Loupit Grégoire, Valls Fonayet Josep, Tran Joseph, Garcia Virginie, Hummel Irène, Petriacq Pierre, Gallusci Philippe, Berger Margot, Franc Céline, de Revel Gilles, Ollat Nathalie, Cookson Sarah Jane
EGFV, Univ. Bordeaux, Bordeaux Sciences Agro, INRAE, ISVV, F-33882, Villenave d'Ornon, France.
Bordeaux Metabolome Facility, MetaboHUB, PHENOME-EMPHASIS, 33140 Villenave d'Ornon, Talence, France.
Plant J. 2025 Jun;122(5):e70244. doi: 10.1111/tpj.70244.
Grafting plants uses intrinsic wound-healing mechanisms to join together different organisms, yet the processes underpinning graft union formation remain poorly understood. To further our understanding of the molecular reprogramming triggered by grafting and wounding in a perennial plant, we characterised the transcriptome and metabolome of intact and wounded un-grafted scions and rootstocks, and homo- and hetero-grafts at 0 and 14 days after grafting/wounding in grapevine. We show that grafting triggered the coordinated activation of gene expression and the accumulation of lipids and phenolic compounds in comparison with intact tissues. We highlight an asymmetry in gene expression above and below the graft interface, which is in part not only due to carbon status, but also to intrinsic differences in gene expression between un-grafted scions and rootstocks, and their differential responses to wounding. We found that β-1,4-glucanases were differentially expressed in response to both wounding and grafting and demonstrated that exogenous β-1,4-glucanase application increased grafting success rate. Grafting, wounding, homo-graft and hetero-graft-specific transcriptome responses were characterised. The comprehensive experimental design of the dataset containing all necessary control samples allowed the identification of genes and metabolites potentially involved in wounding and grafting responses in an iconic grafted fruit crop. This is important because knowledge of genes regulating graft union formation could be leveraged for the selection of new, highly graft-compatible cultivars in the future.
嫁接植物利用内在的伤口愈合机制将不同的生物体连接在一起,然而,嫁接结合形成的基础过程仍知之甚少。为了进一步了解多年生植物中嫁接和创伤引发的分子重编程,我们对完整的和受伤的未嫁接接穗和砧木,以及葡萄嫁接/创伤后0天和14天的同型和异型嫁接体的转录组和代谢组进行了表征。我们发现,与完整组织相比,嫁接引发了基因表达的协同激活以及脂质和酚类化合物的积累。我们强调了嫁接界面上下基因表达的不对称性,这部分不仅是由于碳状态,还由于未嫁接接穗和砧木之间基因表达的内在差异,以及它们对创伤的不同反应。我们发现β-1,4-葡聚糖酶在对创伤和嫁接的反应中差异表达,并证明外源施用β-1,4-葡聚糖酶可提高嫁接成功率。对嫁接、创伤、同型嫁接和异型嫁接特异性转录组反应进行了表征。包含所有必要对照样本的数据集的全面实验设计,使得能够鉴定出标志性嫁接水果作物中可能参与创伤和嫁接反应的基因和代谢物。这很重要,因为调控嫁接结合形成的基因知识,未来可用于选择新的、高度亲和的嫁接品种。