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本文引用的文献

1
Widespread Protection of RNA Cleavage Sites by a Riboswitch Aptamer that Folds as a Compact Obstacle to Scanning by RNase E.广泛保护 RNA 切割位点的核糖开关适体,通过折叠形成 RNase E 扫描的紧密障碍。
Mol Cell. 2021 Jan 7;81(1):127-138.e4. doi: 10.1016/j.molcel.2020.10.025. Epub 2020 Nov 18.
2
Regulation of RNA processing and degradation in bacteria.细菌中 RNA 加工和降解的调控。
Biochim Biophys Acta Gene Regul Mech. 2020 May;1863(5):194505. doi: 10.1016/j.bbagrm.2020.194505. Epub 2020 Mar 6.
3
The Vc2 Cyclic di-GMP-Dependent Riboswitch of Vibrio cholerae Regulates Expression of an Upstream Putative Small RNA by Controlling RNA Stability.霍乱弧菌的 Vc2 环二鸟苷酸依赖性核糖开关通过控制 RNA 稳定性来调节上游假定小 RNA 的表达。
J Bacteriol. 2019 Oct 4;201(21). doi: 10.1128/JB.00293-19. Print 2019 Nov 1.
4
Obstacles to Scanning by RNase E Govern Bacterial mRNA Lifetimes by Hindering Access to Distal Cleavage Sites.RNase E 阻碍对细菌 mRNA 寿命的扫描,通过阻碍对远端切割位点的接近。
Mol Cell. 2019 Apr 18;74(2):284-295.e5. doi: 10.1016/j.molcel.2019.01.044. Epub 2019 Mar 6.
5
Cyclic di-GMP Regulates TfoY in Vibrio cholerae To Control Motility by both Transcriptional and Posttranscriptional Mechanisms.环二鸟苷酸通过转录和转录后机制调节霍乱弧菌中的 TfoY 来控制运动性。
J Bacteriol. 2018 Mar 12;200(7). doi: 10.1128/JB.00578-17. Print 2018 Apr 1.
6
Riboswitch diversity and distribution.核糖开关的多样性与分布
RNA. 2017 Jul;23(7):995-1011. doi: 10.1261/rna.061234.117. Epub 2017 Apr 10.
7
Biochemical Validation of a Third Guanidine Riboswitch Class in Bacteria.细菌中第三种胍基核糖开关类别的生化验证
Biochemistry. 2017 Jan 17;56(2):359-363. doi: 10.1021/acs.biochem.6b01271. Epub 2017 Jan 6.
8
Messenger RNA degradation in bacterial cells.细菌细胞中的信使核糖核酸降解
Annu Rev Genet. 2014;48:537-59. doi: 10.1146/annurev-genet-120213-092340. Epub 2014 Oct 1.
9
A decade of riboswitches.十年的核糖开关。
Cell. 2013 Jan 17;152(1-2):17-24. doi: 10.1016/j.cell.2012.12.024.
10
Dual-acting riboswitch control of translation initiation and mRNA decay.双功能核糖开关对翻译起始和 mRNA 降解的控制。
Proc Natl Acad Sci U S A. 2012 Dec 11;109(50):E3444-53. doi: 10.1073/pnas.1214024109. Epub 2012 Nov 19.

核糖开关控制细菌 RNA 的稳定性。

Riboswitch control of bacterial RNA stability.

机构信息

Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY, USA.

Department of Microbiology, New York University School of Medicine, New York, NY, USA.

出版信息

Mol Microbiol. 2021 Aug;116(2):361-365. doi: 10.1111/mmi.14723. Epub 2021 Apr 25.

DOI:10.1111/mmi.14723
PMID:33797153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10367942/
Abstract

Although riboswitches have long been known to regulate translation initiation and transcription termination, a growing body of evidence indicates that they can also control bacterial RNA lifetimes by acting directly to hasten or impede RNA degradation. Ligand binding to the aptamer domain of a riboswitch can accelerate RNA decay by triggering a conformational change that exposes sites to endonucleolytic cleavage or by catalyzing the self-cleavage of a prefolded ribozyme. Alternatively, the conformational change induced by ligand binding can protect RNA from degradation by blocking access to an RNA terminus or internal region that would otherwise be susceptible to attack by an exonuclease or endonuclease. Such changes in RNA longevity often accompany a parallel effect of the same riboswitch on translation or transcription. Consequently, a single riboswitch aptamer may govern the function of multiple effector elements (expression platforms) that are co-resident within a transcript and act independently of one another.

摘要

尽管核糖开关早已被证实可以调节翻译起始和转录终止,但越来越多的证据表明,它们还可以通过直接作用来加速或阻碍 RNA 降解,从而控制细菌 RNA 的寿命。配体与核糖开关的适体结构域结合,可以通过触发构象变化来加速 RNA 降解,这种构象变化会暴露出易被内切核酸酶切割的位点,或者通过催化预折叠核酶的自我切割来实现。或者,配体结合所诱导的构象变化可以通过阻止 RNA 末端或内部区域被外切核酸酶或内切核酸酶攻击,从而保护 RNA 免受降解。这种 RNA 寿命的变化通常伴随着同一核糖开关对翻译或转录的平行影响。因此,单个核糖开关适体可能控制多个效应元件(表达平台)的功能,这些效应元件共同存在于一个转录本中,并相互独立地发挥作用。