Engineered <scp>CRISPR RNA</scp> improves the <scp>RNA</scp> cleavage efficiency of <scp>hfCas13X</scp>
As the most compact variant in the Cas13 family, CRISPR-Cas13X holds considerable promise for gene therapy applications. The development of high-fidelity Cas13X (hfCas13X) mutants has enhanced the safety profile for in vivo applications. However, a notable reduction in on-target cleavage efficiency accompanies the diminished collateral cleavage activity in hfCas13X. In this study, we obtained two engineered crRNA mutants that notably enhance the on-target cleavage efficiency of hfCas13X. Furthermore, we have identified a novel crRNA structure that consistently augments the on-target cleavage efficiency of hfCas13X across various cellular environments, without significant enhancement of its collateral activity. These findings collectively enrich the gene-editing toolkit, presenting a more effective hfCas13X system for future research and application.
Authors
- Yimu Yang (ORCID: https://orcid.org/0000-0003-3674-3984)
- Pingping Shangguan
- Wenxia Zhang (ORCID: https://orcid.org/0000-0003-2280-5734)
- Zehui Liu (ORCID: https://orcid.org/0000-0002-7356-876X)
- Xi Mao (ORCID: https://orcid.org/0000-0001-8047-0421)
- Zhang Qi (ORCID: https://orcid.org/0000-0003-2868-1816)
- Yingle Liu
- Tong Pan
- Yi Zhang (ORCID: https://orcid.org/0000-0002-9418-2428)
- Haili Wang
Institutions
- Wuhan University (CN)
- State Key Laboratory of Virology
Publication Details
- Journal
- FEBS Letters
- Published
- 2024-09-26
- DOI
- https://doi.org/10.1002/1873-3468.15025
- Citations
- 1
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.23
Funders
- National Key Research and Development Program of China