State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory of Plant Resources, MOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China.
Nat Commun. 2023 Oct 25;14(1):6787. doi: 10.1038/s41467-023-42490-1.
Tandemly arrayed genes (TAGs) with functional redundancy and chromosomal linkage constitute 14 ~ 35% in sequenced plant genomes. The multiplex CRISPR system is the tool of choice for creating targeted TAG deletions. Here, we show that up to ~80% of CRISPR-mediated TAG knockout alleles in Arabidopsis and rice are deletion-inversion (delinver) bi-alleles, which are easily misidentified as homozygous deletion alleles by routine PCR-based genotyping. This can lead to misinterpretation of experimental data and production of progenies with genetic heterogeneity in an unnoticed manner. In ~2,650 transgenic events, delinver mutation frequencies are predominantly correlated with deletion frequencies but unrelated to chromosomal locations or deletion sizes. Delinver mutations also occur frequently at genomic non-TAG loci during multiplexed CRISPR editing. Our work raises the alarm about delinver mutations as common unwanted products of targeted TAG deletions in plants and helps prevent false interpretation of plant TAG functions due to this hidden genotype issue.
串联基因(TAGs)具有功能冗余和染色体连锁,占已测序植物基因组的 14%~35%。多重 CRISPR 系统是创建靶向 TAG 缺失的首选工具。在这里,我们表明,拟南芥和水稻中高达约 80%的 CRISPR 介导的 TAG 敲除等位基因是缺失-倒位(delinver)双等位基因,这些等位基因很容易被常规基于 PCR 的基因分型错误鉴定为纯合缺失等位基因。这可能导致实验数据的误解,并以未被注意的方式产生具有遗传异质性的后代。在约 2650 个转基因事件中,delinver 突变频率主要与缺失频率相关,而与染色体位置或缺失大小无关。在多重 CRISPR 编辑过程中,delinver 突变也经常发生在基因组非 TAG 基因座上。我们的工作提醒人们注意 delinver 突变是植物中靶向 TAG 缺失的常见非预期产物,并有助于防止由于这种隐性基因型问题而对植物 TAG 功能产生错误解释。