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转录复合物作为 RNA 分子伴侣。

Transcription complexes as RNA chaperones.

机构信息

Freie Universität Berlin, Department Biology, Chemistry, Pharmacy, Institute of Chemistry and Biochemistry, Laboratory of Structural Biochemistry, Berlin, Germany.

Helmholtz-Zentrum Berlin Für Materialien Und Energie, Macromolecular Crystallography, Berlin, Germany.

出版信息

Transcription. 2021 Aug;12(4):126-155. doi: 10.1080/21541264.2021.1985931. Epub 2021 Nov 1.

DOI:10.1080/21541264.2021.1985931
PMID:34719334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8632103/
Abstract

To exert their functions, RNAs adopt diverse structures, ranging from simple secondary to complex tertiary and quaternary folds. , RNA folding starts with RNA transcription, and a wide variety of processes are coupled to co-transcriptional RNA folding events, including the regulation of fundamental transcription dynamics, gene regulation by mechanisms like attenuation, RNA processing or ribonucleoprotein particle formation. While co-transcriptional RNA folding and associated co-transcriptional processes are by now well accepted as pervasive regulatory principles in all organisms, investigations into the role of the transcription machinery in co-transcriptional folding processes have so far largely focused on effects of the order in which RNA regions are produced and of transcription kinetics. Recent structural and structure-guided functional analyses of bacterial transcription complexes increasingly point to an additional role of RNA polymerase and associated transcription factors in supporting co-transcriptional RNA folding by fostering or preventing strategic contacts to the nascent transcripts. In general, the results support the view that transcription complexes can act as RNA chaperones, a function that has been suggested over 30 years ago. Here, we discuss transcription complexes as RNA chaperones based on recent examples from bacterial transcription.

摘要

为了发挥其功能,RNA 采用了多种结构,从简单的二级结构到复杂的三级和四级折叠。RNA 折叠始于 RNA 转录,许多过程与共转录 RNA 折叠事件相关联,包括基本转录动力学的调节、衰减等机制的基因调节、RNA 加工或核糖核蛋白颗粒形成。虽然共转录 RNA 折叠和相关的共转录过程现在被普遍认为是所有生物中普遍存在的调节原则,但对转录机制在共转录折叠过程中的作用的研究迄今为止主要集中在 RNA 区域产生的顺序和转录动力学的影响上。最近对细菌转录复合物的结构和结构导向功能分析越来越多地表明,RNA 聚合酶和相关转录因子通过促进或阻止与新生转录本的战略接触,在支持共转录 RNA 折叠方面发挥额外作用。一般来说,这些结果支持了转录复合物可以作为 RNA 分子伴侣的观点,这一观点早在 30 多年前就被提出。在这里,我们基于细菌转录的最新例子,讨论转录复合物作为 RNA 分子伴侣的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b8fbe4869375/KTRN_A_1985931_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/02cb0a6a3840/KTRN_A_1985931_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b17fd60d1cbb/KTRN_A_1985931_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/977f10256297/KTRN_A_1985931_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/e43a2377c9cc/KTRN_A_1985931_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b6c789d725df/KTRN_A_1985931_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/dc9448fb37d6/KTRN_A_1985931_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b8fbe4869375/KTRN_A_1985931_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/02cb0a6a3840/KTRN_A_1985931_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b17fd60d1cbb/KTRN_A_1985931_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/977f10256297/KTRN_A_1985931_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/e43a2377c9cc/KTRN_A_1985931_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b6c789d725df/KTRN_A_1985931_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/dc9448fb37d6/KTRN_A_1985931_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536f/8632103/b8fbe4869375/KTRN_A_1985931_F0007_OC.jpg

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本文引用的文献

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