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Fusions of Catalytically Inactive RusA to FokI Nuclease Coupled with PNA Enable Programmable Site-Specific Double-Stranded DNA Breaks

Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Programmable site-specific nucleases have revolutionized genome editing. However, these systems still face challenges such as guide dependency, delivery issues, and off-target effects. Harnessing the natural functions of structure-guided nucleases offers promising alternatives for generating site-specific double-stranded DNA breaks. Yet, structure-guided nucleases require precise reaction conditions and validation for in vivo applicability. To address these limitations, we developed the P NA- c oupled F ok I -(d) R us A ( PC-FIRA ) system. PC-FIRA combines the sequence-specific binding ability of peptide nucleic acids (PNAs) with the catalytic efficiency of FokI nuclease fused to a structurally guided inactive RusA resolvase (FokI-(d)RusA). This system allows for precise double-stranded DNA breaks without the constraints of existing site-specific nuclease and structure-guided nucleases. Through in vitro optimizations, we achieved high target specificity and cleavage efficiency. This included adjusting the incubation temperature, buffer composition, ion concentration, and cleavage timing. Diverse DNA structures, such as Holliday junctions and linear and circular DNA, were tested, demonstrating the potential activity on different target forms. Further investigation has revealed the PC-FIRA system’s capacity for facilitating the precise deletion of large DNA fragments. This can be useful in cloning, large-fragment DNA assembly, and genome engineering, with promising applications in biotechnology, medicine, agriculture, and synthetic biology.
Source: ACS Omega
DOI: 10.1021/acsomega.4c11282
Language: English
Open Access status: gold
Estimated APC paid: $1,935
OpenAlex ID: W4410352197
FWCI:
Cites: 37
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Related to: 10