Molla Kutubuddin A, Shih Justin, Wheatley Matthew S, Yang Yinong
Department of Plant Pathology and Environmental Microbiology and the Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA, United States.
ICAR-National Rice Research Institute, Cuttack, India.
Front Genome Ed. 2022 Mar 16;4:825236. doi: 10.3389/fgeed.2022.825236. eCollection 2022.
Canonical CRISPR-Cas9 genome editing technique has profoundly impacted the fields of plant biology, biotechnology, and crop improvement. Since non-homologous end joining (NHEJ) is usually considered to generate random indels, its high efficiency mutation is generally not pertinent to precise editing. Homology-directed repair (HDR) can mediate precise editing with supplied donor DNA, but it suffers from extreme low efficiency in higher plants. Therefore, precision editing in plants will be facilitated by the ability to predict NHEJ repair outcome and to improve HDR efficiency. Here, we report that NHEJ-mediated single nucleotide insertion at different rice genes is predictable based on DNA sequences at the target loci. Three mutation prediction tools (inDelphi, FORECasT, and SPROUT) have been validated in the rice plant system. We also evaluated the chimeric guide RNA (cgRNA) and Cas9-Retron precISe Parallel Editing via homologY (CRISPEY) strategies to facilitate donor template supply for improving HDR efficiency in and rice. However, neither cgRNA nor CRISPEY improved plant HDR editing efficiency in this study. Interestingly, our data indicate that tethering of 200-250 nucleotides long sequence to either 5' or 3' ends of guide RNA did not significantly affect Cas9 cleavage activity.
经典的CRISPR-Cas9基因组编辑技术对植物生物学、生物技术和作物改良领域产生了深远影响。由于非同源末端连接(NHEJ)通常被认为会产生随机插入缺失,其高效突变一般与精确编辑无关。同源定向修复(HDR)可以通过提供的供体DNA介导精确编辑,但在高等植物中其效率极低。因此,预测NHEJ修复结果的能力以及提高HDR效率将有助于植物的精确编辑。在此,我们报告基于目标位点的DNA序列,NHEJ介导的不同水稻基因单核苷酸插入是可预测的。三种突变预测工具(inDelphi、FORECasT和SPROUT)已在水稻植物系统中得到验证。我们还评估了嵌合引导RNA(cgRNA)和通过同源性进行Cas9-逆转录酶精确平行编辑(CRISPEY)策略,以促进供体模板供应,从而提高水稻中的HDR效率。然而,在本研究中,cgRNA和CRISPEY均未提高植物HDR编辑效率。有趣的是,我们的数据表明,在引导RNA的5'或3'末端连接200-250个核苷酸长的序列不会显著影响Cas9的切割活性。