首页> 外文期刊>BMC Genomics >Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
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Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum

机译:谷氨酸棒杆菌中编码应激反应性ECF西格玛因子SigH及其抗西格玛因子RshA的操纵子的转录调控及其调控网络的控制

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Background The expression of genes in Corynebacterium glutamicum, a Gram-positive non-pathogenic bacterium used mainly for the industrial production of amino acids, is regulated by seven different sigma factors of RNA polymerase, including the stress-responsive ECF-sigma factor SigH. The sigH gene is located in a gene cluster together with the rshA gene, putatively encoding an anti-sigma factor. The aim of this study was to analyze the transcriptional regulation of the sigH and rshA gene cluster and the effects of RshA on the SigH regulon, in order to refine the model describing the role of SigH and RshA during stress response. Results Transcription analyses revealed that the sigH gene and rshA gene are cotranscribed from four sigH housekeeping promoters in C. glutamicum. In addition, a SigH-controlled rshA promoter was found to only drive the transcription of the rshA gene. To test the role of the putative anti-sigma factor gene rshA under normal growth conditions, a C. glutamicum rshA deletion strain was constructed and used for genome-wide transcription profiling with DNA microarrays. In total, 83 genes organized in 61 putative transcriptional units, including those previously detected using sigH mutant strains, exhibited increased transcript levels in the rshA deletion mutant compared to its parental strain. The genes encoding proteins related to disulphide stress response, heat stress proteins, components of the SOS-response to DNA damage and proteasome components were the most markedly upregulated gene groups. Altogether six SigH-dependent promoters upstream of the identified genes were determined by primer extension and a refined consensus promoter consisting of 45 original promoter sequences was constructed. Conclusions The rshA gene codes for an anti-sigma factor controlling the function of the stress-responsive sigma factor SigH in C. glutamicum. Transcription of rshA from a SigH-dependent promoter may serve to quickly shutdown the SigH-dependent stress response after the cells have overcome the stress condition. Here we propose a model of the regulation of oxidative and heat stress response including redox homeostasis by SigH, RshA and the thioredoxin system.
机译:背景技术谷氨酸棒杆菌是一种革兰氏阳性非致病性细菌,主要用于氨基酸的工业生产,其基因表达受7种不同的RNA聚合酶σ因子(包括应激响应ECFσ因子SigH)的调节。 sigH基因与rshA基因一起位于基因簇中,rshA基因被推定编码抗σ因子。这项研究的目的是分析sigH和rshA基因簇的转录调控以及RshA对SigH regulon的影响,以完善描述SigH和RshA在应激反应中的作用的模型。结果转录分析表明,sigH基因和rshA基因是从谷氨酸棒杆菌中的四个sigH管家启动子共转录的。另外,发现SigH控制的rshA启动子仅驱动rshA基因的转录。为了测试推定的抗-sigma因子基因rshA在正常生长条件下的作用,构建了谷氨酸棒杆菌rshA缺失菌株,并将其用于DNA微阵列的全基因组转录谱分析。总计,以61个假定的转录单位组织的83个基因,包括先前使用sigH突变株检测到的基因,与其亲本菌株相比,在rshA缺失突变体中表现出更高的转录水平。编码与二硫键应激反应有关的蛋白质,热应激蛋白质,对DNA损伤的SOS反应成分和蛋白酶体成分的基因是最明显上调的基因组。通过引物延伸确定总共六个已鉴定基因上游的SigH依赖性启动子,并构建了由45个原始启动子序列组成的精制共有启动子。结论rshA基因编码一个反σ因子,可控制谷氨酸棒杆菌中应激反应的σ因子SigH的功能。细胞克服应激条件后,从SigH依赖型启动子转录rshA可能有助于迅速关闭SigH依赖性应激反应。在这里,我们提出了通过SigH,RshA和硫氧还蛋白系统调节氧化和热应激反应(包括氧化还原稳态)的模型。

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