Zhu Tong, Deng Xing-Guang, Tan Wen-Rong, Zhou Xue, Luo Shi-Shuai, Han Xue-Ying, Zhang Da-Wei, Lin Hong-Hui
Ministry of Education, Key Laboratory for Bio-Resource and Eco-Environment, College of Life Science, State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, Sichuan, China.
Physiol Plant. 2016 Feb;156(2):150-163. doi: 10.1111/ppl.12392. Epub 2015 Nov 6.
Recent studies reported that brassinosteroids (BRs) can induce plant tolerance to different environmental stresses via the nitric oxide (NO) signaling pathway. Previous reports have indicated that alternative oxidase (AOX) plays an important role in plants under various stresses. The mechanisms governing how NO is involved as a signal molecule which connects BR with AOX in regulating stress tolerance are still unknown. Recently, we found that Nicotiana benthamiana seedlings which were pretreated with BR have more tolerance to salt stress, accompanied with an increase of CN-resistant respiration. Our results suggested that pretreatment with 0.1 μM brassinolide (BL, the most active brassinosteroid) alleviated salt-induced oxidative damage and increased the NbAOX1 transcript level. Application of 2-(4-carboxyphenyl)-4,4,5,5-tetramethyl-imidazoline-1-1-oxyl-3-oxide (cPTIO, an NO scavenger) or virus-induced gene silencing of nitrate reductase (NR) and nitric oxide synthase (NOS)-like enzyme compromised the BRs-induced alternative respiratory pathway. Furthermore, pretreatment with specific chemical inhibitors of NR and NOS or gene silencing experiments decreased plant resistance to salt stress which also compromised BRs-induced salt stress tolerance. In conclusion, NO is involved in BRs-induced AOX capability which plays essential roles in salt tolerance in N. benthamiana seedlings.
最近的研究报道,油菜素甾醇(BRs)可通过一氧化氮(NO)信号通路诱导植物对不同环境胁迫的耐受性。此前的报道表明,交替氧化酶(AOX)在植物应对各种胁迫时发挥重要作用。然而,关于NO作为连接BR与AOX以调节胁迫耐受性的信号分子的具体作用机制仍不清楚。最近,我们发现用BR预处理的本氏烟草幼苗对盐胁迫具有更强的耐受性,同时伴随着抗氰呼吸的增加。我们的结果表明,用0.1μM油菜素内酯(BL,活性最强的油菜素甾醇)预处理可减轻盐胁迫诱导的氧化损伤,并提高NbAOX1转录水平。应用2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基-3-氧化物(cPTIO,一种NO清除剂)或通过病毒诱导的硝酸还原酶(NR)和一氧化氮合酶(NOS)样酶基因沉默会损害BRs诱导的交替呼吸途径。此外,用NR和NOS的特异性化学抑制剂预处理或进行基因沉默实验会降低植物对盐胁迫的抗性,这也会损害BRs诱导的盐胁迫耐受性。总之,NO参与了BRs诱导的AOX活性,这在本氏烟草幼苗的耐盐性中起着至关重要的作用。