Adaptation of bacterial natural single guide RNA (tracr-L) for efficient plant genome editing.

IF 5.3 2区 生物学 Q1 PLANT SCIENCES Plant Cell Reports Pub Date : 2024-11-23 DOI:10.1007/s00299-024-03371-z
Subhasis Karmakar, Debasmita Panda, Deeptirekha Behera, Romio Saha, Mirza J Baig, Kutubuddin Ali Molla
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Abstract

Key message: 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.

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将细菌天然单导 RNA(tracr-L)用于高效植物基因组编辑。
关键信息体外裂解试验和原生质体转染证明,来自化脓性链球菌的长tracrRNA(tracr-L)可作为单导RNA,其截短版本Δtracr-L可有效诱导Cas9介导的植物基因组位点双链断裂(DSB)。CRISPR-Cas 系统为原核生物和古生物提供了一种免疫记忆,保护它们免受病毒和外来遗传因子的侵害。在化脓性链球菌中,该系统包括 pre-crRNA 和另一种非编码 RNA--tracrRNA,后者有助于实现基于 CRISPR 的免疫。在化脓性球菌中,会产生两种不同的 tracrRNA:长型(tracr-L)和短型(tracr-S)。tracr-S调节crRNA的生物发生和Cas9的裂解,而tracr-L则通过靶向Cas9启动子抑制CRISPR-Cas的表达,以防止自身免疫。从tracr-L中删除79个核苷酸后,就得到了Δtracr-L,它在基因抑制方面保留了类似的功能。本研究首次研究了 tracr-L 和 Δtracr-L 在植物系统内进行基因组编辑的有效性。使用纯化的Cas9和合成的靶向Cas9基因、OsPDS和OsSWEET11启动子的sgRNA进行体外裂解试验发现,在所有靶位点上,tracr-S的裂解效率都高于tracr-L和Δtracr-L。为了进行体内基因组编辑,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的启动子。扩增子深度测序显示,所有三种 tracrRNA 的靶区都存在各种类型的嵌合体,表明其效率相当。这项研究确定了长形 tracrRNA(tracr-L)及其截短变体(Δtracr-L)在真核生物基因组编辑中的用途。这两种新形式的 tracrRNA 提供了概念证明,扩大了 CRISPR-Cas 在植物基因组编辑应用以及更广泛的真核生物中的工具包。
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来源期刊
Plant Cell Reports
Plant Cell Reports 生物-植物科学
CiteScore
10.80
自引率
1.60%
发文量
135
审稿时长
3.2 months
期刊介绍: Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as: - genomics and genetics - metabolism - cell biology - abiotic and biotic stress - phytopathology - gene transfer and expression - molecular pharming - systems biology - nanobiotechnology - genome editing - phenomics and synthetic biology The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.
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