首页> 美国卫生研究院文献>The Journal of Biological Chemistry >A Novel WRKY-like Protein Involved in Transcriptional Activation of Cyst Wall Protein Genes in Giardia lamblia
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A Novel WRKY-like Protein Involved in Transcriptional Activation of Cyst Wall Protein Genes in Giardia lamblia

机译:一种新型的WRKY样蛋白参与了贾第鞭毛虫囊壁蛋白基因的转录激活。

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摘要

Synthesis of a protective cyst wall is required for survival outside of the host and for infection of Giardia lamblia. Little is known of gene regulation of the cyst wall proteins (CWPs) during differentiation into dormant cysts. WRKY homologues constitute a large family of DNA-binding proteins in plants that are involved in several key cellular functions, including disease resistance, stress response, dormancy, and development. A putative wrky gene has been identified in the G. lamblia genome. We found that wrky expression levels increased significantly during encystation. The epitope-tagged WRKY was translocated into the nuclei during encystation. Recombinant WRKY specifically bound to its own promoter and the encystation-induced cwp1 and cwp2 promoters. WRKY contains several key residues for DNA binding, and mutation analysis revealed that its binding sequences are similar to those of the known plant WRKY proteins and that two of them are positive cis-acting elements of the wrky and cwp2 promoters. Overexpression of WRKY increased the cwp1-2 and myb2 mRNA levels, and these gene promoters were bound by WRKY in vivo. Interestingly, the wrky and cwp1-2 genes were up-regulated by ERK1 (extracellular signal-related kinase 1) overexpression, suggesting that WRKY may be a downstream component of the ERK1 pathway. In addition, a WRKY mutant that cannot enter nuclei and an ERK1 mutant lacking the predicted kinase domain showed decreased cwp1-2 gene expression. Our results suggest that the WRKY family has been conserved during evolution and that WRKY is an important transactivator of the cwp1-2 genes during G. lamblia differentiation into dormant cysts.
机译:需要合成保护性囊肿壁才能在宿主体外存活和感染贾第鞭毛虫。分化为休眠性囊肿期间对囊壁蛋白(CWP)的基因调控了解甚少。 WRKY同源物在植物中构成了一个大家族的DNA结合蛋白,这些蛋白与几种关键的细胞功能有关,包括抗病性,胁迫反应,休眠和发育。在兰伯氏菌基因组中已经鉴定出一个推定的变态基因。我们发现在融合过程中,异常的表达水平显着增加。带有抗原决定簇的WRKY在融合过程中被转移到细胞核中。重组WRKY特异地结合到其自身的启动子以及ongstation诱导的cwp1和cwp2启动子。 WRKY包含几个与DNA结合的关键残基,突变分析表明其结合序列与已知植物WRKY蛋白的结合序列相似,并且其中两个是wrky和cwp2启动子的正顺式作用元件。 WRKY的过表达增加了cwp1-2和myb2 mRNA的水平,并且这些基因启动子在体内被WRKY结合。有趣的是,wrky和cwp1-2基因被ERK1(细胞外信号相关激酶1)的过表达上调,表明WRKY可能是ERK1途径的下游成分。此外,无法进入细胞核的WRKY突变体和缺少预测的激酶结构域的ERK1突变体显示cwp1-2基因表达降低。我们的结果表明WRKY家族在进化过程中一直处于保守状态,并且WRKY是 G时期cwp1-2基因的重要反式激活因子。羊羔分化为休眠性囊肿。

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