首页> 美国卫生研究院文献>Journal of Bacteriology >Involvement of Regulatory Interactions among Global Regulators GlxR SugR and RamA in Expression of ramA in Corynebacterium glutamicum
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Involvement of Regulatory Interactions among Global Regulators GlxR SugR and RamA in Expression of ramA in Corynebacterium glutamicum

机译:全局调节剂GlxRSugR和RamA之间的调节相互作用与谷氨酸棒杆菌中ramA表达的关系

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摘要

The central carbon metabolism genes in Corynebacterium glutamicum are under the control of a transcriptional regulatory network composed of several global regulators. It is known that the promoter region of ramA, encoding one of these regulators, interacts with its gene product, RamA, as well as with the two other regulators, GlxR and SugR, in vitro and/or in vivo. Although RamA has been confirmed to repress its own expression, the roles of GlxR and SugR in ramA expression have remained unclear. In this study, we examined the effects of GlxR binding site inactivation on expression of the ramA promoter-lacZ fusion in the genetic background of single and double deletion mutants of sugR and ramA. In the wild-type background, the ramA promoter activity was reduced to undetectable levels by the introduction of mutations into the GlxR binding site but increased by sugR deletion, indicating that GlxR and SugR function as the transcriptional activator and repressor, respectively. The marked repression of ramA promoter activity by the GlxR binding site mutations was largely compensated for by deletions of sugR and/or ramA. Furthermore, ramA promoter activity in the ramA-sugR double mutant was comparable to that in the ramA mutant but was significantly higher than that in the sugR mutant. Taken together, it is likely that the level of ramA expression is dynamically balanced by GlxR-dependent activation and repression by RamA along with SugR in response to perturbation of extracellular and/or intracellular conditions. These findings add multiple regulatory loops to the transcriptional regulatory network model in C. glutamicum.
机译:谷氨酸棒杆菌中的中央碳代谢基因处于由数种全球性调控子组成的转录调控网络的控制之下。已知在体外和/或体内,编码这些调节子之一的ramA的启动子区域与其基因产物RamA以及其他两个调节子GlxR和SugR相互作用。尽管已确认RamA抑制其自身表达,但仍不清楚GlxR和SugR在ramA表达中的作用。在这项研究中,我们在sugR和ramA单双缺失突变体的遗传背景中研究了GlxR结合位点失活对ramA启动子-lacZ融合蛋白表达的影响。在野生型背景中,通过将突变引入GlxR结合位点将ramA启动子活性降低到不可检测的水平,但通过sugR缺失而增加,表明GlxR和SugR分别充当转录激活因子和阻遏物。 G1xR结合位点突变对ramA启动子活性的显着抑制在很大程度上被sugR和/或ramA的缺失所补偿。此外,ramA- sugR 双重突变体中的ramA启动子活性与 ramA 突变体相当,但显着高于 sugR 突变体。综上所述,很可能响应于细胞外和/或细胞内条件的扰动, ramA 表达水平通过GlxR依赖性激活和RamA连同SugR的抑制而动态平衡。这些发现为 C中的转录调控网络模型增加了多个调控环。谷氨酸

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