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T7 RNA聚合酶在T7串联体连接处暂停和终止的机制:转录泡结构的局部变化驱动转录复合物结构的重大改变。

Mechanism of T7 RNAP pausing and termination at the T7 concatemer junction: a local change in transcription bubble structure drives a large change in transcription complex architecture.

作者信息

Nayak Dhananjaya, Siller Sylvester, Guo Qing, Sousa Rui

机构信息

Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.

出版信息

J Mol Biol. 2008 Feb 15;376(2):541-53. doi: 10.1016/j.jmb.2007.11.090. Epub 2007 Dec 4.

Abstract

The T7RNA polymerase (RNAP) elongation complex (EC) pauses and is destabilized at a unique 8 nucleotide (nt) sequence found at the junction of the head-to-tail concatemers of T7 genomic DNA generated during T7 DNA replication. The paused EC may recruit the T7 DNA processing machinery, which cleaves the concatemerized DNA within this 8 nt concatemer junction (CJ). Pausing of the EC at the CJ involves structural changes in both the RNAP and transcription bubble. However, these structural changes have not been fully defined, nor is it understood how the CJ sequence itself causes the EC to change its structure, to pause, and to become less stable. Here we use solution and RNAP-tethered chemical nucleases to probe the CJ transcript and changes in the EC structure as the polymerase pauses and terminates at the CJ. Together with extensive mutational scanning of regions of the polymerase that are likely to be involved in recognition of the CJ, we are able to develop a description of the events that occur as the EC transcribes through the CJ and subsequently pauses. In this process, a local change in the structure of the transcription bubble drives a large change in the architecture of the EC. This altered EC structure may then serve as the signal that recruits the processing machinery to the CJ.

摘要

T7 RNA 聚合酶(RNAP)延伸复合物(EC)在 T7 DNA 复制过程中产生的 T7 基因组 DNA 首尾相连的串联体连接处发现的一个独特的 8 核苷酸(nt)序列处暂停并变得不稳定。暂停的 EC 可能会招募 T7 DNA 加工机制,该机制会在这个 8 nt 串联体连接处(CJ)切割串联的 DNA。EC 在 CJ 处的暂停涉及 RNAP 和转录泡的结构变化。然而,这些结构变化尚未完全明确,也不清楚 CJ 序列本身是如何导致 EC 改变其结构、暂停并变得更不稳定的。在这里,我们使用溶液和 RNAP 连接的化学核酸酶来探测 CJ 转录本以及当聚合酶在 CJ 处暂停和终止时 EC 结构的变化。结合对聚合酶中可能参与识别 CJ 的区域进行广泛的突变扫描,我们能够描述当 EC 转录通过 CJ 并随后暂停时发生的事件。在这个过程中,转录泡结构的局部变化驱动了 EC 结构的重大变化。这种改变的 EC 结构然后可能作为将加工机制招募到 CJ 的信号。

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本文引用的文献

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Functional architecture of T7 RNA polymerase transcription complexes.T7 RNA聚合酶转录复合物的功能结构
J Mol Biol. 2007 Aug 10;371(2):490-500. doi: 10.1016/j.jmb.2007.05.070. Epub 2007 May 31.
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When transcription and repair meet: a complex system.转录与修复相遇时:一个复杂的系统。
Trends Genet. 2006 Aug;22(8):430-6. doi: 10.1016/j.tig.2006.06.006. Epub 2006 Jun 23.
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Leaving a mark: the many footprints of the elongating RNA polymerase II.留下印记:延伸中的RNA聚合酶II的众多足迹
Curr Opin Genet Dev. 2006 Apr;16(2):184-90. doi: 10.1016/j.gde.2006.02.004. Epub 2006 Feb 28.
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Initiation of DNA repair mediated by a stalled RNA polymerase IIO.由停滞的RNA聚合酶IIO介导的DNA修复起始。
EMBO J. 2006 Jan 25;25(2):387-97. doi: 10.1038/sj.emboj.7600933. Epub 2006 Jan 12.

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