• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

8-氧代-7,8-二氢鸟嘌呤:与基因表达、衰老和抵御氧化应激的联系。

8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress.

机构信息

Research Institute of Sport Science, Faculty of Physical Education and Sport Science, Semmelweis University, Budapest, Hungary.

出版信息

Free Radic Biol Med. 2010 Aug 15;49(4):587-96. doi: 10.1016/j.freeradbiomed.2010.05.008. Epub 2010 May 17.

DOI:10.1016/j.freeradbiomed.2010.05.008
PMID:20483371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2943936/
Abstract

The one-electron oxidation product of guanine, 8-oxo-7,8-dihydroguanine (8-oxoG), is an abundant lesion in genomic, mitochondrial, and telomeric DNA and RNA. It is considered to be a marker of oxidative stress that preferentially accumulates at the 5' end of guanine strings in the DNA helix, in guanine quadruplexes, and in RNA molecules. 8-OxoG has a lower oxidation potential compared to guanine; thus it is susceptible to oxidation/reduction and, along with its redox products, is traditionally considered to be a major mutagenic DNA base lesion. It does not change the architecture of the DNA double helix and it is specifically recognized and excised by 8-oxoguanine DNA glycosylase (OGG1) during the DNA base excision repair pathway. OGG1 null animals accumulate excess levels of 8-oxoG in their genome, yet they do not have shorter life span nor do they exhibit severe pathological symptoms including tumor formation. In fact they are increasingly resistant to inflammation. Here we address the rarely considered significance of 8-oxoG, such as its optimal levels in DNA and RNA under a given condition, essentiality for normal cellular physiology, evolutionary role, and ability to soften the effects of oxidative stress in DNA, and the harmful consequences of its repair, as well as its importance in transcriptional initiation and chromatin relaxation.

摘要

鸟嘌呤的单电子氧化产物 8-氧代-7,8-二氢鸟嘌呤(8-oxoG)是基因组、线粒体和端粒 DNA 和 RNA 中的大量损伤。它被认为是氧化应激的标志物,优先积累在 DNA 螺旋中鸟嘌呤串的 5'端、鸟嘌呤四联体和 RNA 分子中。与鸟嘌呤相比,8-oxoG 的氧化还原电位较低;因此,它易发生氧化/还原,并且与它的氧化还原产物一起,传统上被认为是主要的致突变 DNA 碱基损伤。它不会改变 DNA 双螺旋的结构,并且在 DNA 碱基切除修复途径中,它被 8-氧鸟嘌呤 DNA 糖基化酶(OGG1)特异性识别和切除。OGG1 缺失的动物在其基因组中积累过多的 8-oxoG,但它们的寿命没有缩短,也没有表现出严重的病理症状,包括肿瘤形成。事实上,它们对炎症的抵抗力越来越强。在这里,我们探讨了 8-oxoG 的很少被考虑的意义,例如在给定条件下其在 DNA 和 RNA 中的最佳水平、对正常细胞生理学的必要性、进化作用以及在 DNA 中减轻氧化应激影响的能力,以及其修复的有害后果,以及它在转录起始和染色质松弛中的重要性。

