Department of Gynecological oncology, the First Affiliated Hospital, Sun Yat-sen University, Zhongshan 2nd Road, Yuexiu, Guangzhou, 510080, Guangdong, China.
Center for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, Guangdong, China.
Nat Commun. 2022 Mar 17;13(1):1425. doi: 10.1038/s41467-022-29089-8.
Genome editing technologies hold tremendous potential in biomedical research and drug development. Therefore, it is imperative to discover gene editing tools with superior cutting efficiency, good fidelity, and fewer genomic restrictions. Here, we report a CRISPR/Cas9 from Faecalibaculum rodentium, which is characterized by a simple PAM (5'-NNTA-3') and a guide RNA length of 21-22 bp. We find that FrCas9 could achieve comparable efficiency and specificity to SpCas9. Interestingly, the PAM of FrCas9 presents a palindromic sequence, which greatly expands its targeting scope. Due to the PAM sequence, FrCas9 possesses double editing-windows for base editor and could directly target the TATA-box in eukaryotic promoters for TATA-box related diseases. Together, our results broaden the understanding of CRISPR/Cas-mediated genome engineering and establish FrCas9 as a safe and efficient platform for wide applications in research, biotechnology and therapeutics.
基因组编辑技术在生物医学研究和药物开发中具有巨大的潜力。因此,发现具有更高切割效率、更好保真度和更少基因组限制的基因编辑工具是当务之急。在这里,我们报道了一种来自粪拟杆菌的 CRISPR/Cas9,其特点是简单的 PAM(5'-NNTA-3')和 21-22 bp 的向导 RNA 长度。我们发现 FrCas9 可以达到与 SpCas9 相当的效率和特异性。有趣的是,FrCas9 的 PAM 呈现出回文序列,这极大地扩展了其靶向范围。由于 PAM 序列,FrCas9 具有双编辑窗口,可直接针对真核启动子中的 TATA 盒,用于 TATA 盒相关疾病。总之,我们的结果拓宽了对 CRISPR/Cas 介导的基因组工程的理解,并确立了 FrCas9 作为一个安全高效的平台,可广泛应用于研究、生物技术和治疗。