Koh Eugene, Cohen Dekel, Brandis Alexander, Fluhr Robert
Plant and Environmental Sciences, Weizmann Institute of Science, Rehovot, Israel.
Life Sciences Core Facility, Weizmann Institute of Science, Rehovot, Israel.
Plant Cell Environ. 2021 Nov;44(11):3597-3615. doi: 10.1111/pce.14162. Epub 2021 Aug 17.
Singlet oxygen ( O ) production is associated with stress signalling. Here, using Arabidopsis as a model system, we study the effects of the accumulation of 8-hydroxyguanosine (8-oxoG), a major product of O -mediated RNA oxidation. We show that 8-oxoG can accumulate in vivo when O is produced in the cytoplasm. Conditions for such production include the application of RB in the light, dark-to-light transitions in the flu mutant, or subjecting plants to combined dehydration/light exposure. Transcriptomes of these treatments displayed a significant overlap with transcripts stimulated by the cytosolic 80S ribosomal translation inhibitors, cycloheximide and homoharringtonine. We demonstrate that 8-oxoG accumulation correlates with a decrease in RNA translatability, resulting in the rapid decrease of the levels of labile gene repressor elements such as IAA1 and JAZ1 in a proteasome-dependent manner. Indeed, genes regulated by the labile repressors of the jasmonic acid signalling pathway were induced by cycloheximide, RB or dehydration/light treatment independently of the hormone. The results suggest that O , by oxidizing RNA, attenuated cellular translatability and caused specific genes to be released from the repression of their cognate short half-life repressors. The findings here describe a novel means of gene regulation via the direct interaction of O with RNA.
单线态氧(O)的产生与应激信号传导相关。在此,我们以拟南芥为模型系统,研究8-羟基鸟苷(8-oxoG)(O介导的RNA氧化的主要产物)积累的影响。我们发现,当细胞质中产生O时,8-oxoG可在体内积累。产生这种情况的条件包括在光照下施用RB、flu突变体从黑暗到光照的转变,或使植物遭受脱水/光照联合处理。这些处理的转录组与由胞质80S核糖体翻译抑制剂环己酰亚胺和高三尖杉酯碱刺激的转录本有显著重叠。我们证明,8-oxoG的积累与RNA翻译能力的降低相关,导致不稳定基因阻遏元件(如IAA1和JAZ1)的水平以蛋白酶体依赖的方式迅速下降。事实上,茉莉酸信号通路的不稳定阻遏物调控的基因在不依赖激素的情况下,可被环己酰亚胺、RB或脱水/光照处理诱导。结果表明,O通过氧化RNA减弱了细胞的翻译能力,并使特定基因从其同源短半衰期阻遏物的抑制中释放出来。此处的研究结果描述了一种通过O与RNA的直接相互作用进行基因调控的新方式。