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Rac-Related GTP-Binding Protein in Elicitor-Induced Reactive Oxygen Generation by Suspension-Cultured Soybean Cells

机译:悬浮培养大豆细胞诱导诱导的活性氧生成中的Rac相关GTP结合蛋白。

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摘要

Plant cells produce reactive oxygen species (ROS) in response to many stimuli. However, the mechanism of ROS biosynthesis remains unclear. We have explored the hypothesis that the superoxide burst in plants mechanistically resembles the oxidative burst in neutrophils. First we have confirmed that ROS production, which occurs in suspension-cultured soybean (Glycine max) cells in response to hypo-osmotic shock, is inhibited by diphenylene iodonium, an inhibitor of the flavin-dependent oxidase of neutrophils. Because a Rac family G protein is an essential regulator of this NADPH oxidase, and because many plant homologs of Rac have been cloned, we next examined whether Rac-like proteins might be involved in the oxidative burst in the soybean cells. We identified a Rac-like 21-kD soybean protein that cross-reacts with antibodies to human Rac and garden pea Rop and also binds [γ-35S] GTP, a diagnostic trait of small G proteins. This Rac-related protein translocated from the cytosol to microsomes during the oxidative burst. Moreover, soybean cells transiently transformed with either a dominant negative (RacN17) or a dominant positive (RacV12) form of Rac1 showed the anticipated altered responses to three different stimuli: hypo-osmotic shock, oligo-GalUA, and harpin. In response to these stimuli, cells transformed with RacN17 produced less ROS and cells transformed with RacV12 generated more ROS than control cells. These results strongly suggest that a Rac-related protein participates in the regulation of ROS production in soybean cells, possibly via activation of an enzyme complex similar to the NADPH oxidase of phagocytes in animal systems.
机译:植物细胞会响应许多刺激而产生活性氧(ROS)。但是,ROS生物合成的机制仍不清楚。我们已经探索了这样的假说,即植物中的超氧化物的爆发机制类似于中性粒细胞的氧化性爆发。首先,我们已经证实,悬浮培养的大豆(Glycine max)细胞因低渗性休克而产生的ROS生成受到中性粒细胞黄素依赖性氧化酶抑制剂联苯亚碘鎓的抑制。由于Rac家族G蛋白是该NADPH氧化酶的必需调节剂,并且由于已经克隆了Rac的许多植物同源物,因此我们接下来检查了Rac样蛋白是否可能参与了大豆细胞的氧化爆发。我们鉴定出一种Rac样21-kD大豆蛋白,它与针对人Rac和菜豌豆Rop的抗体发生交叉反应,并且还结合[γ- 35 S] GTP(一种小G蛋白的诊断特征)。在氧化爆发期间,这种Rac相关蛋白从细胞质转移到微粒体。此外,用显性负(RacN17)或显性正(RacV12)形式的Rac1瞬时转化的大豆细胞显示出对三种不同刺激的预期改变的响应:低渗性休克,低聚GalUA和harpin。响应于这些刺激,与对照细胞相比,用RacN17转化的细胞产生较少的ROS,而用RacV12转化的细胞产生更多的ROS。这些结果强烈表明,Rac相关蛋白可能通过激活类似于动物系统中吞噬细胞的NADPH氧化酶的酶复合物,参与了大豆细胞中ROS的调节。

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