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固定化聚合酶的转录拓扑结构。

The topology of transcription by immobilized polymerases.

作者信息

Iborra F J, Pombo A, McManus J, Jackson D A, Cook P R

机构信息

CRC Nuclear Structure and Function Research Group, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.

出版信息

Exp Cell Res. 1996 Dec 15;229(2):167-73. doi: 10.1006/excr.1996.0355.

Abstract

Current models for RNA synthesis involve an RNA polymerase that tracks along a static template. However, research on chromatin loops suggests that the template slides past a polymerase immobilized in a large transcription factory. The evidence for immobilized polymerases is reviewed, and a model for transcription by such fixed enzymes is presented. According to the model, gene activation would involve reducing gene-factory distance and increasing the affinity of a promoter for a factory. Locus controlling regions and enhancers would attach to a factory and increase the chances that a promoter could bind to a polymerase; after transcriptional termination, the gene would detach from the factory. As some RNA processing occurs cotranscriptionally, processing sites are also likely to be associated with the factory.

摘要

目前的RNA合成模型涉及一种沿着静态模板移动的RNA聚合酶。然而,对染色质环的研究表明,模板会滑过固定在大型转录工厂中的聚合酶。本文综述了固定化聚合酶的证据,并提出了由这种固定酶进行转录的模型。根据该模型,基因激活将涉及缩短基因与工厂的距离,并增加启动子对工厂的亲和力。基因座控制区和增强子将附着在工厂上,并增加启动子与聚合酶结合的机会;转录终止后,基因将从工厂上脱离。由于一些RNA加工是在转录过程中进行的,加工位点也可能与工厂相关联。

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