Wassem Roseli, Kobayashi Hajime, Kambara Kumiko, Le Quéré Antoine, Walker Graham C, Broughton William J, Deakin William J
Laboratoire de Biologie Moléculaire des Plantes Supérieures, Sciences III, 30 Quai Ernest-Ansermet, Université de Genève, CH-1211 Geneva 4, Switzerland.
Mol Microbiol. 2008 May;68(3):736-48. doi: 10.1111/j.1365-2958.2008.06187.x. Epub 2008 Mar 20.
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.
根瘤菌NGR234对豆科植物的侵染以及随后固氮根瘤的形成依赖于结瘤因子、III型分泌系统(T3SS)分泌的蛋白质以及表面多糖修饰的协同作用。这些信号分子的产生依赖于植物黄酮类化合物,其触发由转录激活因子NodD1、NodD2、SyrM2和TtsI控制的调控级联反应。已知TtsI控制负责T3SS功能和合成具有共生重要性的富含鼠李糖的脂多糖的基因,很可能是通过与称为tts框的顺式元件结合来实现的。在NGR234共生质粒上靶基因的启动子区域中鉴定出11个tts框。与这些tts框的lacZ融合表达谱表明,它们是由植物来源的黄酮类化合物诱导的TtsI依赖性调节子的一部分。TtsI被纯化,并证明可直接与其中两个tts框结合。DNase I足迹分析表明,TtsI不仅占据tts框共有序列,还以浓度依赖的方式占据上游和下游区域。共有tts框的高度保守碱基发生了突变,尽管在体外仍观察到TtsI结合,但gfp融合在体内不再转录。对含有tts框的启动子进行随机诱变,发现在共有序列之外还有更多对转录活性至关重要的核苷酸。