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Overlap of Promoter Recognition Specificity of Stress Response Sigma Factors SigD and SigH in Corynebacterium glutamicum ATCC 13032

机译:谷氨酸棒杆菌ATCC 13032中应激反应西格玛因子SigD和SigH的启动子识别特异性的重叠。

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摘要

Corynebacterium glutamicum ATCC 13032 harbors five sigma subunits of RNA polymerase belonging to Group IV, also called extracytoplasmic function (ECF) σ factors. These factors σC, σD, σE, σH, and σM are mostly involved in stress responses. The role of σD consists in the control of cell wall integrity. The σD regulon is involved in the synthesis of components of the mycomembrane which is part of the cell wall in C. glutamicum. RNA sequencing of the transcriptome from a strain overexpressing the sigD gene provided 29 potential σD-controlled genes and enabled us to precisely localize their transcriptional start sites. Analysis of the respective promoters by both in vitro transcription and the in vivo two-plasmid assay confirmed that transcription of 11 of the tested genes is directly σD-dependent. The key sequence elements of all these promoters were found to be identical or closely similar to the motifs -35 GTAACA/G and -10 GAT. Surprisingly, nearly all of these σD-dependent promoters were also active to a much lower extent with σH in vivo and one (Pcg0607) also in vitro, although the known highly conserved consensus sequence of the σH-dependent promoters is different (-35 GGAAT/C and -10 GTT). In addition to the activity of σH at the σD-controlled promoters, we discovered separated or overlapping σA- or σB-regulated or σH-regulated promoters within the upstream region of 8 genes of the σD-regulon. We found that phenol in the cultivation medium acts as a stress factor inducing expression of some σD-dependent genes. Computer modeling revealed that σH binds to the promoter DNA in a similar manner as σD to the analogous promoter elements. The homology models together with mutational analysis showed that the key amino acids, Ala 60 in σD and Lys 53 in σH, bind to the second nucleotide within the respective -10 promoter elements (G>AT and G>TT, respectively). The presented data obtained by integrating in vivo, in vitro and in silico approaches demonstrate that most of the σD-controlled genes also belong to the σH-regulon and are also transcribed from the overlapping or closely located housekeeping (σA-regulated) and/or general stress (σB-regulated) promoters.
机译:谷氨酸棒杆菌ATCC 13032包含属于IV组的五个RNA聚合酶的sigma亚基,也称为胞浆外功能(ECF)σ因子。这些因素σ C ,σ D ,σ E ,σ H 和σ M 主要参与压力反应。 σ D 的作用在于细胞壁完整性的控制。 σ D 调节子参与了肌膜成分的合成,该膜是谷氨酸棒杆菌细胞壁的一部分。过量表达sigD基因的菌株转录组的RNA测序提供了29个潜在的σ D 控制基因,使我们能够精确定位其转录起始位点。通过体外转录和体内双质粒试验对各个启动子的分析证实,所测试基因中的11个的转录直接依赖于σ D 。发现所有这些启动子的关键序列元件与-35 GTAAC A / G和-10 GAT基序相同或非常相似。出乎意料的是,几乎所有这些依赖于σ D 的启动子在体内对σ H 的活性也都低得多,尽管在体外也有一个(Pcg0607)活性。 σ H 依赖性启动子的高度保守共有序列不同(-35 GGAA T / C和-10 GTT)。除了在σ D 控制的启动子上σ H 的活性外,我们还发现了分离或重叠的σ A -或σ在s D -调节子的8个基因的上游区域中,B 调控或σ H 调控的启动子。我们发现培养基中的苯酚是诱导某些σ D 依赖基因表达的应激因子。计算机建模表明,σ H 以与σ D 类似的方式与启动子DNA结合。同源性模型和突变分析表明,关键氨基酸σ D 中的Ala 60和σ H 中的Lys 53与各自-10中的第二个核苷酸结合启动子元素(分别为G > A T和G > T T)。通过整合体内,体外和计算机方法获得的数据表明,大多数受σ D 控制的基因也属于σ H -调节子,并且从重叠或位置接近的客房服务(σ A 调节)和/或普通压力(σ B 调节)启动子转录。

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