清脆的
基因组编辑
Cas9
生物
引导RNA
计算生物学
基因组工程
亚基因组mRNA
遗传学
基因
基因组
水稻
核酸酶
作者
Yanhao Cheng,Gen Li,Aileen Qi,Rushil Mandlik,Changtian Pan,Doris Wang,S Ge,Yiping Qi
标识
DOI:10.1093/plcell/koaf081
摘要
Abstract Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated nuclease (Cas) technologies facilitate routine genome engineering of one or a few genes at a time. However, large-scale CRISPR screens with guide RNA libraries remain challenging in plants. Here, we have developed a comprehensive all-in-one CRISPR toolbox for Cas9-based genome editing, cytosine base editing (CBE), adenine base editing (ABE), Cas12a-based genome editing and ABE, and CRISPR-Act3.0-based gene activation in both monocot and dicot plants. We evaluated all-in-one T-DNA expression vectors in rice (Oryza sativa, monocot) and tomato (Solanum lycopersicum, dicot) protoplasts, demonstrating their broad and reliable applicability. To showcase the applications of these vectors in CRISPR screens, we constructed single guide RNA (sgRNA) pools for testing in rice protoplasts, establishing a high-throughput approach to select high-activity sgRNAs. Additionally, we demonstrated the efficacy of sgRNA library screening for targeted mutagenesis of ACETOLACTATE SYNTHASE in rice, recovering novel candidate alleles for herbicide resistance. Furthermore, we carried out a CRISPR activation screen in Arabidopsis thaliana, rapidly identifying potent sgRNAs for FLOWERING LOCUS T activation that confer an early flowering phenotype. This toolbox contains 61 versatile all-in-one vectors encompassing nearly all commonly used CRISPR technologies. It will facilitate large-scale genetic screens for loss-of-function or gain-of-function studies, presenting numerous promising applications in plants.
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