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首页> 外文期刊>Functional & integrative genomics >The transcriptional network of WRKY53 in cereals links oxidative responses to biotic and abiotic stress inputs
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The transcriptional network of WRKY53 in cereals links oxidative responses to biotic and abiotic stress inputs

机译:谷物中WRKY53的转录网络将氧化反应与生物和非生物胁迫输入联系起来

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摘要

The transcription factor WRKY53 is expressed during biotic and abiotic stress responses in cereals, but little is currently known about its regulation, structure and downstream targets. We sequenced the wheat ortholog TaWRKY53 and its promoter region, which revealed extensive similarity in gene architecture and cis-acting regulatory elements to the rice ortholog OsWRKY53, including the presence of stressresponsive abscisic acid-responsive elements (ABRE) motifs and GCC-boxes. Four proteins interacted with the WRKY53 promoter in yeast one-hybrid assays, suggesting that this gene can receive inputs from diverse stress-related pathways such as calcium signalling and senescence, and environmental cues such as drought and ultraviolet radiation. The Ser/Thr receptor kinase ORK10/LRK10 and the apoplastic peroxidase POC1 are two downstream targets for regulation by the WRKY53 transcription factor, predicted based on the presence ofW-box motifs in their promoters and coregulation with WRKY53, and verified by electrophoretic mobility shift assay (EMSA). Both ORK10/LRK10 and POC1 are upregulated during cereal responses to pathogens and aphids and important components of the oxidative burst during the hypersensitive response. Taken with our yeast two-hybrid assay which identified a strong protein–protein interaction between microsomal glutathione S-transferase 3 and WRKY53, this implies that the WRKY53 transcriptional network regulates oxidative responses to a wide array of stresses.
机译:转录因子WRKY53在谷物的生物和非生物胁迫反应期间表达,但目前对其调控,结构和下游靶点知之甚少。我们对小麦直系同源基因TaWRKY53及其启动子区域进行了测序,该序列揭示了与大分子直系同源基因OsWRKY53在基因结构和顺式作用调控元件上的广泛相似性,包括存在应激反应的脱落酸反应元件(ABRE)图案和GCC-boxes。在酵母一杂交实验中,四种蛋白质与WRKY53启动子相互作用,这表明该基因可以从多种与压力相关的途径(如钙信号传导和衰老)以及环境提示(如干旱和紫外线辐射)中接受输入。 Ser / Thr受体激酶ORK10 / LRK10和质外体过氧化物酶POC1是WRKY53转录因子调控的两个下游靶标,根据其启动子中W-box基序的存在预测并与WRKY53共调节,并通过电泳迁移率漂移分析进行验证(EMSA)。谷类对病原体和蚜虫的反应以及超敏反应过程中氧化爆发的重要组成部分均会上调ORK10 / LRK10和POC1。与我们的酵母双杂交测定法一起使用,该测定法确定了微粒体谷胱甘肽S-转移酶3和WRKY53之间的强蛋白-蛋白相互作用,这表明WRKY53转录网络调节了对多种应激的氧化反应。

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