State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.
Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, China.
Nat Chem Biol. 2022 Jan;18(1):29-37. doi: 10.1038/s41589-021-00889-1. Epub 2021 Oct 28.
The recently reported prime editor (PE) can produce all types of base substitution, insertion and deletion, greatly expanding the scope of genome editing. However, improving the editing efficiency and precision of PE represents a major challenge. Here, we report an approach termed the homologous 3' extension mediated prime editor (HOPE). HOPE uses paired prime editing guide RNAs (pegRNAs) encoding the same edits in both sense and antisense DNA strands to achieve high editing efficiency in human embryonic kidney 293T cells as well as mismatch repair-deficient human colorectal carcinoma 116 cells. In addition, we found that HOPE shows greatly improved product purity compared to the original PE3 system. We envision that this enhanced tool could broaden both fundamental research and therapeutic applications of prime editing.
最近报道的 Prime Editor(PE)可以产生所有类型的碱基替换、插入和缺失,极大地扩展了基因组编辑的范围。然而,提高 PE 的编辑效率和精度是一个主要挑战。在这里,我们报告了一种称为同源 3' 延伸介导的 Prime Editor(HOPE)的方法。HOPE 使用配对的 Prime Editing 向导 RNA(pegRNA)在 sense 和 antisense DNA 链上编码相同的编辑,以在人胚肾 293T 细胞以及错配修复缺陷的人结直肠癌细胞 116 中实现高效率的编辑。此外,我们发现 HOPE 与原始的 PE3 系统相比,显示出大大提高的产物纯度。我们设想这个增强的工具可以拓宽 Prime Editing 的基础研究和治疗应用。