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直接检测转录中夭折循环的能量基础。

Direct tests of the energetic basis of abortive cycling in transcription.

机构信息

Program in Molecular & Cellular Biology, University of Massachusetts, Amherst, Massachusetts 01003, United States.

出版信息

Biochemistry. 2011 Aug 16;50(32):7015-22. doi: 10.1021/bi200620q. Epub 2011 Jul 21.

Abstract

Although the synthesis of RNA from a DNA template is (and must be) a generally very stable process to enable transcription of kilobase transcripts, it has long been known that during initial transcription of the first 8-10 bases of RNA complexes are relatively unstable, leading to the release of short abortive RNA transcripts. A wealth of structural data in the past decade has led to specific mechanistic models elaborating an earlier "stressed intermediate" model for initial transcription. In this study, we test fundamental predictions of each of these models in the simple model enzyme T7 RNA polymerase. Nicking or gapping the nontranscribed template DNA immediately upstream of the growing hybrid yields no systematic reduction in abortive falloff, demonstrating clearly that compaction or "scrunching" of this DNA is not a source of functional instability. Similarly, transcription on DNA in which the nontemplate strand in the initially transcribed region is either mismatched or removed altogether leads to at most modest reductions in abortive falloff, indicating that expansion or "scrunching" of the bubble is not the primary driving force for abortive cycling. Finally, energetic stress derived from the observed steric clash of the growing hybrid against the N-terminal domain contributes at most mildly to abortive cycling, as the addition of steric bulk (additional RNA bases) at the upstream end of the hybrid does not lead to predicted positional shifts in observed abortive patterns. We conclude that while structural changes (scrunching) clearly occur in initial transcription, stress from these changes is not the primary force driving abortive cycling.

摘要

尽管从 DNA 模板合成 RNA (并且必须是)是一个非常稳定的过程,以实现千碱基转录物的转录,但长期以来,人们一直知道,在 RNA 复合物最初转录的前 8-10 个碱基时,复合物相对不稳定,导致短的无意义 RNA 转录物的释放。过去十年中的大量结构数据导致了特定的机制模型,详细阐述了初始转录的早期“应激中间体”模型。在这项研究中,我们在简单的 T7 RNA 聚合酶模型酶中测试了这些模型中的每一个的基本预测。在生长杂交物的上游非转录模板 DNA 上进行缺口或缺口处理不会导致无意义脱落的系统减少,这清楚地表明该 DNA 的紧凑或“压缩”不是功能不稳定的来源。同样,在最初转录区域的非模板链要么错配要么完全去除的 DNA 上进行转录,导致无意义脱落的减少最多适度,表明泡的膨胀或“压缩”不是无意义循环的主要驱动力。最后,观察到的生长杂交物与 N 端结构域之间的空间冲突所产生的能量压力最多只会轻度导致无意义循环,因为在杂交物的上游端添加空间位阻(更多的 RNA 碱基)不会导致观察到的无意义模式中的预测位置变化。我们得出结论,尽管在初始转录中确实会发生结构变化(压缩),但这些变化的压力不是驱动无意义循环的主要力量。

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