相似文献

1
8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress.8-氧代-7,8-二氢鸟嘌呤:与基因表达、衰老和抵御氧化应激的联系。
Free Radic Biol Med. 2010 Aug 15;49(4):587-96. doi: 10.1016/j.freeradbiomed.2010.05.008. Epub 2010 May 17.
2
Repair of 8-oxo-7,8-dihydroguanine in prokaryotic and eukaryotic cells: Properties and biological roles of the Fpg and OGG1 DNA N-glycosylases.原核细胞和真核细胞中8-氧代-7,8-二氢鸟嘌呤的修复:Fpg和OGG1 DNA N-糖基化酶的特性及生物学作用
Free Radic Biol Med. 2017 Jun;107:179-201. doi: 10.1016/j.freeradbiomed.2016.11.042. Epub 2016 Nov 27.
3
8-Oxoguanine DNA glycosylase 1: Beyond repair of the oxidatively modified base lesions.8-氧鸟嘌呤 DNA 糖基化酶 1:超越氧化碱基损伤的修复。
Redox Biol. 2018 Apr;14:669-678. doi: 10.1016/j.redox.2017.11.008. Epub 2017 Nov 10.
4
Lost in the Crowd: How Does Human 8-Oxoguanine DNA Glycosylase 1 (OGG1) Find 8-Oxoguanine in the Genome?湮没于众:人 8-氧鸟嘌呤 DNA 糖基化酶 1(OGG1)如何在基因组中找到 8-氧鸟嘌呤?
Int J Mol Sci. 2020 Nov 7;21(21):8360. doi: 10.3390/ijms21218360.
5
The role of 8-oxoguanine DNA glycosylase-1 in inflammation.8-氧代鸟嘌呤DNA糖基化酶-1在炎症中的作用。
Int J Mol Sci. 2014 Sep 23;15(9):16975-97. doi: 10.3390/ijms150916975.
6
8-Oxoguanine DNA glycosylase-1 links DNA repair to cellular signaling via the activation of the small GTPase Rac1.8-氧代鸟嘌呤DNA糖基化酶-1通过激活小GTP酶Rac1将DNA修复与细胞信号传导联系起来。
Free Radic Biol Med. 2013 Aug;61:384-94. doi: 10.1016/j.freeradbiomed.2013.04.011. Epub 2013 Apr 21.
7
Activation of cellular signaling by 8-oxoguanine DNA glycosylase-1-initiated DNA base excision repair.8-氧鸟嘌呤 DNA 糖基化酶 1 起始的 DNA 碱基切除修复激活细胞信号转导。
DNA Repair (Amst). 2013 Oct;12(10):856-63. doi: 10.1016/j.dnarep.2013.06.006. Epub 2013 Jul 25.
8
Biochemical identification of a hydroperoxide derivative of the free 8-oxo-7,8-dihydroguanine base.游离 8-氧代-7,8-二氢鸟嘌呤碱基的过氧化物衍生物的生化鉴定。
Free Radic Biol Med. 2012 Feb 15;52(4):749-56. doi: 10.1016/j.freeradbiomed.2011.11.015. Epub 2011 Dec 1.
9
Whole transcriptome analysis reveals an 8-oxoguanine DNA glycosylase-1-driven DNA repair-dependent gene expression linked to essential biological processes.全转录组分析揭示了一种由8-氧代鸟嘌呤DNA糖基化酶-1驱动的、与基本生物学过程相关的DNA修复依赖性基因表达。
Free Radic Biol Med. 2015 Apr;81:107-18. doi: 10.1016/j.freeradbiomed.2015.01.004. Epub 2015 Jan 19.
10
8-Oxoguanine DNA glycosylase-1-mediated DNA repair is associated with Rho GTPase activation and α-smooth muscle actin polymerization.8-氧代鸟嘌呤DNA糖基化酶-1介导的DNA修复与Rho GTP酶激活及α-平滑肌肌动蛋白聚合有关。
Free Radic Biol Med. 2014 Aug;73:430-8. doi: 10.1016/j.freeradbiomed.2014.03.030. Epub 2014 Mar 26.

引用本文的文献

1
Hormesis and Muscle Plasticity.兴奋效应与肌肉可塑性
Adv Exp Med Biol. 2025;1478:85-100. doi: 10.1007/978-3-031-88361-3_5.
2
Photoaging: UV radiation-induced cGAS-STING signaling promotes the aging process in skin by remodeling the immune network.光老化:紫外线辐射诱导的cGAS-STING信号通路通过重塑免疫网络促进皮肤衰老进程。
Biogerontology. 2025 Jun 20;26(4):123. doi: 10.1007/s10522-025-10268-1.
3
Chemical Switching: A Concept Inspired by Strategies from Biocatalysis and Organocatalysis.化学开关:受生物催化和有机催化策略启发的概念

