Mazarei Mitra, Puthoff David P, Hart Jennifer K, Rodermel Steven R, Baum Thomas J
Department of Plant Pathology, Iowa State University, Ames 50011, USA.
Mol Plant Microbe Interact. 2002 Jun;15(6):577-86. doi: 10.1094/MPMI.2002.15.6.577.
Ethylene-responsive element-binding proteins (EREBPs) are members of a family of plant transcription factors. Conserved EREBP domains of these proteins bind to the GCC box, an ethylene-responsive promoter element found in many pathogenesis-related (PR) genes. Using degenerate primers to the EREBP domain from diverse plant species, an EREBP homolog was isolated from a soybean cDNA library. Gel mobility-shift assays revealed that the translation product of this cDNA bound specifically to GCC box sequences. We, therefore, named this gene Glycine max ethylene-responsive element-binding protein 1 (GmEREBP1), i.e., a gene coding for the first confirmed GCC box-binding protein of soybean. GmEREBP1 mRNA abundance was analyzed by RNA blot hybridizations in soybean roots and shoots of cultivars Corsoy 79 and Hartwig, which are susceptible and resistant, respectively, to the soybean cyst nematode (Heterodera glycines). These analyses revealed that GmEREBP1 is expressed in a root-preferential manner and that GmEREBP1 mRNA abundance is changed after H. glycines infection. GmEREBP1 mRNA abundance decreased in infected (susceptible) 'Corsoy 79' roots, whereas it increased in abundance in infected (resistant) 'Hartwig' roots. Furthermore, ethephon treatment repressed GmEREBP1 mRNA accumulation in both cultivars, whereas wounding increased expression in both cultivars. These changes in mRNA steady-state levels suggest that GmEREBP1 plays a role in soybean-H. glycines interactions.
乙烯响应元件结合蛋白(EREBPs)是植物转录因子家族的成员。这些蛋白的保守EREBPs结构域与GCC框结合,GCC框是在许多病程相关(PR)基因中发现的乙烯响应启动子元件。利用针对不同植物物种EREBPs结构域的简并引物,从大豆cDNA文库中分离出一个EREBPs同源物。凝胶迁移率变动分析表明,该cDNA的翻译产物与GCC框序列特异性结合。因此,我们将该基因命名为大豆乙烯响应元件结合蛋白1(GmEREBP1),即一个编码大豆首个经证实的GCC框结合蛋白的基因。通过RNA印迹杂交分析了大豆品种Corsoy 79和Hartwig的根和芽中GmEREBP1 mRNA的丰度,这两个品种分别对大豆胞囊线虫(大豆异皮线虫)敏感和抗性。这些分析表明,GmEREBP1以根优先的方式表达,并且在大豆异皮线虫感染后GmEREBP1 mRNA丰度发生变化。在受感染(敏感)的“Corsoy 79”根中,GmEREBP1 mRNA丰度下降,而在受感染(抗性)的“Hartwig”根中,其丰度增加。此外,乙烯利处理抑制了两个品种中GmEREBP1 mRNA的积累,而创伤则增加了两个品种中的表达。mRNA稳态水平的这些变化表明,GmEREBP1在大豆与大豆异皮线虫的相互作用中发挥作用。