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Molecular and genetic studies of Fusarium trichothecene biosynthesis: toward understanding the transcriptional regulatory mechanisms of trichothecene (Tri) genes

机译:镰刀菌的分子和遗传研究生物合成:朝向理解三胞素(三)基因的转录调节机制

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To gain insights into the regulatory mechanism of trichothecene biosynthesis, I worked on molecular genetic studies of Fusarium graminearum in RIKEN and Nagoya University. First, Aspergillus nldulans promoters with different levels of transcription were identified and characterized in F. gramienarum. Second, subcellular localization of Tri6p, a zinc finger protein essential for trichothecene (Tri) gene transcription, was analyzed by using these promoters. When the predicted nuclear localization sequence (NLS) of Tri6 was fused to the EGFP (enhanced green fluorescence protein) gene and transcribed under the control of a strong A. nidulans TEFla promoter, the EGFP green fluorescence was clearly observed in the nucleus, demonstrating the functionalityof the nuclear localization signal. Third, the role of sucrose as an inducer, but not as the carbon source of the medium, in trichothecene production was unambiguously demonstrated. Based on the mode of actions of sucrose and other chemicals that modulate trichothecene production, a new regulatory model of Tri6 expression is now being proposed. Further investigations with molecular and mechanisms of genetic approaches using these tools will clarify the trichothecene biosynthesis regulation.
机译:为了进入三胞素生物合成的监管机制,我研究了瑞肯和名古屋大学富疮素雷诺姆的分子遗传研究。首先,鉴定具有不同转录水平的曲霉菌胰岛素促进剂并表征F. Gramianarum。其次,通过使用这些启动子分析TRI6P的亚细胞定位,TRI6P,对三胞内癸烯(TRI)基因转录的锌指蛋白质是必不可少的。当TRI6的预测核定位序列(NLS)与EGFP(增强的绿色荧光蛋白)基因融合并在强的A.Nidulans Tefla启动子的控制下转录时,在核中清楚地观察到EGFP绿色荧光,证明了核定位信号的功能。第三,蔗糖作为诱导剂的作用,但不是培养基的碳源,在三胞内癸烯生产中明确证明。基于调节Trichothecene生产的蔗糖和其他化学品的作用方式,现在提出了一种新的TRI6表达调控模型。利用这些工具的分子和遗传方法的进一步调查将阐明Trichothecene生物合成调控。

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