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鉴定和特性分析腾格里沙漠嗜热菌 ECFσ 因子的同源抗σ 因子和特异启动子元件。

Identification and characterization of the cognate anti-sigma factor and specific promoter elements of a T. tengcongensis ECF sigma factor.

机构信息

State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, People's Republic of China.

出版信息

PLoS One. 2012;7(7):e40885. doi: 10.1371/journal.pone.0040885. Epub 2012 Jul 16.

Abstract

Extracytoplasmic function (ECF) σ factors, the largest group of alternative σ factors, play important roles in response to environmental stresses. Tt-RpoE1 is annotated as an ECF σ factor in Thermoanaerobacter tengcongensis. In this study, we revealed that the Tt-tolB gene located downstream of the Tt-rpoE1 gene encoded the cognate anti-σ factor, which could inhibit the transcription activity of Tt-RpoE1 by direct interaction with Tt-RpoE1 via its N-terminal domain. By in vitro transcription assay, the auto-regulation ability of Tt-RpoE1 was determined, and band shift assay showed that Tt-RpoE1 preferred to bind a fork-junction promoter DNA. With truncation or base-specific scanning mutations, the contribution of the nucleotides in -35 and -10 regions to interaction between Tt-RpoE1 and promoter DNA was explored. The promoter recognition pattern of Tt-RpoE1 was determined as 5' tGTTACN(16)CGTC 3', which was further confirmed by in vitro transcription assays. This result showed that the Tt-RpoE1-recognized promoter possessed a distinct -10 motif (-13CGTC-10) as the recognition determinant, which is distinguished from the -10 element recognized by σ(70). Site-directed mutagenesis in Region 2.4 of Tt-RpoE1 indicated that the "D" residue of DXXR motif was responsible for recognizing the -12G nucleotide. Our results suggested that distinct -10 motif may be an efficient and general strategy used by ECF σ factors in adaptive response regulation of the related genes.

摘要

细胞外功能 (ECF) σ 因子是最大的一类替代 σ 因子,在应对环境压力方面发挥着重要作用。Tt-RpoE1 在 Thermoanaerobacter tengcongensis 中被注释为 ECF σ 因子。在本研究中,我们揭示了位于 Tt-rpoE1 基因下游的 Tt-tolB 基因编码了与其对应的反式作用 σ 因子,该反式作用 σ 因子通过其 N 端结构域与 Tt-RpoE1 直接相互作用来抑制 Tt-RpoE1 的转录活性。通过体外转录实验确定了 Tt-RpoE1 的自我调控能力,并且迁移率变动分析表明 Tt-RpoE1 优先与分叉接头启动子 DNA 结合。通过截短或碱基特异性扫描突变,探讨了-35 和 -10 区域的核苷酸对 Tt-RpoE1 与启动子 DNA 相互作用的贡献。确定了 Tt-RpoE1 的启动子识别模式为 5' tGTTACN(16)CGTC 3',这一结果通过体外转录实验得到进一步证实。结果表明,Tt-RpoE1 识别的启动子具有独特的-10 基序 (-13CGTC-10) 作为识别决定簇,这与 σ(70) 识别的-10 元件不同。Tt-RpoE1 区域 2.4 中的定点突变表明,DXXR 基序中的“D”残基负责识别-12G 核苷酸。我们的结果表明,独特的-10 基序可能是 ECF σ 因子在相关基因适应性反应调节中使用的一种有效且通用的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f93f/3397946/caaa3e341eda/pone.0040885.g001.jpg

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