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RNAs nonspecifically inhibit RNA polymerase II by preventing binding to the DNA template

机译:RNA通过阻止与DNA模板的结合非特异性抑制RNA聚合酶II

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摘要

Many RNAs are known to act as regulators of transcription in eukaryotes, including certain small RNAs that directly inhibit RNA polymerases both in prokaryotes and eukaryotes. We have examined the potential for a variety of RNAs to directly inhibit transcription by yeast RNA polymerase II (Pol II) and find that unstructured RNAs are potent inhibitors of purified yeast Pol II. Inhibition by RNA is achieved by blocking binding of the DNA template and requires binding of the RNA to Pol II prior to open complex formation. RNA is not able to displace a DNA template that is already stably bound to Pol II, nor can RNA inhibit elongating Pol II. Unstructured RNAs are more potent inhibitors than highly structured RNAs and can also block specific transcription initiation in the presence of basal transcription factors. Crosslinking studies with ultraviolet light show that unstructured RNA is most closely associated with the two large subunits of Pol II that comprise the template binding cleft, but the RNA has contacts in a basic residue channel behind the back wall of the active site. These results are distinct from previous observations of specific inhibition by small, structured RNAs in that they demonstrate a sensitivity of the holoenzyme to inhibition by unstructured RNA products that bind to a surface outside the DNA cleft. These results are discussed in terms of the need to prevent inhibition by RNAs, either though sequestration of nascent RNA or preemptive interaction of Pol II with the DNA template.
机译:已知许多RNA充当真核生物的转录调节剂,包括某些直接抑制原核生物和真核生物中RNA聚合酶的小RNA。我们已经检查了多种RNA直接抑制酵母RNA聚合酶II(Pol II)转录的潜力,并发现非结构化RNA是纯化酵母Pol II的有效抑制剂。 RNA的抑制是通过阻断DNA模板的结合来实现的,并且需要在开放复合物形成之前将RNA与Pol II结合。 RNA不能取代已经稳定结合到Pol II的DNA模板,RNA也不能抑制延伸的Pol II。与高度结构化的RNA相比,非结构化的RNA是更有效的抑制剂,并且在存在基础转录因子的情况下,也可以阻断特定的转录起始。用紫外线进行的交联研究表明,非结构化RNA与包含模板结合裂的Pol II的两个大亚基关系最为密切,但RNA在活性位点后壁的基本残基通道中具有接触。这些结果与先前对小型结构化RNA的特异性抑制的观察结果不同,因为它们证明了全酶对结合到DNA裂口外表面的非结构化RNA产物的抑制敏感性。讨论了通过隔离新生RNA或通过Pol II与DNA模板的抢先相互作用来防止RNA抑制的需要来讨论这些结果。

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