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本文引用的文献

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The task force that rescues stalled ribosomes in bacteria.负责救援细菌中停滞核糖体的工作组。
Trends Biochem Sci. 2013 Aug;38(8):403-11. doi: 10.1016/j.tibs.2013.06.002. Epub 2013 Jun 30.
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Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP function.真核细胞应激颗粒通过自噬和 Cdc48/VCP 功能被清除。
Cell. 2013 Jun 20;153(7):1461-74. doi: 10.1016/j.cell.2013.05.037.
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An RNA degradation machine sculpted by Ro autoantigen and noncoding RNA.Ro 自身抗原和非编码 RNA 塑造的 RNA 降解机器。
Cell. 2013 Mar 28;153(1):166-77. doi: 10.1016/j.cell.2013.02.037.
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Mycobacterium tuberculosis MutT1 (Rv2985) and ADPRase (Rv1700) proteins constitute a two-stage mechanism of 8-oxo-dGTP and 8-oxo-GTP detoxification and adenosine to cytidine mutation avoidance.结核分枝杆菌 MutT1(Rv2985)和 ADPRase(Rv1700)蛋白构成了 8-氧代-dGTP 和 8-氧代-GTP 解毒以及腺嘌呤向胞嘧啶突变避免的两阶段机制。
J Biol Chem. 2013 Apr 19;288(16):11252-62. doi: 10.1074/jbc.M112.442566. Epub 2013 Mar 5.
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Elimination and utilization of oxidized guanine nucleotides in the synthesis of RNA and its precursors.在 RNA 及其前体的合成中氧化鸟嘌呤核苷酸的消除和利用。
J Biol Chem. 2013 Mar 22;288(12):8128-8135. doi: 10.1074/jbc.M112.418723. Epub 2013 Feb 3.
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Human and methodological sources of variability in the measurement of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine.尿 8-氧-7,8-二氢-2'-脱氧鸟苷测量中的人和方法学变异源。
Antioxid Redox Signal. 2013 Jun 20;18(18):2377-91. doi: 10.1089/ars.2012.4714. Epub 2013 Jan 31.
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Association between urinary markers of nucleic acid oxidation and mortality in type 2 diabetes: a population-based cohort study.尿液核酸氧化标志物与 2 型糖尿病患者死亡率的相关性:一项基于人群的队列研究。
Diabetes Care. 2013 Mar;36(3):669-76. doi: 10.2337/dc12-0998. Epub 2012 Nov 12.
8
The Yersinia pseudotuberculosis degradosome is required for oxidative stress, while its PNPase subunit plays a degradosome-independent role in cold growth.耶尔森氏菌假结核降解体对于氧化应激是必需的,而其 PNPase 亚基在冷生长中发挥降解体非依赖性作用。
FEMS Microbiol Lett. 2012 Nov;336(2):139-47. doi: 10.1111/j.1574-6968.12000.x. Epub 2012 Sep 24.
9
Nucleolar accumulation of APE1 depends on charged lysine residues that undergo acetylation upon genotoxic stress and modulate its BER activity in cells.核仁中 APE1 的积累依赖于带电赖氨酸残基,这些残基在遗传毒性应激下发生乙酰化修饰,并调节其在细胞中的 BER 活性。
Mol Biol Cell. 2012 Oct;23(20):4079-96. doi: 10.1091/mbc.E12-04-0299. Epub 2012 Aug 23.
10
Characterization of RNA damage under oxidative stress in Escherichia coli.在大肠杆菌氧化应激下的 RNA 损伤特征。
Biol Chem. 2012 Mar;393(3):123-32. doi: 10.1515/hsz-2011-0247.

对抗 RNA 氧化:降低氧化 RNA 以保护细胞的分子机制。

Battle against RNA oxidation: molecular mechanisms for reducing oxidized RNA to protect cells.

机构信息

Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL, USA.

出版信息

Wiley Interdiscip Rev RNA. 2014 May-Jun;5(3):335-46. doi: 10.1002/wrna.1214. Epub 2013 Dec 16.

DOI:10.1002/wrna.1214
PMID:24375979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3991771/
Abstract

Oxidation is probably the most common type of damage that occurs in cellular RNA. Oxidized RNA may be dysfunctional and is implicated in the pathogenesis of age-related human diseases. Cellular mechanisms controlling oxidized RNA have begun to be revealed. Currently, a number of ribonucleases and RNA-binding proteins have been shown to reduce oxidized RNA and to protect cells under oxidative stress. Although information about how these factors work is still very limited, we suggest several mechanisms that can be used to minimize oxidized RNA in various organisms.

摘要

氧化可能是细胞 RNA 中最常见的损伤类型。氧化的 RNA 可能失去功能,并与与年龄相关的人类疾病的发病机制有关。控制氧化 RNA 的细胞机制已开始被揭示。目前,已经证明许多核糖核酸酶和 RNA 结合蛋白可以减少氧化 RNA,并在氧化应激下保护细胞。尽管关于这些因素如何发挥作用的信息仍然非常有限,但我们提出了几种可以用于最大限度减少各种生物体中氧化 RNA 的机制。