College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, PR China.
J Exp Bot. 2010 Oct;61(15):4399-411. doi: 10.1093/jxb/erq243. Epub 2010 Aug 6.
Brassinosteroids (BRs) have been shown to induce hydrogen peroxide (H(2)O(2)) accumulation, and BR-induced H(2)O(2) up-regulates antioxidant defence systems in plants. However, the mechanisms by which BR-induced H(2)O(2) regulates antioxidant defence systems in plants remain to be determined. In the present study, the role of ZmMPK5, a mitogen-activated protein kinase, in BR-induced anitioxidant defence and the relationship between the activation of ZmMPK5 and H(2)O(2) production in BR signalling were investigated in leaves of maize (Zea mays) plants. BR treatment activated ZmMPK5, induced apoplastic and chloroplastic H(2)O(2) accumulation, and enhanced the total activities of antioxidant enzymes. Such enhancements were blocked by pre-treatment with mitogen-activated protein kinase kinase (MAPKK) inhibitors and H(2)O(2) inhibitors or scavengers. Pre-treatment with MAPKK inhibitors substantially arrested the BR-induced apoplastic H(2)O(2) production after 6 h of BR treatment, but did not affect the levels of apoplastic H(2)O(2) within 1 h of BR treatment. BR-induced gene expression of NADPH oxidase was also blocked by pre-treatment with MAPKK inhibitors and an apoplastic H(2)O(2) inhibitor or scavenger after 120 min of BR treatment, but was not affected within 30 min of BR treatment. These results suggest that the BR-induced initial apoplastic H(2)O(2) production activates ZmMPK5, which is involved in self-propagation of apoplastic H(2)O(2) via regulation of NADPH oxidase gene expression in BR-induced antioxidant defence systems.
油菜素内酯(BRs)已被证明能诱导过氧化氢(H2O2)的积累,并且 BR 诱导的 H2O2 上调植物中的抗氧化防御系统。然而,BR 诱导的 H2O2 调节植物抗氧化防御系统的机制仍有待确定。在本研究中,研究了丝裂原活化蛋白激酶 ZmMPK5 在 BR 诱导的抗氧化防御中的作用,以及 ZmMPK5 的激活与 BR 信号转导中 H2O2 产生之间的关系,该研究以玉米(Zea mays)叶片为材料。BR 处理激活了 ZmMPK5,诱导了质外体和叶绿体 H2O2 的积累,并增强了抗氧化酶的总活性。MAPKK 抑制剂和 H2O2 抑制剂或清除剂预处理可阻断这些增强作用。MAPKK 抑制剂预处理在 BR 处理 6 小时后,大大阻止了 BR 诱导的质外体 H2O2 的产生,但不影响 BR 处理 1 小时内质外体 H2O2 的水平。MAPKK 抑制剂和质外体 H2O2 抑制剂或清除剂预处理也可阻断 BR 诱导的 NADPH 氧化酶基因表达在 BR 处理 120 分钟后,但在 BR 处理 30 分钟内不受影响。这些结果表明,BR 诱导的初始质外体 H2O2 产生激活了 ZmMPK5,它通过调节 BR 诱导的抗氧化防御系统中 NADPH 氧化酶基因的表达,参与了质外体 H2O2 的自我传播。