Department of Life Sciences and Systems Biology, University of Turin, Turin, 10125, Italy.
The BioActives Lab, Center for Desert Agriculture (CDA), Biological and Environment Science and Engineering (BESE), King Abdullah University of Science and Technology, Thuwal, 23955, Saudi Arabia.
Plant J. 2022 Sep;111(6):1688-1700. doi: 10.1111/tpj.15917. Epub 2022 Aug 17.
The Oryza sativa (rice) carotenoid cleavage dioxygenase OsZAS was described to produce zaxinone, a plant growth-promoting apocarotenoid. A zas mutant line showed reduced arbuscular mycorrhizal (AM) colonization, but the mechanisms underlying this behavior are unknown. Here, we investigated how OsZAS and exogenous zaxinone treatment regulate mycorrhization. Micromolar exogenous supply of zaxinone rescued root growth but not the mycorrhizal defects of the zas mutant, and even reduced mycorrhization in wild-type and zas genotypes. The zas line did not display the increase in the level of strigolactones (SLs) that was observed in wild-type plants at 7 days post-inoculation with AM fungus. Moreover, exogenous treatment with the synthetic SL analog GR24 rescued the zas mutant mycorrhizal phenotype, indicating that the lower AM colonization rate of zas is caused by a deficiency in SLs at the early stages of the interaction, and indicating that during this phase OsZAS activity is required to induce SL production, possibly mediated by the Dwarf14-Like (D14L) signaling pathway. OsZAS is expressed in arbuscule-containing cells, and OsPT11prom::OsZAS transgenic lines, where OsZAS expression is driven by the OsPT11 promoter active in arbusculated cells, exhibit increased mycorrhization compared with the wild type. Overall, our results show that the genetic manipulation of OsZAS activity in planta leads to a different effect on AM symbiosis from that of exogenous zaxinone treatment, and demonstrate that OsZAS influences the extent of AM colonization, acting as a component of a regulatory network that involves SLs.
水稻类胡萝卜素双加氧酶 OsZAS 被描述为产生植物生长促进的脱辅基类胡萝卜素 zaxinone。zas 突变体系显示出减少的丛枝菌根(AM)定殖,但这种行为的机制尚不清楚。在这里,我们研究了 OsZAS 和外源 zaxinone 处理如何调节菌根形成。毫摩尔外源供应的 zaxinone 挽救了根的生长,但不能挽救 zas 突变体的菌根缺陷,甚至在野生型和 zas 基因型中降低了菌根形成。zas 系在接种 AM 真菌 7 天后没有显示出野生型植物中观察到的 Strigolactones (SLs) 水平的增加。此外,用合成的 SL 类似物 GR24 进行外源处理挽救了 zas 突变体的菌根表型,表明 zas 较低的 AM 定殖率是由于在相互作用的早期阶段 SL 缺乏引起的,并且表明在这个阶段 OsZAS 活性是必需的诱导 SL 产生,可能通过 Dwarf14-Like (D14L) 信号通路介导。OsZAS 在含有丛枝的细胞中表达,并且由在丛枝细胞中活跃的 OsPT11 启动子驱动 OsZAS 表达的 OsPT11prom::OsZAS 转基因系与野生型相比表现出增加的菌根形成。总的来说,我们的结果表明,在植物中对 OsZAS 活性的遗传操作对 AM 共生的影响与外源 zaxinone 处理不同,并表明 OsZAS 影响 AM 定殖的程度,作为涉及 SLs 的调节网络的一个组成部分。