Kim Kang-Chang, Fan Baofang, Chen Zhixiang
Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907-2054, USA.
Plant Physiol. 2006 Nov;142(3):1180-92. doi: 10.1104/pp.106.082487. Epub 2006 Sep 8.
The Arabidopsis (Arabidopsis thaliana) WRKY7 gene is induced by pathogen infection and salicylic acid (SA) treatment and may therefore play a role in plant defense responses. Here, we show that WRKY7 is localized in the nucleus, recognizes DNA molecules with the W-box (TTGAC) elements, and functions as a transcriptional repressor in plant cells. To study its biological functions directly, we have characterized both loss-of-function T-DNA insertion and RNAi mutants and gain-of-function transgenic overexpression plants for WRKY7 in Arabidopsis. The T-DNA insertion and RNAi mutant plants displayed enhanced resistance to a virulent strain of the bacterial pathogen Pseudomonas syringae as measured by significant decrease in both bacterial growth and symptom development as compared to those in wild-type plants. The enhanced resistance in the loss-of-function mutants was associated with increased induction of SA-regulated Pathogenesis-Related 1 (PR1) by the bacterial pathogen. Transgenic plants that constitutively overexpress WRKY7 have altered leaf growth and morphology strikingly similar to those observed in the previously isolated eds8 mutant plants. Like eds8 mutant plants, WRKY7-overexpressing plants supported more growth of P. syringae and developed more severe disease symptoms than wild-type plants. The enhanced susceptibility of both the WRKY7-overexpressing plants and the eds8 mutant correlated with reduced expression of defense-related genes, including PR1, but significantly increased accumulation of SA after pathogen infection, probably due to reduced negative feedback of SA synthesis. Thus, pathogen-induced WRKY7 transcription factor play a negative role in defense responses to P. syringae.
拟南芥(Arabidopsis thaliana)的WRKY7基因受病原体感染和水杨酸(SA)处理诱导,因此可能在植物防御反应中发挥作用。在此,我们表明WRKY7定位于细胞核,识别含有W盒(TTGAC)元件的DNA分子,并在植物细胞中作为转录抑制因子发挥作用。为了直接研究其生物学功能,我们对拟南芥中WRKY7的功能缺失型T-DNA插入突变体和RNA干扰突变体以及功能获得型转基因过表达植株进行了表征。通过测量细菌生长和症状发展与野生型植株相比显著降低,发现T-DNA插入突变体和RNA干扰突变体植株对细菌性病原体丁香假单胞菌的强毒株表现出增强的抗性。功能缺失突变体中增强的抗性与细菌病原体对SA调节的病程相关蛋白1(PR1)诱导增加有关。组成型过表达WRKY7的转基因植株叶片生长和形态发生改变,与之前分离的eds8突变体植株中观察到的情况极为相似。与eds8突变体植株一样,过表达WRKY7的植株比野生型植株支持丁香假单胞菌更多的生长,并表现出更严重的病害症状。过表达WRKY7的植株和eds8突变体增强的易感性与防御相关基因(包括PR1)表达降低相关,但病原体感染后SA积累显著增加,这可能是由于SA合成的负反馈减少所致。因此,病原体诱导的WRKY7转录因子在对丁香假单胞菌的防御反应中起负作用。