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Bending the Rules of Transcriptional Repression: Tightly Looped DNA Directly Represses T7 RNA Polymerase

机译:弯曲转录抑制规则:紧环的DNA直接抑制T7 RNA聚合酶

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摘要

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 ∼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.
机译:从超螺旋DNA到某些基因阻遏物形成的DNA紧密环,细胞中的DNA通常高度弯曲。尽管有证据表明在DNA严重变形的系统中RNA聚合酶(RNAP)的转录会受到影响,但是聚合酶功能与机械应力DNA之间关系的机制细节仍不清楚。为了进一步了解高度弯曲的DNA的调控结果,我们推测紧密环合的DNA足以抑制转录。为了检验该假设,我们开发了一种测定方法,以定量检测噬菌体T7 RNAP在大小约为100 bp的小型圆形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合成能力可以被抑制至少两个数量级。此外,我们显示维持可变水平的扭曲的小圆模板仅产生适度的压制效率差异。因此,我们得出的结论是,微圆模板内的弯曲力学控制着观察到的压制。我们的结果支持一个模型,其中RNAP功能高度依赖于DNA的弯曲机制,并暗示了模板本身在已知DNA高度弯曲的调节系统中所发挥的直接调节作用。

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