CRISPR-Cas9 tools have revolutionized genetic engineering, yet the efficient precise integration of DNA cargos, particularly for large DNA payloads (>1 kilobase, kb), remains a technical bottleneck. Herein, we develop a Recombinases (Redα/β)-enhanced DNA integration-CRISPR-Cas9 approach, referred to as RED-CRISPR, which offers a versatile yet robust homology-directed repair (HDR) strategy enabling efficient and precise kb-scale DNA insertion across various cell types, including immortalized and primary cells of variable origins. RED-CRISPR significantly enhances HDR efficiencies by 2- to 5-fold change across diverse loci and further elevates HDR rates by 1.5- to 2.5-fold when synergizing with other HDR-enhancing strategies. We achieved up to 45% knock-in efficiency for CAR-T cell manufacturing, and attained 43% knock-in rate for generation of genetically modified mice using an 8-kb DNA cargo. Through a head-to-head comparison, RED-CRISPR profoundly mitigates off-target mutational burden and chromosomal translocations. We envision RED-CRISPR as a powerful genome-editing tool with broad biomedical and therapeutic applications.
Efficient high-precision transgene knock-in by Recombinases (Redα/β)-enhanced DNA integration-CRISPR-Cas9 (RED-CRISPR).
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作者:Li Wenqing, Liu Senquan, Fang Xiaoyu, Zou Jiaqi, Jiang Qin, Min Xiaolin, Zhu Xiaoli, Cao Yuzhu, Gao Xiaoxiao, Han Wenjie, Azhar Muhammad, Xing Xuemei, Li Fudong, Zhang Youming, Liu Hongbin, Cheng Linzhao, Wang Chengkun, Bao Jianqiang
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2025 | 起止号: | 2025 Dec 10; 17(1):538 |
| doi: | 10.1038/s41467-025-67239-w | ||
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