首页> 外文OA文献 >Components of the Rv0081-Rv0088 Locus, Which Encodes a Predicted Formate Hydrogenlyase Complex, Are Coregulated by Rv0081, MprA, and DosR in Mycobacterium tuberculosis▿†
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Components of the Rv0081-Rv0088 Locus, Which Encodes a Predicted Formate Hydrogenlyase Complex, Are Coregulated by Rv0081, MprA, and DosR in Mycobacterium tuberculosis▿†

机译:Rv0081-Rv0088基因座的组件编码一个预测的甲酸酯加氢酶复合物,由结核分枝杆菌中的Rv0081,MprA和DosR共同调控。

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摘要

Mycobacterium tuberculosis, the etiological agent of tuberculosis, remains a significant cause of morbidity and mortality throughout the world despite a vaccine and cost-effective antibiotics. The success of this organism can be attributed, in part, to its ability to adapt to potentially harmful stress within the host and establish, maintain, and reactivate from long-term persistent infection within granulomatous structures. The DosRS-DosT/DevRS-Rv2027c, and MprAB two-component signal transduction systems have previously been implicated in aspects of persistent infection by M. tuberculosis and are known to be responsive to conditions likely to be found within the granuloma. Here, we describe initial characterization of a locus (Rv0081-Rv0088) encoding components of a predicted formate hydrogenylase enzyme complex that is directly regulated by DosR/DevR and MprA, and the product of the first gene in this operon, Rv0081. In particular, we demonstrate that Rv0081 negatively regulates its own expression and that of downstream genes by binding an inverted repeat element in its upstream region. In contrast, DosR/DevR and MprA positively regulate Rv0081 expression by binding to recognition sequences that either partially or completely overlap that recognized by Rv0081, respectively. Expression of Rv0081 initiates from two promoter elements; one promoter located downstream of the DosR/DevR binding site but overlapping the sequence recognized by both Rv0081 and MprA and another promoter downstream of the DosR/DevR, Rv0081, and MprA binding sites. Interestingly, Rv0081 represses Rv0081 and downstream determinants following activation of DosRS-DosT/DevRS-Rv2027c by nitric oxide, suggesting that expression of this locus is complex and subject to multiple levels of regulation. Based on this and other published information, a model is proposed detailing Rv0081-Rv0088 expression by these transcription factors within particular growth environments.
机译:尽管有疫苗和具有成本效益的抗生素,但结核分枝杆菌是结核病的病因,仍然是全世界发病率和死亡率的重要原因。该生物体的成功可以部分归因于其适应宿主内潜在有害压力并建立,维持肉芽肿结构内长期持续感染并从中重新激活的能力。 DosRS-DosT / DevRS-Rv2027c和MprAB两组分信号转导系统以前与结核分枝杆菌的持续感染有关,已知对肉芽肿内可能出现的状况有反应。在这里,我们描述了一个位置(Rv0081-Rv0088)的初始特征,该位置编码受DosR / DevR和MprA直接调控的预测的甲酸酯氢解酶复合物的成分,以及该操纵子中第一个基因Rv0081的产物。特别是,我们证明Rv0081通过在其上游区域结合一个反向重复元件来负调控其自身和下游基因的表达。相反,DosR / DevR和MprA通过分别与部分或完全重叠由Rv0081识别的识别序列的结合来正向调节Rv0081的表达。 Rv0081的表达从两个启动子元件开始;一个启动子位于DosR / DevR结合位点的下游,但与Rv0081和MprA识别的序列重叠,而另一个启动子位于DosR / DevR,Rv0081和MprA结合位点的下游。有趣的是,在由一氧化氮激活DosRS-DosT / DevRS-Rv2027c后,Rv0081抑制Rv0081和下游决定簇,这表明该基因座的表达很复杂,并且需要多种调控水平。基于此信息和其他已发布的信息,提出了一个模型,详细描述了特定生长环境中这些转录因子对Rv0081-Rv0088的表达。

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