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打破转录抑制的规则:紧密环化的 DNA 直接抑制 T7 RNA 聚合酶。

Bending the rules of transcriptional repression: tightly looped DNA directly represses T7 RNA polymerase.

机构信息

Cellular and Molecular Biology Program, Department of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Biophys J. 2010 Aug 9;99(4):1139-48. doi: 10.1016/j.bpj.2010.04.074.

Abstract

From supercoiled DNA to the tight loops of DNA formed by some gene repressors, DNA in cells is often highly bent. Despite evidence that transcription by RNA polymerase (RNAP) is affected in systems where DNA is deformed significantly, the mechanistic details underlying the relationship between polymerase function and mechanically stressed DNA remain unclear. Seeking to gain additional insight into the regulatory consequences of highly bent DNA, we hypothesize that tightly looping DNA is alone sufficient to repress transcription. To test this hypothesis, we have developed an assay to quantify transcription elongation by bacteriophage T7 RNAP on small, circular DNA templates approximately 100 bp in size. From these highly bent transcription templates, we observe that the elongation velocity and processivity can be repressed by at least two orders of magnitude. Further, we show that minicircle templates sustaining variable levels of twist yield only moderate differences in repression efficiency. We therefore conclude that the bending mechanics within the minicircle templates dominate the observed repression. Our results support a model in which RNAP function is highly dependent on the bending mechanics of DNA and are suggestive of a direct, regulatory role played by the template itself in regulatory systems where DNA is known to be highly bent.

摘要

从超螺旋 DNA 到某些基因抑制剂形成的紧密 DNA 环,细胞内的 DNA 通常高度弯曲。尽管有证据表明,在 DNA 明显变形的系统中,RNA 聚合酶 (RNAP) 的转录受到影响,但聚合酶功能与机械应力 DNA 之间关系的机制细节仍不清楚。为了深入了解高度弯曲 DNA 的调控后果,我们假设紧密的 DNA 环本身足以抑制转录。为了验证这一假设,我们开发了一种测定方法,用于定量噬菌体 T7 RNAP 在大约 100bp 大小的小圆形 DNA 模板上的转录延伸。从这些高度弯曲的转录模板中,我们观察到延伸速度和连续性至少可以被抑制两个数量级。此外,我们表明,维持不同扭转程度的微环模板仅在抑制效率上产生适度差异。因此,我们得出结论,微环模板内的弯曲力学主导了观察到的抑制作用。我们的结果支持这样一种模型,即 RNAP 的功能高度依赖于 DNA 的弯曲力学,并且暗示在已知 DNA 高度弯曲的调控系统中,模板本身在调控中发挥直接的作用。

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本文引用的文献

1
Kinking the double helix by bending deformation.
Nucleic Acids Res. 2008 Mar;36(4):1120-8. doi: 10.1093/nar/gkm1125. Epub 2007 Dec 20.
2
Observed instability of T7 RNA polymerase elongation complexes can be dominated by collision-induced "bumping".
J Biol Chem. 2006 Aug 25;281(34):24441-8. doi: 10.1074/jbc.M604369200. Epub 2006 Jun 30.
3
DNA looping: the consequences and its control.
Curr Opin Struct Biol. 2006 Jun;16(3):344-50. doi: 10.1016/j.sbi.2006.05.008. Epub 2006 May 22.
4
Promoter unwinding and promoter clearance by RNA polymerase: detection by single-molecule DNA nanomanipulation.
Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):4776-80. doi: 10.1073/pnas.0307241101. Epub 2004 Mar 22.
6
Mechanisms of transcriptional repression.
Curr Opin Microbiol. 2001 Apr;4(2):145-51. doi: 10.1016/s1369-5274(00)00180-6.
10
The function of auxiliary operators.
Mol Microbiol. 1998 Jul;29(1):13-8. doi: 10.1046/j.1365-2958.1998.00870.x.

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