breaks (DSBs) at target sites in plants. Here we report an all-in-one approach of GT in Arabidopsis by combining a transcriptional and a translational enhancer for the Cas expression. We find that facilitating the expression of Cas9 and Cas12a variant by using enhancers can improve DSB and subsequent knock-in efficiency in the Arabidopsis genome. These results indicate that simply increasing Cas protein expression at specific timings - egg cells and early embryos - can improve the establishment of heritable GTs. This simple approach allows for routine genome engineering in plants.
基因靶向(GT)是一种用于精确操纵基因组序列的有前景的工具,然而,种子植物中的基因靶向仍然是一项具有挑战性的任务。通过同源定向修复(HDR)提高基因靶向效率的简单直接方法是增加植物靶位点双链断裂(DSB)的频率。在这里,我们报告了一种在拟南芥中进行基因靶向的一体化方法,该方法通过组合用于Cas表达的转录增强子和翻译增强子来实现。我们发现,使用增强子促进Cas9和Cas12a变体的表达可以提高拟南芥基因组中的双链断裂及随后的敲入效率。这些结果表明,仅在特定时期——卵细胞和早期胚胎——增加Cas蛋白表达就可以提高可遗传基因靶向的成功率。这种简单的方法使得植物中的常规基因组工程成为可能。