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水稻感病基因的启动子元件被来自细菌性条斑病菌的特异 TAL 效应因子结合并激活,该病菌是水稻白叶枯病菌。

Promoter elements of rice susceptibility genes are bound and activated by specific TAL effectors from the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae.

机构信息

Institute of Biology, Martin-Luther-University Halle-Wittenberg, 06099 Halle (Saale), Germany.

Present address: Institute of Genetics, University of Munich (LMU), Großhaderner Straße 2, 82152 Martinsried, Germany.

出版信息

New Phytol. 2010 Sep;187(4):1048-1057. doi: 10.1111/j.1469-8137.2010.03217.x. Epub 2010 Mar 19.

Abstract

*Plant pathogenic bacteria of the genus Xanthomonas inject transcription activator-like effector (TALe) proteins that bind to and activate host promoters, thereby promoting disease or inducing plant defense. TALes bind to corresponding UPT (up-regulated by TALe) promoter boxes via tandemly arranged 34/35-amino acid repeats. Recent studies uncovered the TALe code in which two amino acid residues of each repeat define specific pairing to UPT boxes. *Here we employed the TALe code to predict potential UPT boxes in TALe-induced host promoters and analyzed these via beta-glucuronidase (GUS) reporter and electrophoretic mobility shift assays (EMSA). *We demonstrate that the Xa13, OsTFX1 and Os11N3 promoters from rice are induced directly by the Xanthomonas oryzae pv. oryzae TALes PthXo1, PthXo6 and AvrXa7, respectively. We identified and functionally validated a UPT box in the corresponding rice target promoter for each TALe and show that box mutations suppress TALe-mediated promoter activation. Finally, EMSA demonstrate that code-predicted UPT boxes interact specifically with corresponding TALes. *Our findings show that variations in the UPT boxes of different rice accessions correlate with susceptibility or resistance of these accessions to the bacterial blight pathogen.

摘要

植物病原细菌黄单胞菌属注射转录激活子样效应物(TALe)蛋白,这些蛋白与宿主启动子结合并激活,从而促进疾病或诱导植物防御。TALes 通过串联排列的 34/35 个氨基酸重复序列结合到相应的 UPT(TALe 上调)启动子盒上。最近的研究揭示了 TALe 密码,其中每个重复的两个氨基酸残基定义了与 UPT 盒的特定配对。在这里,我们利用 TALe 密码来预测 TALe 诱导的宿主启动子中的潜在 UPT 盒,并通过β-葡萄糖醛酸酶(GUS)报告基因和电泳迁移率变动分析(EMSA)对其进行分析。我们证明,来自水稻的 Xa13、OsTFX1 和 Os11N3 启动子分别被水稻黄单胞菌 pv.oryzae 的 TALes PthXo1、PthXo6 和 AvrXa7 直接诱导。我们鉴定并功能验证了每个 TALe 对应的水稻靶启动子中的 UPT 盒,并表明框突变抑制了 TALe 介导的启动子激活。最后,EMSA 表明,预测密码的 UPT 框与相应的 TALe 特异性相互作用。我们的研究结果表明,不同水稻品系的 UPT 盒的变异与这些品系对细菌性条斑病病原体的敏感性或抗性相关。

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