Centrum für Biotechnologie, Universität Bielefeld, 33594, Bielefeld, Germany.
BMC Genomics. 2012 Sep 3;13:445. doi: 10.1186/1471-2164-13-445.
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.
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.
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.
谷氨酸棒状杆菌是一种革兰氏阳性非致病性细菌,主要用于工业生产氨基酸,其基因表达由 RNA 聚合酶的七个不同σ因子调控,包括应激响应的 ECF-σ因子 SigH。sigH 基因位于一个基因簇中,与 rshA 基因一起,推测编码反σ因子。本研究的目的是分析 sigH 和 rshA 基因簇的转录调控以及 RshA 对 SigH 调控组的影响,以完善描述 SigH 和 RshA 在应激反应中的作用的模型。
转录分析表明,sigH 基因和 rshA 基因在谷氨酸棒状杆菌中由四个 sigH 组成型启动子共同转录。此外,发现一个 SigH 控制的 rshA 启动子仅驱动 rshA 基因的转录。为了在正常生长条件下测试假定的反σ因子基因 rshA 的作用,构建了谷氨酸棒状杆菌 rshA 缺失菌株,并使用 DNA 微阵列进行全基因组转录谱分析。总共,在 rshA 缺失突变体中,与亲本菌株相比,61 个假定转录单元中的 83 个基因的转录水平增加,包括使用 sigH 突变菌株检测到的基因。与二硫键应激反应、热应激蛋白、DNA 损伤的 SOS 反应组件和蛋白酶体组件相关的编码蛋白的基因是最显著上调的基因群。总共确定了鉴定基因上游的六个 SigH 依赖性启动子,并构建了由 45 个原始启动子序列组成的改良一致启动子。
rshA 基因编码一种反σ因子,控制谷氨酸棒状杆菌中应激响应的 σ 因子 SigH 的功能。从 SigH 依赖性启动子转录 rshA 可能有助于在细胞克服应激条件后快速关闭 SigH 依赖性应激反应。在这里,我们提出了一个包括 SigH、RshA 和硫氧还蛋白系统的氧化和热应激反应以及氧化还原稳态的调控模型。