Blanco Francisca, Garretón Virginia, Frey Nicolas, Dominguez Calixto, Pérez-Acle Tomás, Van der Straeten Dominique, Jordana Xavier, Holuigue Loreto
Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, P.O. Box 114-D, Santiago, Chile.
Plant Mol Biol. 2005 Dec;59(6):927-44. doi: 10.1007/s11103-005-2227-x.
Salicylic acid (SA) plays a crucial role in stress resistance in plants by modifying the expression of a battery of genes. In this paper, we report the identification of a group of early SA-regulated genes of Arabidopsis (activated between 0.5-2.5 h), using the cDNA-amplified fragment length polymorphism technique (cDNA-AFLP). Using 128 different primer combinations, we identified several genes based on their differential expression during SA treatment. Among these, we identified 12 genes up-regulated by SA whose patterns of induction were confirmed by Northern analysis. The identified genes can be grouped into two functional groups: Group 1: genes involved in cell protection (i.e. glycosyltransferases, glutathion S-transferases), and Group 2: genes involved in signal transduction (protein kinases and transcription factors). We also evaluated NPR1 requirement for the induction of the 12 up-regulated genes, and found that only those belonging to Group 2 require this co-activator for their expression. In silico analysis of the promoter sequences of the up-regulated genes, allowed us to identify putative cis-elements over-represented in these genes. Interestingly, as-1-like elements, previously characterized as SA-responsive elements, were specifically over-represented in Group 1 genes. The identification of early SA-regulated genes is an important step towards understanding the complex role of this hormone in plant stress resistance.
水杨酸(SA)通过调控一系列基因的表达,在植物抗逆性中发挥关键作用。本文中,我们利用cDNA扩增片段长度多态性技术(cDNA-AFLP),报道了一组拟南芥早期SA调控基因(在0.5-2.5小时内被激活)的鉴定结果。使用128种不同的引物组合,我们基于SA处理期间基因的差异表达鉴定了多个基因。其中,我们鉴定出12个受SA上调的基因,其诱导模式通过Northern分析得以证实。鉴定出的基因可分为两个功能组:第1组:参与细胞保护的基因(即糖基转移酶、谷胱甘肽S-转移酶),以及第2组:参与信号转导的基因(蛋白激酶和转录因子)。我们还评估了NPR1对这12个上调基因诱导的需求,发现只有第2组中的基因表达需要这种共激活因子。对上调基因启动子序列的电子分析,使我们能够鉴定出这些基因中过度富集的假定顺式元件。有趣的是,先前被表征为SA响应元件的as-1样元件,在第1组基因中特异性过度富集。鉴定早期SA调控基因是理解这种激素在植物抗逆性中复杂作用的重要一步。