Dep. of Plant Science and Landscape Architecture, Univ. of Maryland, College Park, MD, 20742, USA.
Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding/Jiangsu Key Laboratory of Crop Genetics and Physiology, Agricultural College of Yangzhou Univ., Yangzhou, 225009, China.
Plant Genome. 2023 Jun;16(2):e20266. doi: 10.1002/tpg2.20266. Epub 2022 Sep 30.
Clustered regularly interspaced short palindromic repeats (CRISPR) nucleases like Cas9 and Cas12a are revolutionizing plant basic research and crop breeding. A major advantage of CRISPR over earlier nucleases systems is its capability of multiplexed genome editing. However, it remains unknown about the potential off-target effects when multiple concurrent DNA double-strand breaks (DSBs) are induced in a crop genome. Here, we investigated this important question in rice (Oryza sativa) using a highly multiplexed CRISPR-Cas12a system. With whole-genome sequencing, we first revealed high genome editing specificity of Mb2Cas12a and protospacer adjacent motif promiscuity of LbCas12a. We discovered large chromosomal rearrangement events in edited rice plants that endured many (e.g., >50) simultaneous DSBs, but not in plants that endured lower order DSBs (e.g., <10). Our results shed important light on the analysis and regulation of engineered crops derived from CRISPR-Cas mediated multiplexed genome editing.
成簇规律间隔短回文重复 (CRISPR) 核酸酶,如 Cas9 和 Cas12a,正在彻底改变植物基础研究和作物育种。与早期的核酸酶系统相比,CRISPR 的一个主要优势是其能够进行多重基因组编辑。然而,当在作物基因组中同时诱导多个 DNA 双链断裂 (DSB) 时,其潜在的脱靶效应仍不清楚。在这里,我们使用高度多重的 CRISPR-Cas12a 系统在水稻 (Oryza sativa) 中研究了这个重要问题。通过全基因组测序,我们首先揭示了 Mb2Cas12a 的高度基因组编辑特异性和 LbCas12a 的原间隔基序 (PAM) 混杂性。我们在编辑的水稻植物中发现了大的染色体重排事件,这些植物承受了许多(例如,>50)同时的 DSB,但在承受较低数量 DSB 的植物中没有发现(例如,<10)。我们的结果为分析和调控源自 CRISPR-Cas 介导的多重基因组编辑的工程作物提供了重要的启示。