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本文引用的文献

1
Nucleotide-dependent interactions between a fork junction-RNA polymerase complex and an AAA+ transcriptional activator protein.叉状连接-RNA聚合酶复合物与AAA+转录激活蛋白之间的核苷酸依赖性相互作用。
Nucleic Acids Res. 2004 Aug 27;32(15):4596-608. doi: 10.1093/nar/gkh755. Print 2004.
2
Purification and characterization of the AAA+ domain of Sinorhizobium meliloti DctD, a sigma54-dependent transcriptional activator.苜蓿中华根瘤菌DctD(一种依赖σ54的转录激活因子)的AAA+结构域的纯化与鉴定
J Bacteriol. 2004 Jun;186(11):3499-507. doi: 10.1128/JB.186.11.3499-3507.2004.
3
Structural basis of transcription: an RNA polymerase II-TFIIB cocrystal at 4.5 Angstroms.转录的结构基础:4.5埃分辨率下的RNA聚合酶II-TFIIB共晶体结构
Science. 2004 Feb 13;303(5660):983-8. doi: 10.1126/science.1090838.
4
Roles for inhibitory interactions in the use of the -10 promoter element by sigma 70 holoenzyme.抑制性相互作用在σ70全酶对-10启动子元件的利用中的作用。
J Biol Chem. 2003 Oct 10;278(41):39669-74. doi: 10.1074/jbc.M307412200. Epub 2003 Aug 4.
5
Mapping sigma 54-RNA polymerase interactions at the -24 consensus promoter element.绘制σ54 - RNA聚合酶在 - 24共有启动子元件处的相互作用图谱。
J Biol Chem. 2003 Aug 8;278(32):29728-43. doi: 10.1074/jbc.M303596200. Epub 2003 May 15.
6
Nucleotide-dependent triggering of RNA polymerase-DNA interactions by an AAA regulator of transcription.转录的AAA调节因子对RNA聚合酶与DNA相互作用的核苷酸依赖性触发。
J Biol Chem. 2003 May 30;278(22):19815-25. doi: 10.1074/jbc.M301296200. Epub 2003 Mar 20.
7
The sigma70 family of sigma factors.σ因子的σ70家族。
Genome Biol. 2003;4(1):203. doi: 10.1186/gb-2003-4-1-203. Epub 2003 Jan 3.
8
Multiple roles of the RNA polymerase beta subunit flap domain in sigma 54-dependent transcription.RNA聚合酶β亚基侧翼结构域在σ⁵⁴依赖转录中的多种作用
J Biol Chem. 2003 Jan 31;278(5):3455-65. doi: 10.1074/jbc.M209442200. Epub 2002 Nov 6.
9
Mechanochemical ATPases and transcriptional activation.机械化学ATP酶与转录激活
Mol Microbiol. 2002 Aug;45(4):895-903. doi: 10.1046/j.1365-2958.2002.03065.x.
10
The downstream DNA jaw of bacterial RNA polymerase facilitates both transcriptional initiation and pausing.细菌RNA聚合酶的下游DNA钳口有助于转录起始和暂停。
J Biol Chem. 2002 Oct 4;277(40):37456-63. doi: 10.1074/jbc.M207038200. Epub 2002 Jul 29.

为使DNA解链而对RNA聚合酶-启动子DNA复合物进行的重组。

Reorganisation of an RNA polymerase-promoter DNA complex for DNA melting.

作者信息

Burrows Patricia C, Severinov Konstantin, Buck Martin, Wigneshweraraj Siva R

机构信息

Department of Biological Sciences, Imperial College London, London SW7 2AZ, UK.

出版信息

EMBO J. 2004 Oct 27;23(21):4253-63. doi: 10.1038/sj.emboj.7600406. Epub 2004 Oct 7.

DOI:10.1038/sj.emboj.7600406
PMID:15470504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC524386/
Abstract

Sigma factors, the key regulatory components of the bacterial RNA polymerase (RNAP), direct promoter DNA binding and DNA melting. The sigma(54)-RNAP forms promoter complexes in which DNA melting is only triggered by an activator and ATP hydrolysis-driven reorganisation of an initial sigma(54)-RNAP-promoter complex. We report that an initial bacterial RNAP-DNA complex can be reorganised by an activator to form an intermediate transcription initiation complex where full DNA melting has not yet occurred. Using sigma(54) as a chemical nuclease we now show that the reorganisation of the initial sigma(54)-RNAP-promoter complex occurs upon interaction with the activator at the transition point of ATP hydrolysis. We demonstrate that this reorganisation event is an early step in the transcription initiation pathway that occurs independently of RNAP parts normally associated with stable DNA melting and open complex formation. Using photoreactive DNA probes, we provide evidence that within this reorganised sigma(54)-RNAP-promoter complex, DNA contacts across the 'to be melted' sequences are made by the sigma(54) subunit. Strikingly, the activator protein, but not core RNAP subunits, is close to these DNA sequences.

摘要

σ因子是细菌RNA聚合酶(RNAP)的关键调控成分,负责指导启动子DNA结合和DNA解链。σ⁵⁴-RNAP形成启动子复合物,其中DNA解链仅由激活剂以及ATP水解驱动的初始σ⁵⁴-RNAP-启动子复合物重排触发。我们报道,初始细菌RNAP-DNA复合物可被激活剂重排,形成尚未发生完全DNA解链的中间转录起始复合物。现在我们利用σ⁵⁴作为化学核酸酶表明,初始σ⁵⁴-RNAP-启动子复合物的重排在ATP水解的过渡点与激活剂相互作用时发生。我们证明,这种重排事件是转录起始途径中的早期步骤,其发生独立于通常与稳定DNA解链和开放复合物形成相关的RNAP部分。使用光反应性DNA探针,我们提供证据表明,在这种重排的σ⁵⁴-RNAP-启动子复合物中,“待解链”序列上的DNA接触是由σ⁵⁴亚基进行的。引人注目的是,激活蛋白而非核心RNAP亚基靠近这些DNA序列。