Division of Plant Science and Technology, University of Missouri, Columbia, MO, 65211, USA.
Department of Plant Pathology and Institute of Plant Breeding, Genetics and Genomics, University of Georgia, Athens, GA, 30602, USA.
Nat Commun. 2023 Nov 22;14(1):7629. doi: 10.1038/s41467-023-43295-y.
Plant-parasitic nematodes are one of the most economically impactful pests in agriculture resulting in billions of dollars in realized annual losses worldwide. Soybean cyst nematode (SCN) is the number one biotic constraint on soybean production making it a priority for the discovery, validation and functional characterization of native plant resistance genes and genetic modes of action that can be deployed to improve soybean yield across the globe. Here, we present the discovery and functional characterization of a soybean resistance gene, GmSNAP02. We use unique bi-parental populations to fine-map the precise genomic location, and a combination of whole genome resequencing and gene fragment PCR amplifications to identify and confirm causal haplotypes. Lastly, we validate our candidate gene using CRISPR-Cas9 genome editing and observe a gain of resistance in edited plants. This demonstrates that the GmSNAP02 gene confers a unique mode of resistance to SCN through loss-of-function mutations that implicate GmSNAP02 as a nematode virulence target. We highlight the immediate impact of utilizing GmSNAP02 as a genome-editing-amenable target to diversify nematode resistance in commercially available cultivars.
植物寄生线虫是农业中最具经济影响力的害虫之一,导致全球每年损失数十亿美元。大豆胞囊线虫 (SCN) 是大豆生产的头号生物限制因素,因此优先发现、验证和功能表征本土植物抗性基因和遗传作用模式,以提高全球大豆产量。在这里,我们介绍了一个大豆抗性基因 GmSNAP02 的发现和功能表征。我们使用独特的双亲群体来精细映射精确的基因组位置,并结合全基因组重测序和基因片段 PCR 扩增来鉴定和确认因果单倍型。最后,我们使用 CRISPR-Cas9 基因组编辑来验证我们的候选基因,并观察到编辑植物的抗性增加。这表明 GmSNAP02 基因通过功能丧失突变赋予 SCN 独特的抗性模式,暗示 GmSNAP02 是线虫毒力的靶标。我们强调了利用 GmSNAP02 作为基因组编辑可及的靶标来多样化商业上可用品种中线虫抗性的直接影响。