首页> 外文期刊>Molecular Microbiology >The developmental regulator MtrA binds GlnR boxes and represses nitrogen metabolism genes in Streptomyces coelicolor Streptomyces coelicolor
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The developmental regulator MtrA binds GlnR boxes and represses nitrogen metabolism genes in Streptomyces coelicolor Streptomyces coelicolor

机译:发育调节剂MTRA结合GLNR盒并抑制链霉菌的氮霉菌链霉菌链霉菌的氮素代谢基因

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摘要

Summary In Streptomyces , GlnR is an activator protein that activates nitrogen‐assimilation genes under nitrogen‐limiting conditions. However, less is known regarding the regulation of these genes under nitrogen‐rich conditions. We determined that the developmental regulator MtrA represses nitrogen‐assimilation genes in nitrogen‐rich media and that it competes with GlnR for binding to GlnR boxes. The GlnR boxes upstream of multiple nitrogen genes, such as amtB , were confirmed as MtrA binding sites in vitro by electrophoretic mobility shift assays and in vivo by ChIP‐qPCR analysis. Transcriptional analysis indicated that, on nutrient‐rich medium, MtrA profoundly repressed expression of nitrogen‐associated genes, indicating opposing roles for MtrA and GlnR in the control of nitrogen metabolism. Using in vitro and in vivo analysis, we also showed that glnR is itself a direct target of MtrA and that MtrA represses glnR transcription. We further demonstrated functional conservation of MtrA homologues in the recognition of GlnR boxes upstream of nitrogen genes from different actinobacterial species. As mtrA and glnR are widespread among actinomycetes, this mechanism of potential competitive control over nitrogen metabolism genes may be common in this group, adding a major new layer of complexity to the known regulatory network for nitrogen metabolism in Streptomyces and related species.
机译:发明概述在链霉菌中,GLNR是一种活化剂蛋白,其在氮气限制条件下激活氮氧化基因。然而,在富含氮的条件下对这些基因的调节较少。我们确定发育调节剂MTRA在富含氮培养基中抑制氮同化基因,并且它与GLNR竞争结合GLNR盒。通过电泳迁移率移位测定和通过芯片-QPCR分析,通过电泳迁移率移位和体内确认多个氮基因(例如AMTB)上游的GLNR盒作为MTRA结合位点确认为MTRA结合位点。转录分析表明,在富含营养素的培养基上,MTRA深受氮相关基因的表达,表明MTRA和GLNR在控制氮代谢中的相反作用。在体外和体内分析中使用,我们还表明GLNR本身是MTRA的直接目标,并且MTRA抑制GLNR转录。我们进一步证明了MTRA同源物的功能守恒,以识别来自不同肌动杆菌物种的氮基因上游的GLNR盒。作为MTRA和glnR是放线菌的广泛,在氮代谢基因的潜在竞争力的控制的这种机制可能是本组中常见的,增加了复杂性的一个重要的新层,已知的监管网络,在链霉菌及相关品种氮代谢。

著录项

  • 来源
    《Molecular Microbiology》 |2019年第1期|共18页
  • 作者单位

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial MetabolismShanghai Jiao Tong UniversityShanghai 200240 China;

    Shandong Medicinal Biotechnology CenterShandong Academy of Medical SciencesJinan 250062 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    College of Life SciencesShanghai Normal UniversityShanghai 200232 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

    The State Key Laboratory of Microbial TechnologyShandong UniversityQingdao 266237 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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