Plant Biology Department, Faculty of Science, Shahrekord University, Shahrekord, Iran.
Plant Biology Department, Faculty of Science, Shahrekord University, Shahrekord, Iran; Biotechnology Research Institute, Shahrekord University, Shahrekord, Iran.
J Plant Physiol. 2020 Sep;252:153237. doi: 10.1016/j.jplph.2020.153237. Epub 2020 Jul 16.
In this study, the role of calcium/calmodulin (Ca/CaM) and melatonin (Mel) as two signal molecules in inducing systemic salt tolerance of Dracocephalum kotschyi Boiss. was investigated. Salinity stress (100 mM NaCl) reduced plant growth and induced ionic, osmotic, and oxidative damages in D. kotschyi leaves. Detection of cytosolic free Ca ([Ca]) by the Fura-2 method and the measurement of endogenous Mel by GC-MS demonstrated that salinity induced Ca burst and increased endogenous Mel content in D. kotschyi leaves. Root pretreatment with 5 mM Ca or 100 μM Mel recovered plant growth, reduced leaf electrolytic leakage, HO and MDA contents and improved membrane integrity not only at the application site (roots), but also at the untreated distal parts (leaves) under salt stress. Rhizospheric treatment with Mel and Ca triggered systemic tolerance in D. kotschyi, as judged from improving RWC, increasing proline content, modulating Na, K, and Ca homeostasis, and enhancing the activities of SOD, CAT, APX, and POD in the leaves of salt-stressed plants. Mel augmented [Ca], but the rhizospheric application of Ca antagonists impaired the latter responses. Furthermore, root pretreatment with Ca increased Mel content, but the application of p-chlorophenylalanine (as an inhibitor of Mel biosynthesis) decreased the above attributes in the leaves of Ca-treated plants, leading to an arrest in the Ca-induced systemic salt tolerance. These novel results suggest that interaction of Ca/CaM and Mel is involved in overcoming salt-induced ionic, osmotic, and oxidative damages and Ca and Mel may act as long-distance signals for inducing systemic salt tolerance in D. kotschyi.
在这项研究中,研究了钙/钙调蛋白(Ca/CaM)和褪黑素(Mel)作为两种信号分子在诱导 Dracocephalum kotschyi Boiss. 系统耐盐性中的作用。盐胁迫(100 mM NaCl)降低了植物的生长,并诱导 D. kotschyi 叶片中的离子、渗透和氧化损伤。通过 Fura-2 方法检测细胞质游离 Ca([Ca])和 GC-MS 测量内源性 Mel 表明,盐胁迫诱导 Ca 爆发并增加 D. kotschyi 叶片中的内源性 Mel 含量。用 5 mM Ca 或 100 μM Mel 预处理根,不仅在应用部位(根),而且在盐胁迫下未处理的远端部位(叶)恢复植物生长,降低叶片电解质泄漏、HO 和 MDA 含量,改善膜完整性。Mel 和 Ca 在根际处理引发了 D. kotschyi 的系统耐受性,从提高 RWC、增加脯氨酸含量、调节 Na、K 和 Ca 稳态以及增强盐胁迫下叶片中 SOD、CAT、APX 和 POD 的活性来判断。Mel 增加了[Ca],但根际应用 Ca 拮抗剂会损害后者的反应。此外,用 Ca 预处理根增加了 Mel 含量,但用对氯苯丙氨酸(作为 Mel 生物合成的抑制剂)处理 Ca 处理的植物叶片中的上述特性下降,导致 Ca 诱导的系统耐盐性停止。这些新结果表明,Ca/CaM 和 Mel 的相互作用参与了克服盐诱导的离子、渗透和氧化损伤,Ca 和 Mel 可能作为诱导 D. kotschyi 系统耐盐性的长距离信号。