A comprehensive all-in-one CRISPR toolbox for large-scale screens in plants

Yanhao Cheng, Gen Li, Aileen Qi, Rushil Mandlik, Changtian Pan, Doris Wang, Sophia Ge, Yiping Qi
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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.
一个全面的一体化CRISPR工具箱,用于植物的大规模筛选
聚集规则间隔短回文重复序列(CRISPR)-CRISPR相关核酸酶(Cas)技术促进了一次一个或几个基因的常规基因组工程。然而,在植物中利用引导RNA文库进行大规模CRISPR筛选仍然具有挑战性。在这里,我们开发了一个全面的一体化CRISPR工具箱,用于基于cas9的基因组编辑、胞嘧啶碱基编辑(CBE)、腺嘌呤碱基编辑(ABE)、基于cas12的基因组编辑和ABE,以及基于CRISPR- act3.0的单子叶和双子叶植物基因激活。我们在水稻(Oryza sativa, monocot)和番茄(Solanum lycopersicum, dicot)原生质体中评估了一体化T-DNA表达载体,证明了它们广泛可靠的适用性。为了展示这些载体在CRISPR筛选中的应用,我们构建了单向导RNA (sgRNA)池,用于水稻原生质体的测试,建立了一种高通量筛选高活性sgRNA的方法。此外,我们还证明了sgRNA文库筛选对水稻乙酰乳酸合成酶靶向诱变的有效性,恢复了新的抗除草剂候选等位基因。此外,我们在拟南芥中进行了CRISPR激活筛选,快速鉴定了开花位点T激活的有效sgrna,这些sgrna赋予了早期开花表型。这个工具箱包含61个多功能的一体化载体,涵盖了几乎所有常用的CRISPR技术。它将促进功能丧失或功能获得研究的大规模遗传筛选,在植物中呈现出许多有前途的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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