ICAR-National Rice Research Institute, Cuttack, 753006, India.
Department of Botany, Ravenshaw University, Cuttack, 753003, India.
Plant Cell Rep. 2024 Nov 23;43(12):291. doi: 10.1007/s00299-024-03371-z.
A long tracrRNA (tracr-L), which naturally act as single guide RNA, and its truncated version, Δtracr-L, from S. pyogenes, efficiently induce Cas9-mediated double-strand breaks (DSBs) in plant genomic loci, as demonstrated by in vitro cleavage assay and protoplast transfection. CRISPR-Cas system provides a form of immune memory in prokaryotes and archaea, protecting them against viruses and foreign genetic elements. In Streptococcus pyogenes, this system includes the pre-crRNA along with another non-coding RNA, tracrRNA, which aids in CRISPR-based immunity. In S. pyogenes, two distinct tracrRNAs are produced: a long form (tracr-L) and a short form (tracr-S). The tracr-S regulates crRNA biogenesis and Cas9 cleavage, while tracr-L suppresses CRISPR-Cas expression by targeting the Cas9 promoter to prevent autoimmunity. Deleting 79 nucleotides from tracr-L results in Δtracr-L, which retains similar functionality in gene repression. This study investigates, for the first time, the effectiveness of tracr-L, and Δtracr-L in genome editing within plant systems. In vitro cleavage assays using purified Cas9 and synthesized sgRNAs targeting the Cas9 gene, OsPDS, and the OsSWEET11 promoter revealed that across all target sites, tracr-S demonstrated the highest cleavage efficiency compared to tracr-L and Δtracr-L. For in vivo genome editing, we transfected rice protoplasts with tracr-L, Δtracr-L, and tracr-S, targeting three rice genes: OsPDS, OsSPL14, and the promoter of OsSWEET14. Amplicon deep sequencing revealed various types of indels at the target regions across all three tracrRNA versions, indicating comparable levels of efficiency. This study establishes the utility of both the long-form tracrRNA (tracr-L) and its truncated variant (Δtracr-L) in eukaryote genome editing. These two new forms of tracrRNA provide proof of concept and expand the CRISPR-Cas toolkit for plant genome editing applications, and for eukaryotes more broadly.
一段长的 tracrRNA(tracr-L),它自然充当单指导 RNA,及其截短版本 Δtracr-L,来自酿脓链球菌,有效地诱导 Cas9 介导的双链断裂(DSBs)在植物基因组基因座中,通过体外切割试验和原生质体转染证明。CRISPR-Cas 系统在原核生物和古菌中提供了一种免疫记忆形式,保护它们免受病毒和外源遗传元件的侵害。在酿脓链球菌中,该系统包括预 crRNA 以及另一种非编码 RNA tracrRNA,它有助于基于 CRISPR 的免疫。在酿脓链球菌中,产生了两种不同的 tracrRNA:一种长形式(tracr-L)和一种短形式(tracr-S)。tracr-S 调节 crRNA 生物发生和 Cas9 切割,而 tracr-L 通过靶向 Cas9 启动子来抑制 CRISPR-Cas 表达,以防止自身免疫。从 tracr-L 中删除 79 个核苷酸会导致Δtracr-L,它在基因抑制中保留了类似的功能。本研究首次研究了 tracr-L 和Δtracr-L 在植物系统内基因组编辑中的有效性。使用纯化的 Cas9 和针对 Cas9 基因 OsPDS 和 OsSWEET11 启动子的合成 sgRNA 进行的体外切割试验表明,在所有靶位点中,与 tracr-L 和Δtracr-L 相比,tracr-S 显示出最高的切割效率。对于体内基因组编辑,我们用 tracr-L、Δtracr-L 和 tracr-S 转染水稻原生质体,靶向三个水稻基因:OsPDS、OsSPL14 和 OsSWEET14 启动子。扩增子深度测序显示,在所有三种 tracrRNA 版本中,靶区域都存在各种类型的插入缺失,表明效率相当。本研究确立了长形式 tracrRNA(tracr-L)及其截短变体(Δtracr-L)在真核生物基因组编辑中的有效性。这两种新形式的 tracrRNA 为植物基因组编辑应用和更广泛的真核生物提供了概念验证,并扩展了 CRISPR-Cas 工具包。