Yao Bing, Yang Qiangbing, Snijders Blok Christian J B, Daniels Mark A, Doevendans Pieter A, Schiffelers Raymond, Sluijter Joost P G, Lei Zhiyong
Experimental Cardiology Laboratory, Department of Cardiology, Division of Heart and Lungs, University Medical Center Utrecht, the Netherlands.
Regenerative Medicine Center Utrecht, Circulatory Health Research Center, University Medical Center Utrecht, University Utrecht, the Netherlands.
FEBS Lett. 2025 Sep;599(17):2543-2554. doi: 10.1002/1873-3468.70097. Epub 2025 Jun 24.
Prime editing (PE) represents a transformative genome-editing technology and enables precise insertions, deletions, and base substitutions without introducing double-strand breaks, thereby reducing undesired indels and off-target effects. Despite advancements in enhanced prime editors and optimized prime editing guide RNAs (pegRNAs), designing effective pegRNAs remains a major challenge. The phospholamban (PLN) R14del mutation is associated with cardiomyopathies, making it a crucial target for precise gene-editing strategies. In this study, we explored pegRNA features that contribute to high editing efficiency using the FluoPEER.PLN R14del reporter cell line. Through systematic screening, we identified three pegRNAs with significantly enhanced editing efficiency. Our findings underscore the importance of pegRNA secondary structure and stability in optimizing prime editing, providing valuable insights into precise gene correction strategies.
碱基编辑(PE)是一种变革性的基因组编辑技术,能够实现精确的插入、缺失和碱基替换,而无需引入双链断裂,从而减少不必要的插入缺失和脱靶效应。尽管增强型碱基编辑器和优化的碱基编辑引导RNA(pegRNA)取得了进展,但设计有效的pegRNA仍然是一项重大挑战。磷酸受纳蛋白(PLN)R14del突变与心肌病相关,使其成为精确基因编辑策略的关键靶点。在本研究中,我们使用FluoPEER.PLN R14del报告细胞系探索了有助于提高编辑效率的pegRNA特征。通过系统筛选,我们鉴定出三种编辑效率显著提高的pegRNA。我们的研究结果强调了pegRNA二级结构和稳定性在优化碱基编辑中的重要性,为精确基因校正策略提供了有价值的见解。