CRISPR/Cas9-driven double modification of grapevine MLO6-7 imparts powdery mildew resistance, while editing of NPR3 augments powdery and downy mildew tolerance.

IF 6.2 1区 生物学 Q1 PLANT SCIENCES The Plant Journal Pub Date : 2024-12-08 DOI:10.1111/tpj.17204
Loredana Moffa, Giuseppe Mannino, Ivan Bevilacqua, Giorgio Gambino, Irene Perrone, Chiara Pagliarani, Cinzia Margherita Bertea, Alberto Spada, Anna Narduzzo, Elisa Zizzamia, Riccardo Velasco, Walter Chitarra, Luca Nerva
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Abstract

The implementation of genome editing strategies in grapevine is the easiest way to improve sustainability and resilience while preserving the original genotype. Among others, the Mildew Locus-O (MLO) genes have already been reported as good candidates to develop powdery mildew-immune plants. A never-explored grapevine target is NPR3, a negative regulator of the systemic acquired resistance. We report the exploitation of a cisgenic approach with the Cre-lox recombinase technology to generate grapevine-edited plants with the potential to be transgene-free while preserving their original genetic background. The characterization of three edited lines for each target demonstrated immunity development against Erysiphe necator in MLO6-7-edited plants. Concomitantly, a significant improvement of resilience, associated with increased leaf thickness and specific biochemical responses, was observed in defective NPR3 lines against E. necator and Plasmopara viticola. Transcriptomic analysis revealed that both MLO6-7 and NPR3 defective lines modulated their gene expression profiles, pointing to distinct though partially overlapping responses. Furthermore, targeted metabolite analysis highlighted an overaccumulation of stilbenes coupled with an improved oxidative scavenging potential in both editing targets, likely protecting the MLO6-7 mutants from detrimental pleiotropic effects. Finally, the Cre-loxP approach allowed the recovery of one MLO6-7 edited plant with the complete removal of transgene. Taken together, our achievements provide a comprehensive understanding of the molecular and biochemical adjustments occurring in double MLO-defective grape plants. In parallel, the potential of NPR3 mutants for multiple purposes has been demonstrated, raising new questions on its wide role in orchestrating biotic stress responses.

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CRISPR/ cas9驱动的葡萄MLO6-7双修饰增强了葡萄的白粉病抗性,而NPR3的编辑增强了葡萄的白粉病和霜霉病抗性。
在葡萄藤中实施基因组编辑策略是在保留原始基因型的同时提高可持续性和恢复力的最简单方法。其中,霉病基因座o (MLO)基因已经被报道为培育白粉病免疫植物的良好候选者。一个从未被探索过的小道消息靶点是NPR3,它是系统性获得性耐药的负调节因子。我们报道了利用Cre-lox重组酶技术的顺基因方法来产生葡萄藤编辑植物,这些植物在保留其原始遗传背景的同时具有无转基因的潜力。针对每个靶点的三个编辑系的特性表明,在mlo6 -7编辑的植物中,对赤毒杆菌产生了免疫。与此同时,在NPR3缺陷株系中,抗逆性显著提高,与叶片厚度增加和特定生化反应有关。转录组学分析显示,MLO6-7和NPR3缺陷系都调节了它们的基因表达谱,表明它们的反应不同,但部分重叠。此外,靶向代谢物分析强调了两种编辑靶标中二苯乙烯的过度积累以及氧化清除潜力的改善,可能保护MLO6-7突变体免受有害的多效性影响。最后,Cre-loxP方法允许在完全去除转基因的情况下恢复一株MLO6-7编辑的植物。综上所述,我们的成果提供了对双mlo缺陷葡萄植株中发生的分子和生化调节的全面理解。同时,NPR3突变体具有多种用途的潜力,这就对其在协调生物应激反应中的广泛作用提出了新的问题。
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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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