The LysM receptor-like kinase SlLYK10 controls lipochitooligosaccharide signaling in inner cell layers of tomato roots

Yi Ding, Tongming Wang, Virginie Gasciolli, Guilhem Reyt, Céline Remblière, Fabien Marcel, Tracy François, Abdelhafid Bendahmane, Guanghua He, Jean Jacques Bono, Benoit Lefebvre
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Abstract

Establishment of arbuscular mycorrhiza (AM) relies on a plant signaling pathway that can be activated by fungal chitinic signals such as short chain chitooligosaccharides (CO) and lipo-chitooligosaccharides (LCOs). The tomato LysM receptor-like kinase (LysM RLK) SlLYK10 has high affinity for LCOs and is involved in root colonization by arbuscular mycorrhizal fungi (AMF), however its role in LCO responses has not yet been studied. Here, we show that SlLYK10 proteins produced by the Sllyk10-1 and Sllyk10-2 mutant alleles, which both cause decreases in AMF colonization, and carry mutations in LysM1 and 2 respectively, have similar LCO binding affinities compared to the WT SlLYK10. However, the mutant forms were no longer able to induce cell death in Nicotiana benthamiana when co-expressed with MtLYK3, a Medicago truncatula LCO co-receptor, while they physically interacted with MtLYK3 in co-purification experiments. This suggests that the LysM mutations affect the ability of SlLYK10 to trigger signaling through a potential co-receptor rather than its ability to bind LCOs. Interestingly, tomato lines that contain a calcium (Ca2+) concentration reporter (Genetically Encoded Ca2+ indicators, GECO), showed Ca2+ spiking in response to LCO applications, but this occurred only in inner cell layers of the roots, while short chain COs also induced Ca2+ spiking in the epidermis. Moreover, LCO-induced Ca2+spiking was decreased in Sllyk10-1*GECO plants, suggesting that the decrease in AMF colonization in Sllyk10-1 is due to abnormal LCO signaling.
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LysM受体样激酶SlLYK10控制番茄根内细胞层中的脂寡糖信号转导
丛生菌根(AM)的建立依赖于植物信号通路,该通路可被真菌的几丁质信号(如短链壳寡糖(CO)和脂壳寡糖(LCO))激活。番茄 LysM 受体样激酶(LysM RLK)SlLYK10 与 LCOs 有很高的亲和力,并参与了丛枝菌根真菌(AMF)的根定殖,但它在 LCO 反应中的作用尚未得到研究。在这里,我们发现由 Sllyk10-1 和 Sllyk10-2 突变等位基因产生的 SlLYK10 蛋白与 WT SlLYK10 相比具有相似的 LCO 结合亲和力。然而,当突变体形式与MtLYK3(一种Medicago truncatula LCO共受体)共表达时,它们不再能够诱导烟草中的细胞死亡,而在共纯化实验中,它们与MtLYK3发生了物理相互作用。这表明 LysM 突变影响了 SlLYK10 通过潜在共受体触发信号转导的能力,而不是其结合 LCO 的能力。有趣的是,含有钙(Ca2+)浓度报告因子(基因编码 Ca2+ 指示剂,GECO)的番茄品系在施用 LCO 后出现了 Ca2+ 尖峰反应,但这只发生在根的内细胞层,而短链 CO 也会诱导表皮中的 Ca2+ 尖峰反应。此外,在 Sllyk10-1*GECO 植株中,LCO 诱导的 Ca2+ spiking 减少,这表明 Sllyk10-1 中 AMF 定殖的减少是由于 LCO 信号传导异常所致。
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