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首页> 外文期刊>Molecular Plant-Microbe Interactions >Induction of the Hahsp17.7G4 Promoter by Root-Knot Nematodes: Involvement of Heat-Shock Elements in Promoter Activity in Giant Cells
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Induction of the Hahsp17.7G4 Promoter by Root-Knot Nematodes: Involvement of Heat-Shock Elements in Promoter Activity in Giant Cells

机译:根结线虫诱导Hahsp17.7G4启动子:热休克因子参与巨细胞启动子活性。

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Root-knot nematodes feed from specialized giant cells induced in the plants that they parasitize. We found that the promoter of the Hahsp17.7G4 gene, which encodes a small heat-shock protein involved in embryogenesis and stress responses, directed GUS expression in tobacco galls induced by the root-knot nematode Meloidogyne incognita . In roots containing a GUS reporter fusion to the Hahsp17.7G4 promoter, 10% of the galls stained for GUS expression 1 to 3 days after infection and the fraction stained increased to 60 to 80% 17 to 20 days after infection. A DNA fragment from ?83 to +163, which contains heat-shock element (HSE) core sequences, is sufficient to support a promoter activity largely restricted to giant cells within the galls. Two-point mutations in HSE cores, previously reported to abolish the heat-shock response and to strongly reduce the embryogenesis response of the same promoter, did not reduce expression in giant cells. This suggests a distinct regulation of the promoter by nematodes. However, additional point mutations located at positions crucial for binding of heat-shock transcription factors (HSFs) caused a severe decrease in the nematode response. These results demonstrate that HSEs are involved in the promoter activation in giant cells and suggest that HSFs may mediate this response.
机译:根结线虫以寄生于植物中的特化巨型细胞为食。我们发现,Hahsp17.7G4基因的启动子编码参与胚胎发生和应激反应的小热休克蛋白,指导根结线虫Meloidogyne incognita诱导的烟gall中的GUS表达。在含有与Hahsp17.7G4启动子融合的GUS报告基因的根中,感染后1到3天将10%的胆汁染色以显示GUS表达,感染后17到20天染色的比例增加到60%到80%。包含热休克元件(HSE)核心序列的〜83至+163的DNA片段足以支持启动子活性,该启动子活性主要限于胆囊内的巨细胞。 HSE核心中的两点突变以前没有报道消除热激反应,并强烈降低了同一启动子的胚胎发生反应,但并未减少巨细胞中的表达。这表明线虫对启动子的独特调节。但是,位于对热休克转录因子(HSFs)结合至关重要的位置的其他点突变导致线虫反应严重降低。这些结果表明,HSE与巨细胞的启动子激活有关,并暗示HSF可以介导这种反应。

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