Department of Botany, Faculty of Biology, University of Athens, Athens, Greece.
Cytoskeleton (Hoboken). 2012 Jan;69(1):1-21. doi: 10.1002/cm.20538. Epub 2011 Oct 18.
In this study, the effects of disturbance of the reactive oxygen species (ROS) homeostasis on the organization of tubulin cytoskeleton in interphase and mitotic root-tip cells of Triticum turgidum and Arabidopsis thaliana were investigated. Reduced ROS levels were obtained by treatment with diphenylene iodonium (DPI) and N-acetyl-cysteine, whereas menadione was applied to achieve ROS overproduction. Both increased and low ROS levels induced: (a) Macrotubule formation in cells with low ROS levels and tubulin paracrystals under oxidative stress. The protein MAP65-1 was detected in treated cells, exhibiting a conformation comparable to that of the atypical tubulin polymers. (b) Disappearance of microtubules (MTs). (c) Inhibition of preprophase band formation. (d) Delay of the nuclear envelope breakdown at prometaphase. (e) Prevention of perinuclear tubulin polymer assembly in prophase cells. (f) Loss of bipolarity of prophase, metaphase and anaphase spindles. Interestingly, examination of the A. thaliana rhd2/At respiratory burst oxidase homolog C (rbohc) NADPH oxidase mutant, lacking RHD2/AtRBOHC, gave comparable results. Similarly to DPI, the decreased ROS levels in rhd2 root-tip cells, interfered with MT organization and induced macrotubule assembly. These data indicate, for first time in plants, that ROS are definitely implicated in: (a) mechanisms controlling the assembly/disassembly of interphase, preprophase and mitotic MT systems and (b) mitotic spindle function. The probable mechanisms, by which ROS affect these processes, are discussed.
在这项研究中,研究了活性氧(ROS)稳态紊乱对小麦和拟南芥间期和有丝分裂根尖细胞中微管骨架组织的影响。通过使用二苯基碘(DPI)和 N-乙酰半胱氨酸处理来降低 ROS 水平,而应用甲萘醌来实现 ROS 过度产生。ROS 水平升高和降低都会诱导:(a)ROS 水平低的细胞中形成大微管和氧化应激下的微管副晶体。在处理过的细胞中检测到 MAP65-1 蛋白,其构象与非典型微管聚合物相似。(b)微管(MTs)消失。(c)前期带形成受阻。(d)前中期核膜破裂延迟。(e)阻止前期细胞中核周微管聚合物的组装。(f)前期、中期和后期纺锤体的两极性丧失。有趣的是,对拟南芥 rhd2/At 呼吸爆发氧化酶同源物 C(rbohc)NADPH 氧化酶突变体(缺乏 RHD2/AtRBOHC)的检查也得到了类似的结果。与 DPI 类似,rhd2 根尖细胞中 ROS 水平降低,干扰了 MT 组织并诱导大微管组装。这些数据首次表明,ROS 确实参与了:(a)控制间期、前期和有丝分裂 MT 系统组装/解组装的机制,以及(b)有丝分裂纺锤体功能。讨论了 ROS 影响这些过程的可能机制。