Yoshida Keisuke, Watanabe Chihiro, Kato Yusuke, Sakamoto Wataru, Noguchi Ko
Department of Biological Sciences, Graduate School of Science, Osaka University, 1-1 Machikaneyama-cho, Toyonaka, Osaka 560-0043, Japan.
Plant Cell Physiol. 2008 Apr;49(4):592-603. doi: 10.1093/pcp/pcn031. Epub 2008 Feb 21.
Mitochondrial alternative oxidase (AOX), the unique respiratory terminal oxidase in plants, catalyzes the energy-wasteful cyanide (CN)-resistant respiration. Although it has been demonstrated that leaf AOX is up-regulated under high-light (HL) conditions, the in vivo mechanism of AOX up-regulation by light is still unknown. In the present study, we examined whether the photo-oxidative stress in the chloroplast modulates mitochondrial respiratory properties, especially the AOX capacity, using Arabidopsis leaf-variegated mutant yellow variegated 2 (var2) and exposing plants to HL. var2 mutants lack FtsH2 metalloprotease required for the repair of damaged PSII. Indeed, var2-1 suffered from photo-oxidative stress even before the HL treatments. While the activities of tricarboxylic acid cycle enzymes and cytochrome c oxidase in var2-1 were almost identical to those in the wild type, the amount of AOX protein and the CN-resistant respiration rate were higher in var2-1. Real-time PCR analysis revealed that HL treatment induced the expression of some energy-dissipating respiratory genes, including AOX1a, NDB2 and UCP5, more strongly in var2-1. Western blotting using var2-1 leaf extracts specific to green or white sectors, containing functional or non-functional photosynthetic apparatus, respectively, revealed that more AOX protein was induced in the green sectors by the HL treatment. These results indicate that photo-oxidative stress by excess light is involved in the regulation of respiratory gene expression and the modulation of respiratory properties, especially the AOX up-regulation.
线粒体交替氧化酶(AOX)是植物中独特的呼吸末端氧化酶,催化消耗能量的抗氰(CN)呼吸。尽管已经证明叶片AOX在高光(HL)条件下会上调,但光上调AOX的体内机制仍不清楚。在本研究中,我们使用拟南芥叶斑驳突变体黄斑驳2(var2)并将植物暴露于高光下,研究叶绿体中的光氧化应激是否调节线粒体呼吸特性,特别是AOX容量。var2突变体缺乏修复受损PSII所需的FtsH2金属蛋白酶。事实上,var2-1甚至在高光处理之前就遭受了光氧化应激。虽然var2-1中三羧酸循环酶和细胞色素c氧化酶的活性与野生型几乎相同,但var2-1中AOX蛋白的量和抗氰呼吸速率更高。实时PCR分析表明,高光处理在var2-1中更强烈地诱导了一些能量耗散呼吸基因的表达,包括AOX1a、NDB2和UCP5。使用分别含有功能性或非功能性光合装置的var2-1叶提取物中绿色或白色部分特异性的蛋白质免疫印迹法显示,高光处理在绿色部分诱导了更多的AOX蛋白。这些结果表明,过量光引起的光氧化应激参与了呼吸基因表达的调节和呼吸特性的调节,特别是AOX的上调。