Ming Meiling, Long Hongjun, Ye Zhicheng, Pan Changtian, Chen Jiali, Tian Rong, Sun Congrui, Xue Yongsong, Zhang Yingxiao, Li Jiaming, Qi Yiping, Wu Jun
College of Horticulture, State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, China.
Department of Plant Science and Landscape Architecture, University of Maryland, College Park, MD 20742, USA.
Hortic Res. 2022 Jun 30;9:uhac148. doi: 10.1093/hr/uhac148. eCollection 2022.
CRISPR/Cas systems have been widely used for genome engineering in many plant species. However, their potentials have remained largely untapped in fruit crops, particularly in pear, due to the high levels of genomic heterozygosity and difficulties in tissue culture and stable transformation. To date, only a few reports on the application of the CRISPR/Cas9 system in pear have been documented, and have shown very low editing efficiency. Here we report a highly efficient CRISPR toolbox for loss-of-function and gain-of-function research in pear. We compared four different CRISPR/Cas9 expression systems for loss-of-function analysis and identified a potent system that showed nearly 100% editing efficiency for multi-site mutagenesis. To expand the targeting scope, we further tested different CRISPR/Cas12a and Cas12b systems in pear for the first time, albeit with low editing efficiency. In addition, we established a CRISPR activation (CRISPRa) system for multiplexed gene activation in pear calli for gain-of-function analysis. Furthermore, we successfully engineered the anthocyanin and lignin biosynthesis pathways using both CRISPR/Cas9 and CRISPRa systems in pear calli. Taking these results together, we have built a highly efficient CRISPR toolbox for genome editing and gene regulation, paving the way for functional genomics studies as well as molecular breeding in pear.
CRISPR/Cas系统已被广泛应用于许多植物物种的基因组工程。然而,由于基因组杂合度高以及组织培养和稳定转化的困难,它们在果树作物,特别是梨中的潜力在很大程度上尚未得到开发。迄今为止,关于CRISPR/Cas9系统在梨中的应用仅有少数报道,且编辑效率非常低。在此,我们报道了一个用于梨功能缺失和功能获得研究的高效CRISPR工具箱。我们比较了四种不同的CRISPR/Cas9表达系统用于功能缺失分析,并确定了一个有效的系统,该系统对多位点诱变显示出近100%的编辑效率。为了扩大靶向范围,我们首次在梨中进一步测试了不同的CRISPR/Cas12a和Cas12b系统,尽管编辑效率较低。此外,我们建立了一个CRISPR激活(CRISPRa)系统,用于梨愈伤组织中的多重基因激活以进行功能获得分析。此外,我们在梨愈伤组织中使用CRISPR/Cas9和CRISPRa系统成功改造了花青素和木质素生物合成途径。综合这些结果,我们构建了一个用于基因组编辑和基因调控的高效CRISPR工具箱,为梨的功能基因组学研究以及分子育种铺平了道路。