Hongyue Zu, Jing Zhang, Weiwei Bai, Peng Kuai, Jingli Cheng, Jing Lu, Yonggen Lou, Ran Li
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引用次数: 0
摘要
多胺(PA)及其共轭形式是植物抵御生物和非生物胁迫的防御机制的重要介质。含黄素的多胺氧化酶(PAOs)通过末端氧化作用调节多胺的水平。迄今为止,人们对 PAOs 在植物与食草动物相互作用中的作用仍知之甚少。我们发现,褐飞虱(BPH)的侵袭破坏了水稻叶鞘内的 PA 平衡,这与 OsPAO6 的上调同时发生,OsPAO6 是一种组织特异性诱导型、定位在叶绿体的酶,可调节亚精胺(Spd)和精胺的末端分解代谢。利用 CRISPR-Cas9 基因组编辑植物进行的功能分析显示,与野生型对照组相比,pao6 突变体在应对 BPH 侵染时积累的 Spd 和苯丙酮结合的 Spd 水平明显更高。此外,BPH 在 pao6 突变体上的取食会导致雌性成虫排出更多的蜜露和对植物的损害,这与 Spd 会增强 BPH 取食的体外实验是一致的。此外,OsPAO6 的转录受茉莉酸盐(JA)信号的调控,并且依赖于 MYC2,后者直接与 OsPAO6 启动子中的 G-box-like motif 结合。我们的研究结果揭示了 OsPAO6 在调节 JA 诱导的水稻多胺分解反应中的重要作用。
Jasmonate-mediated polyamine oxidase 6 drives herbivore-induced polyamine catabolism in rice.
Polyamines (PAs) along with their conjugated forms, are important mediators of plant defense mechanisms against both biotic and abiotic stresses. Flavin-containing polyamine oxidases (PAOs) regulate PA levels through terminal oxidation. To date, the role of PAOs in plant-herbivore interaction remains poorly understood. We discovered that infestation by the brown planthopper (BPH) disrupts PA homeostasis within the leaf sheaths of rice plants, which co-occurs with the upregulation of OsPAO6, a tissue-specific inducible, apoplast-localized enzyme that regulates the terminal catabolism of spermidine (Spd) and spermine. Functional analysis using CRISPR-Cas9 genome-edited plants revealed that pao6 mutants accumulated significantly higher levels of Spd and phenylpropanoid-conjugated Spd in response to BPH infestation compared to wild-type controls. In addition, BPH feeding on pao6 mutants led to increased honeydew excretion and plant damage by female adults, consistent with in vitro experiments in which Spd enhanced BPH feeding. Furthermore, OsPAO6 transcription is regulated by jasmonate (JA) signaling, and it is dependent on MYC2, which directly binds to the G-box-like motif in the OsPAO6 promoter. Our findings reveal an important role of OsPAO6 in regulating polyamine catabolism in JA-induced responses triggered by herbivore attacks in rice.
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.