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抑制玉米类血朊素 ZmPgb1.1 促进植物对草分枝杆菌的耐受性。

Suppression of the maize phytoglobin ZmPgb1.1 promotes plant tolerance against Clavibacter nebraskensis.

机构信息

Department of Plant Science, University of Manitoba, Winnipeg, MB, R3T 2N2, Canada.

Department of Botany, Faculty of Science, Tanta University, Tanta, 31527, Egypt.

出版信息

Planta. 2019 Dec;250(6):1803-1818. doi: 10.1007/s00425-019-03263-7. Epub 2019 Aug 27.

Abstract

Suppression of the maize phytoglobin ZmPgb1.1 enhances tolerance against Clavibacter nebraskensis by promoting hypersensitive response mechanisms mediated by ethylene and reactive oxygen species. Suppression of the maize phytoglobin, ZmPgb1.1, reduced lesion size and disease severity in leaves following inoculation with Clavibacter nebraskensis, the causal agent of Goss's bacterial wilt disease of corn. These effects were associated with an increase of the transcriptional levels of ethylene biosynthetic and responsive genes, which resulted in the accumulation of reactive oxygen species (ROS) and TUNEL-positive nuclei in the proximity of the inoculation site. An in vitro system, in which maize cells were treated with induced xylem sap, was employed to define the cause-effect relationship of these events. Phytoglobins (Pgbs) are hemoglobins able to scavenge nitric oxide (NO). Suppression of ZmPgb1.1 elevated the level of NO in cells exposed to the induced xylem sap causing a rise in the transcript levels of ethylene biosynthesis and response genes, as well as ethylene. Accumulation of ethylene in the same cells was sufficient to elevate the amount of reactive oxygen species (ROS), through the activation of the respiratory burst oxidase homologs (Rboh) genes, and trigger programmed cell death (PCD). The sequence of these events was demonstrated by manipulating the content of NO and ethylene in culture through pharmacological treatments. Collectively, our results illustrated that suppression of ZmPgb1.1 evokes tolerance against C. nebraskensis culminating in the execution of PCD, a key step of the hypersensitive response.

摘要

抑制玉米植物血球蛋白 ZmPgb1.1 通过促进乙烯和活性氧介导的过敏反应机制增强对 Clavibacter nebraskensis 的耐受性。抑制玉米植物血球蛋白 ZmPgb1.1 可减少接种 Clavibacter nebraskensis(玉米细菌性萎蔫病的病原体)后叶片的损伤大小和严重程度。这些效应与乙烯生物合成和响应基因转录水平的增加有关,导致活性氧 (ROS) 和 TUNEL 阳性核在接种部位附近积累。采用体外系统,用诱导的木质部汁液处理玉米细胞,以定义这些事件的因果关系。植物血球蛋白 (Pgbs) 是能够清除一氧化氮 (NO) 的血红蛋白。抑制 ZmPgb1.1 可提高暴露于诱导木质部汁液的细胞中 NO 的水平,从而导致乙烯生物合成和响应基因以及乙烯的转录水平升高。同一细胞中乙烯的积累足以通过激活呼吸爆发氧化酶同源物 (Rboh) 基因来提高活性氧 (ROS) 的量,并引发程序性细胞死亡 (PCD)。通过药理学处理来操纵培养物中 NO 和乙烯的含量,证明了这些事件的顺序。总之,我们的结果表明,抑制 ZmPgb1.1 可引发对 C. nebraskensis 的耐受性,最终导致 PCD 的执行,这是过敏反应的关键步骤。

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