Willems Patrick, Mhamdi Amna, Stael Simon, Storme Veronique, Kerchev Pavel, Noctor Graham, Gevaert Kris, Van Breusegem Frank
Department of Plant Systems Biology, VIB, 9052 Ghent, Belgium (P.W., A.M., S.S., V.S., P.K., F.V.B.);Department of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium (P.W., A.M., S.S., V.S., P.K., F.V.B.);Medical Biotechnology Center, VIB, 9000 Ghent, Belgium (P.W., S.S., K.G.);Department of Biochemistry, Ghent University, 9000 Ghent, Belgium (P.W., S.S., K.G.);Institut des Sciences des Plantes de Paris-Saclay, Unité Mixte de Recherche 8618, Centre National de la Recherche Scientifique, Université de Paris-Sud, 91405 Orsay cedex, France (A.M., G.N.); andUnité Mixte de Recherche 9213/Unité Mixte de Recherche 1403, Université Paris-Sud, Centre National de la Recherche Scientifique, Institut National de la Recherche Agronomique, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, 91405 Orsay, France (A.M., G.N.).
Department of Plant Systems Biology, VIB, 9052 Ghent, Belgium (P.W., A.M., S.S., V.S., P.K., F.V.B.);Department of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium (P.W., A.M., S.S., V.S., P.K., F.V.B.);Medical Biotechnology Center, VIB, 9000 Ghent, Belgium (P.W., S.S., K.G.);Department of Biochemistry, Ghent University, 9000 Ghent, Belgium (P.W., S.S., K.G.);Institut des Sciences des Plantes de Paris-Saclay, Unité Mixte de Recherche 8618, Centre National de la Recherche Scientifique, Université de Paris-Sud, 91405 Orsay cedex, France (A.M., G.N.); andUnité Mixte de Recherche 9213/Unité Mixte de Recherche 1403, Université Paris-Sud, Centre National de la Recherche Scientifique, Institut National de la Recherche Agronomique, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, 91405 Orsay, France (A.M., G.N.)
Plant Physiol. 2016 Jul;171(3):1720-33. doi: 10.1104/pp.16.00420. Epub 2016 May 31.
In the last decade, microarray studies have delivered extensive inventories of transcriptome-wide changes in messenger RNA levels provoked by various types of oxidative stress in Arabidopsis (Arabidopsis thaliana). Previous cross-study comparisons indicated how different types of reactive oxygen species (ROS) and their subcellular accumulation sites are able to reshape the transcriptome in specific manners. However, these analyses often employed simplistic statistical frameworks that are not compatible with large-scale analyses. Here, we reanalyzed a total of 79 Affymetrix ATH1 microarray studies of redox homeostasis perturbation experiments. To create hierarchy in such a high number of transcriptomic data sets, all transcriptional profiles were clustered on the overlap extent of their differentially expressed transcripts. Subsequently, meta-analysis determined a single magnitude of differential expression across studies and identified common transcriptional footprints per cluster. The resulting transcriptional footprints revealed the regulation of various metabolic pathways and gene families. The RESPIRATORY BURST OXIDASE HOMOLOG F-mediated respiratory burst had a major impact and was a converging point among several studies. Conversely, the timing of the oxidative stress response was a determining factor in shaping different transcriptome footprints. Our study emphasizes the need to interpret transcriptomic data sets in a systematic context, where initial, specific stress triggers can converge to common, aspecific transcriptional changes. We believe that these refined transcriptional footprints provide a valuable resource for assessing the involvement of ROS in biological processes in plants.
在过去十年中,微阵列研究提供了拟南芥(Arabidopsis thaliana)中由各种类型氧化应激引发的信使核糖核酸水平全转录组变化的详尽清单。先前的跨研究比较表明,不同类型的活性氧(ROS)及其亚细胞积累位点能够以特定方式重塑转录组。然而,这些分析通常采用与大规模分析不兼容的简单统计框架。在此,我们重新分析了总共79项关于氧化还原稳态扰动实验的Affymetrix ATH1微阵列研究。为了在如此大量的转录组数据集中建立层次结构,所有转录谱根据其差异表达转录本的重叠程度进行聚类。随后,荟萃分析确定了跨研究的单一差异表达幅度,并识别了每个聚类的共同转录足迹。所得的转录足迹揭示了各种代谢途径和基因家族的调控情况。呼吸爆发氧化酶同源物F介导的呼吸爆发具有重大影响,并且是多项研究中的一个汇聚点。相反,氧化应激反应的时机是塑造不同转录组足迹的一个决定性因素。我们的研究强调了在系统背景下解释转录组数据集的必要性,在这种背景下,最初的特定应激触发因素可以汇聚为共同的、非特异性的转录变化。我们相信,这些精细的转录足迹为评估ROS在植物生物过程中的参与情况提供了宝贵资源。