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首页> 外文期刊>Molecular Microbiology >TtsI regulates symbiotic genes in Rhizobium species NGR234 by binding to tts boxes
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TtsI regulates symbiotic genes in Rhizobium species NGR234 by binding to tts boxes

机译:TtsI通过与TTS盒结合来调节根瘤菌NGR234中的共生基因

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Infection of legumes by Rhizobium sp. NGR234 and subsequent development of nitrogen-fixing nodules are dependent on the coordinated actions of Nod factors, proteins secreted by a type III secretion system (T3SS) and modifications to surface polysaccharides. The production of these signal molecules is dependent on plant flavonoids which trigger a regulatory cascade controlled by the transcriptional activators NodD1, NodD2, SyrM2 and TtsI. TtsI is known to control the genes responsible for T3SS function and synthesis of a symbiotically important rhamnose-rich lipo-polysaccharide, most probably by binding to cis elements termed tts boxes. Eleven tts boxes were identified in the promoter regions of target genes on the symbiotic plasmid of NGR234. Expression profiles of lacZ fusions to these tts boxes showed that they are part of a TtsI-dependent regulon induced by plant-derived flavonoids. TtsI was purified and demonstrated to bind directly to two of these tts boxes. DNase I footprinting revealed that TtsI occupied not only the tts box consensus sequence, but also upstream and downstream regions in a concentration-dependent manner. Highly conserved bases of the consensus tts box were mutated and, although TtsI binding was still observed in vitro, gfp fusions were no longer transcribed in vivo. Random mutagenesis of a tts box-containing promoter revealed more nucleotides critical for transcriptional activity outside of the consensus.
机译:根瘤菌感染豆类。 NGR234和固氮根瘤的后续发展取决于Nod因子,III型分泌系统(T3SS)分泌的蛋白质以及对表面多糖的修饰的协同作用。这些信号分子的产生取决于植物类黄酮,其触发由转录激活因子NodD1,NodD2,SyrM2和TtsI控制的调节级联反应。已知TtsI可控制负责T3SS功能和富含共生鼠李糖的脂多糖的合成的基因,最有可能通过与称为tts盒的顺式元件结合。在NGR234共生质粒上靶基因的启动子区域鉴定出11个tts盒。 lacZ融合蛋白与这些tts盒的表达谱表明,它们是植物来源的类黄酮诱导的TtsI依赖性调节子的一部分。纯化了TtsI,并证明其可直接结合至其中的两个tts盒。 DNase I足迹显示,TtsI不仅以浓度依赖性方式占据了tts框共有序列,而且还占据了上游和下游区域。共有tts框的高度保守的碱基发生了突变,尽管在体外仍观察到TtsI结合,但gfp融合体不再在体内转录。含有tts盒启动子的随机诱变显示,在共有序列之外,更多的核苷酸对于转录活性至关重要。

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