Ambrosone Alfredo, Batelli Giorgia, Nurcato Roberta, Aurilia Vincenzo, Punzo Paola, Bangarusamy Dhinoth Kumar, Ruberti Ida, Sassi Massimiliano, Leone Antonietta, Costa Antonello, Grillo Stefania
National Research Council of Italy, Institute of Biosciences and Bioresources, Research Division Portici, 80055 Portici (Naples), Italy (A.A., G.B., R.N., P.P., A.C., S.G.);National Research Council of Italy, Institute for Mediterranean Agriculture and Forest Systems, 80056 Ercolano (Naples), Italy (V.A.);Bio-science Core Laboratories, King Abdullah University of Science and Technology, Thuwal 23955-6900, Kingdom of Saudi Arabia (D.K.B.);National Research Council of Italy, Institute of Molecular Biology and Pathology, 00185 Rome, Italy (I.R., M.S.); andDepartment of Pharmacy, University of Salerno, 84084 Fisciano (Salerno), Italy (A.L.).
National Research Council of Italy, Institute of Biosciences and Bioresources, Research Division Portici, 80055 Portici (Naples), Italy (A.A., G.B., R.N., P.P., A.C., S.G.);National Research Council of Italy, Institute for Mediterranean Agriculture and Forest Systems, 80056 Ercolano (Naples), Italy (V.A.);Bio-science Core Laboratories, King Abdullah University of Science and Technology, Thuwal 23955-6900, Kingdom of Saudi Arabia (D.K.B.);National Research Council of Italy, Institute of Molecular Biology and Pathology, 00185 Rome, Italy (I.R., M.S.); andDepartment of Pharmacy, University of Salerno, 84084 Fisciano (Salerno), Italy (A.L.)
Plant Physiol. 2015 May;168(1):292-306. doi: 10.1104/pp.114.255802. Epub 2015 Mar 17.
Salt and drought stress severely reduce plant growth and crop productivity worldwide. The identification of genes underlying stress response and tolerance is the subject of intense research in plant biology. Through microarray analyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycine Glycine (RGG) box-containing RNA-binding protein, whose expression was specifically induced in potato cell cultures gradually exposed to osmotic stress. Here, we show that the Arabidopsis (Arabidopsis thaliana) ortholog, AtRGGA, is a functional RNA-binding protein required for a proper response to osmotic stress. AtRGGA gene expression was up-regulated in seedlings after long-term exposure to abscisic acid (ABA) and polyethylene glycol, while treatments with NaCl resulted in AtRGGA down-regulation. AtRGGA promoter analysis showed activity in several tissues, including stomata, the organs controlling transpiration. Fusion of AtRGGA with yellow fluorescent protein indicated that AtRGGA is localized in the cytoplasm and the cytoplasmic perinuclear region. In addition, the rgga knockout mutant was hypersensitive to ABA in root growth and survival tests and to salt stress during germination and at the vegetative stage. AtRGGA-overexpressing plants showed higher tolerance to ABA and salt stress on plates and in soil, accumulating lower levels of proline when exposed to drought stress. Finally, a global analysis of gene expression revealed extensive alterations in the transcriptome under salt stress, including several genes such as ASCORBATE PEROXIDASE2, GLUTATHIONE S-TRANSFERASE TAU9, and several SMALL AUXIN UPREGULATED RNA-like genes showing opposite expression behavior in transgenic and knockout plants. Taken together, our results reveal an important role of AtRGGA in the mechanisms of plant response and adaptation to stress.
盐胁迫和干旱胁迫严重降低了全球范围内植物的生长和作物产量。鉴定应激反应和耐受性相关的基因是植物生物学领域的研究热点。通过微阵列分析,我们之前在马铃薯(Solanum tuberosum)中鉴定出了StRGGA基因,该基因编码一种含有精氨酸甘氨酸甘氨酸(RGG)框的RNA结合蛋白,其表达在逐渐暴露于渗透胁迫的马铃薯细胞培养物中被特异性诱导。在此,我们表明拟南芥(Arabidopsis thaliana)中的直系同源基因AtRGGA是对渗透胁迫做出适当反应所需的功能性RNA结合蛋白。长期暴露于脱落酸(ABA)和聚乙二醇后,拟南芥幼苗中AtRGGA基因的表达上调,而用NaCl处理则导致AtRGGA基因表达下调。AtRGGA启动子分析表明其在包括气孔(控制蒸腾作用的器官)在内的多个组织中具有活性。AtRGGA与黄色荧光蛋白的融合表明AtRGGA定位于细胞质和细胞质核周区域。此外,在根生长和存活测试中,rgga基因敲除突变体对ABA超敏感,在萌发期和营养生长阶段对盐胁迫也超敏感。过表达AtRGGA的植物在平板和土壤中对ABA和盐胁迫表现出更高的耐受性,在干旱胁迫下积累的脯氨酸水平较低。最后,基因表达的全局分析揭示了盐胁迫下转录组的广泛变化,包括一些基因,如抗坏血酸过氧化物酶2、谷胱甘肽S-转移酶TAU9,以及几个小生长素上调RNA样基因,它们在转基因植物和基因敲除植物中表现出相反的表达行为。综上所述,我们的结果揭示了AtRGGA在植物应激反应和适应机制中的重要作用。