Papikian Ashot, Rattner Rachel J, Kao Jenni, Hauser Neil, Allsing Nicholas, Mamerto Allen, Hartwick Nolan T, Colt Kelly, Michael Todd P
Plant Molecular and Cellular Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Department of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, La Jolla, CA 92093.
Proc Natl Acad Sci U S A. 2025 Aug 19;122(33):e2419744122. doi: 10.1073/pnas.2419744122. Epub 2025 Aug 11.
Plant genomes have undergone multiple rounds of whole-genome duplication (WGD) throughout their evolutionary history. As a result, many species, including , retain duplicated genomic segments, or syntenic regions, which harbor large numbers of paralogous genes preserved from these ancient WGD events. We deleted four large, duplicated blocks, ranging from ~115 kb to ~684 kb using Cas9 to explore the effects of knocking out these blocks in . Large deletions like these remain rare, especially in small and gene-dense plant genomes. Deletions were subsequently verified using whole-genome sequencing, which revealed minimal off-target effects. The number of deleted genes ranged from 16 to 60, and transposable elements ranged from 4 to 112 among the four deleted blocks. Two deletion lines showed distinct phenotypes resulting from the loss of many genes, while two others displayed no obvious defects, including for flowering time or hypocotyl elongation. Moreover, RNA-sequencing revealed that expression compensation, where deletions of paralogous genes lead to the upregulation of intact paralogues, was not a general response to the deleted regions under the conditions tested. Thus, it is possible to obtain viable plants when deleting large fragments that may be redundant or that contain nonessential genes. These results demonstrate that large chromosomal deletions can be used as a tool for genome engineering approaches, such as genome minimization in plants and allele replacement using homology-directed repair and other precision editing methods. Targeted deletions of large chromosome fragments will be a valuable tool for research and biotechnology applications.
植物基因组在其整个进化历史中经历了多轮全基因组复制(WGD)。因此,包括[具体物种未给出]在内的许多物种保留了重复的基因组片段或同线区域,这些区域含有大量从这些古老的WGD事件中保留下来的旁系同源基因。我们使用Cas9删除了四个大的重复片段,大小从约115 kb到约684 kb,以探索在[具体物种未给出]中敲除这些片段的影响。像这样的大缺失仍然很少见,尤其是在小的、基因密集的植物基因组中。随后使用全基因组测序验证了缺失情况,结果显示脱靶效应极小。在四个被删除的片段中,被删除的基因数量从16个到60个不等,转座元件数量从4个到112个不等。两个缺失系由于许多基因的缺失表现出明显的表型,而另外两个则没有明显缺陷,包括开花时间或下胚轴伸长方面。此外,RNA测序表明,在测试条件下,旁系同源基因的缺失导致完整旁系同源基因上调的表达补偿,并非对被删除区域的普遍反应。因此,删除可能冗余或包含非必需基因的大片段时有可能获得有活力的植株。这些结果表明,大的染色体缺失可作为基因组工程方法的一种工具,例如植物基因组最小化以及使用同源定向修复和其他精确编辑方法进行等位基因替换。靶向删除大的染色体片段将是研究和生物技术应用的一个有价值的工具。