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Functional analysis of Arabidopsis WRKY25 transcription factor in plant defense against Pseudomonas syringae

机译:拟南芥WRKY25转录因子在植物抗丁香假单胞菌中的功能分析

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Background A common feature of plant defense responses is the transcriptional regulation of a large number of genes upon pathogen infection or treatment with pathogen elicitors. A large body of evidence suggests that plant WRKY transcription factors are involved in plant defense including transcriptional regulation of plant host genes in response to pathogen infection. However, there is only limited information about the roles of specific WRKY DNA-binding transcription factors in plant defense. Results We analyzed the role of the WRKY25 transcription factor from Arabidopsis in plant defense against the bacterial pathogen Pseudomonas syringae . WRKY25 protein recognizes the TTGACC W-box sequences and its translational fusion with green fluorescent protein is localized to the nucleus. WRKY25 expression is responsive to general environmental stress. Analysis of stress-induced WRKY25 in the defense signaling mutants npr1 , sid2 , ein2 and coi1 further indicated that this gene is positively regulated by the salicylic acid (SA) signaling pathway and negatively regulated by the jasmonic acid signaling pathway. Two independent T-DNA insertion mutants for WRKY25 supported normal growth of a virulent strain of P. syringae but developed reduced disease symptoms after infection. By contrast, Arabidopsis constitutively overexpressing WRKY25 supported enhanced growth of P. syringae and displayed increased disease symptom severity as compared to wild-type plants. These WRKY25 -overexpressing plants also displayed reduced expression of the SA-regulated PR1 gene after the pathogen infection, despite normal levels of free SA. Conclusion The nuclear localization and sequence-specific DNA-binding activity support that WRKY25 functions as a transcription factor. Based on analysis of both T-DNA insertion mutants and transgenic overexpression lines, stress-induced WRKY25 functions as a negative regulator of SA-mediated defense responses to P. syringae . This proposed role is consistent with the recent finding that WRKY25 is a substrate of Arabidopsis MAP kinase 4, a repressor of SA-dependent defense responses.
机译:背景技术植物防御反应的共同特征是在病原体感染或用病原体引发剂处理后大量基因的转录调控。大量证据表明植物WRKY转录因子参与植物防御,包括响应病原体感染的植物宿主基因转录调控。但是,关于特定的WRKY DNA结合转录因子在植物防御中的作用的信息很少。结果我们分析了拟南芥中WRKY25转录因子在植物抵抗丁香假单胞菌中的作用。 WRKY25蛋白可识别TTGACC W-box序列,其与绿色荧光蛋白的翻译融合位于细胞核。 WRKY25表达对一般环境压力有反应。分析防御信号突变体npr1,sid2,ein2和coi1中的应激诱导的WRKY25进一步表明,该基因受水杨酸(SA)信号传导途径正调控,而茉莉酸信号途径却受负调控。 WRKY25的两个独立的T-DNA插入突变体支持丁香假单胞菌强毒株的正常生长,但感染后疾病症状减轻。相比之下,与野生型植物相比,组成型过表达WRKY25的拟南芥支持丁香假单胞菌的生长增强,并显示出增加的疾病症状严重性。尽管游离SA水平正常,但这些WRKY25过表达植物在病原体感染后也显示出SA调节的PR1基因表达降低。结论核定位和序列特异性DNA结合活性支持WRKY25作为转录因子。基于对T-DNA插入突变体和转基因过表达株系的分析,应激诱导的WRKY25充当SA介导的对丁香假单胞菌的防御反应的负调节剂。拟议的作用与最近的发现一致,即WRKY25是拟南芥MAP激酶4的底物,拟南芥MAP激酶4是SA依赖性防御反应的阻遏物。

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