Shanghai Center for Plant Stress Biology, Chinese Academy of Sciences, Shanghai, China.
Plant Biotechnol J. 2014 Aug;12(6):797-807. doi: 10.1111/pbi.12200. Epub 2014 May 23.
The CRISPR/Cas9 system has been demonstrated to efficiently induce targeted gene editing in a variety of organisms including plants. Recent work showed that CRISPR/Cas9-induced gene mutations in Arabidopsis were mostly somatic mutations in the early generation, although some mutations could be stably inherited in later generations. However, it remains unclear whether this system will work similarly in crops such as rice. In this study, we tested in two rice subspecies 11 target genes for their amenability to CRISPR/Cas9-induced editing and determined the patterns, specificity and heritability of the gene modifications. Analysis of the genotypes and frequency of edited genes in the first generation of transformed plants (T0) showed that the CRISPR/Cas9 system was highly efficient in rice, with target genes edited in nearly half of the transformed embryogenic cells before their first cell division. Homozygotes of edited target genes were readily found in T0 plants. The gene mutations were passed to the next generation (T1) following classic Mendelian law, without any detectable new mutation or reversion. Even with extensive searches including whole genome resequencing, we could not find any evidence of large-scale off-targeting in rice for any of the many targets tested in this study. By specifically sequencing the putative off-target sites of a large number of T0 plants, low-frequency mutations were found in only one off-target site where the sequence had 1-bp difference from the intended target. Overall, the data in this study point to the CRISPR/Cas9 system being a powerful tool in crop genome engineering.
CRISPR/Cas9 系统已被证明能有效地在多种生物中诱导靶向基因编辑,包括植物。最近的研究表明,在拟南芥中,CRISPR/Cas9 诱导的基因突变在早期世代主要是体细胞突变,尽管一些突变可以在后期世代中稳定遗传。然而,目前尚不清楚该系统在水稻等作物中是否会有类似的效果。在本研究中,我们在两个水稻亚种中测试了 11 个目标基因对 CRISPR/Cas9 诱导编辑的适用性,并确定了基因修饰的模式、特异性和遗传性。对转化植株(T0)第一代的基因型和编辑基因频率的分析表明,CRISPR/Cas9 系统在水稻中非常高效,目标基因在其第一次细胞分裂前的近一半转化胚胎细胞中被编辑。编辑目标基因的纯合子在 T0 植株中很容易找到。基因突变按照经典的孟德尔定律传递到下一代(T1),没有任何新的突变或回复可检测到。即使进行了广泛的搜索,包括全基因组重测序,我们也没有发现本研究中测试的许多目标基因在水稻中存在大规模脱靶的任何证据。通过对大量 T0 植株的潜在脱靶位点进行特异性测序,仅在一个与预期靶标相差 1 个碱基的脱靶位点发现了低频突变。总的来说,本研究的数据表明 CRISPR/Cas9 系统是作物基因组工程的有力工具。