Ambrosone Alfredo, Batelli Giorgia, Bostan Hamed, D'Agostino Nunzio, Chiusano Maria Luisa, Perrotta Gaetano, Leone Antonietta, Grillo Stefania, Costa Antonello
National Research Council of Italy, Institute of Biosciences and BioResources, Research Division Portici (CNR-IBBR), Portici (NA), Italy.
Department of Agricultural Sciences, University of Naples "Federico II", Portici (NA), Italy.
Gene. 2017 Jan 15;597:30-39. doi: 10.1016/j.gene.2016.10.024. Epub 2016 Oct 19.
Water-limiting conditions affect dramatically plant growth and development and, ultimately, yield of potato plants (Solanum tuberosum L.). Therefore, understanding the mechanisms underlying the response to water deficit is of paramount interest to obtain drought tolerant potato varieties. Herein, potato 10K cDNA array slides were used to profile transcriptomic changes of two potato cell populations under abrupt (shocked cells) or gradual exposure (adapted cells) to polyethylene glycol (PEG)-mediated water stress. Data analysis identified >1000 differentially expressed genes (DEGs) in our experimental conditions. Noteworthy, our microarray study also suggests that distinct gene networks underlie the cellular response to shock or gradual water stress. On the basis of our experimental findings, it is possible to speculate that DEGs identified in shocked cells participate in early protective and sensing mechanisms to environmental insults, while the genes whose expression was modulated in adapted cells are directly involved in the acquisition of a new cellular homeostasis to cope with water stress conditions. To validate microarray data obtained for potato cells, the expression analysis of 21 selected genes of interest was performed by Real-Time Quantitative Reverse Transcription PCR (qRT-PCR). Intriguingly, the expression levels of these transcripts in 4-week old potato plants exposed to long-term water-deficit. qRT-PCR analysis showed that several genes were regulated similarly in potato cells cultures and tissues exposed to drought, thus confirming the efficacy of our simple experimental system to capture important genes involved in osmotic stress response. Highlighting the differences in gene expression between shock-like and adaptive response, our findings could contribute to the discussion on the biological function of distinct gene networks involved in the response to abrupt and gradual adaptation to water deficit.
水分限制条件会显著影响马铃薯(Solanum tuberosum L.)植株的生长发育,最终影响其产量。因此,了解马铃薯对水分亏缺响应的潜在机制对于培育耐旱马铃薯品种至关重要。在此,利用马铃薯10K cDNA阵列玻片分析了两个马铃薯细胞群体在突然(受冲击细胞)或逐渐暴露(适应细胞)于聚乙二醇(PEG)介导的水分胁迫下的转录组变化。数据分析在我们的实验条件下鉴定出1000多个差异表达基因(DEG)。值得注意的是,我们的微阵列研究还表明,细胞对冲击或逐渐水分胁迫的反应有不同的基因网络作为基础。基于我们的实验结果,可以推测在受冲击细胞中鉴定出的DEG参与了对环境损伤的早期保护和感知机制,而在适应细胞中表达受到调节的基因则直接参与了获得新的细胞稳态以应对水分胁迫条件。为了验证从马铃薯细胞获得的微阵列数据,通过实时定量逆转录PCR(qRT-PCR)对21个选定的感兴趣基因进行了表达分析。有趣的是,这些转录本在暴露于长期水分亏缺的4周龄马铃薯植株中的表达水平。qRT-PCR分析表明,在暴露于干旱的马铃薯细胞培养物和组织中,有几个基因的调控方式相似,从而证实了我们简单实验系统捕捉参与渗透胁迫反应的重要基因的有效性。我们的研究结果突出了类似冲击和适应性反应之间基因表达的差异,可能有助于讨论参与对水分亏缺的突然和逐渐适应反应的不同基因网络的生物学功能。