本文引用的文献

1
Reactive oxygen species: A radical role in development?活性氧物种:在发育中起关键作用?
Free Radic Biol Med. 2010 Jul 15;49(2):130-43. doi: 10.1016/j.freeradbiomed.2010.03.020. Epub 2010 Mar 29.
2
How increased oxidative stress promotes longevity and metabolic health: The concept of mitochondrial hormesis (mitohormesis).氧化应激如何促进长寿和代谢健康:线粒体应激(mitohormesis)的概念。
Exp Gerontol. 2010 Jun;45(6):410-8. doi: 10.1016/j.exger.2010.03.014. Epub 2010 Mar 27.
3
Oxidative damage to RNA: mechanisms, consequences, and diseases.
Chembiochem. 2025 Jun 3;26(11):e202500220. doi: 10.1002/cbic.202500220. Epub 2025 May 26.
4
OGG1S326C variant frequent in human populations facilitates inflammatory responses due to its extended interaction with DNA substrate.人类群体中常见的OGG1 S326C变体因其与DNA底物的广泛相互作用而促进炎症反应。
Proc Natl Acad Sci U S A. 2025 May 13;122(19):e2426102122. doi: 10.1073/pnas.2426102122. Epub 2025 May 9.
5
Immune response accelerated telomere shortening during early life stage of a passerine bird, the blue tit ().免疫反应加速了鸣禽蓝山雀早期生命阶段的端粒缩短。
Biol Lett. 2025 Jan;21(1):20240618. doi: 10.1098/rsbl.2024.0618. Epub 2025 Jan 22.
6
Reassessing the roles of oxidative DNA base lesion 8-oxoGua and repair enzyme OGG1 in tumorigenesis.重新评估氧化性DNA碱基损伤8-氧代鸟嘌呤(8-oxoGua)和修复酶OGG1在肿瘤发生中的作用。
J Biomed Sci. 2025 Jan 1;32(1):1. doi: 10.1186/s12929-024-01093-8.
7
Recent Advance in Single-Molecule Fluorescent Biosensors for Tumor Biomarker Detection.近年来用于肿瘤生物标志物检测的单分子荧光生物传感器的研究进展。
Biosensors (Basel). 2024 Nov 7;14(11):540. doi: 10.3390/bios14110540.
8
Selective 8-oxo-rG stalling occurs in the catalytic core of polynucleotide phosphorylase (PNPase) during degradation.在多核苷酸磷酸化酶(PNPase)的催化核心中,8-氧代-rG 选择性停滞发生在降解过程中。
Proc Natl Acad Sci U S A. 2024 Nov 12;121(46):e2317865121. doi: 10.1073/pnas.2317865121. Epub 2024 Nov 4.
9
Skin senescence-from basic research to clinical practice.皮肤衰老——从基础研究到临床实践
Front Med (Lausanne). 2024 Oct 18;11:1484345. doi: 10.3389/fmed.2024.1484345. eCollection 2024.
10
Oxidative stress: fundamentals and advances in quantification techniques.氧化应激:量化技术的基础与进展
Front Chem. 2024 Oct 7;12:1470458. doi: 10.3389/fchem.2024.1470458. eCollection 2024.
RNA 的氧化损伤:机制、后果与疾病。
Cell Mol Life Sci. 2010 Jun;67(11):1817-29. doi: 10.1007/s00018-010-0277-y. Epub 2010 Feb 11.
4
Reactive oxygen species, cellular redox systems, and apoptosis.活性氧、细胞氧化还原系统与细胞凋亡。
Free Radic Biol Med. 2010 Mar 15;48(6):749-62. doi: 10.1016/j.freeradbiomed.2009.12.022. Epub 2010 Jan 4.
5
Redox homeostasis and cellular stress response in aging and neurodegeneration.衰老与神经退行性变中的氧化还原稳态和细胞应激反应
Methods Mol Biol. 2010;610:285-308. doi: 10.1007/978-1-60327-029-8_17.
6
Encounter and extrusion of an intrahelical lesion by a DNA repair enzyme.DNA 修复酶对内切酶损伤的遇合与挤出
Nature. 2009 Dec 10;462(7274):762-6. doi: 10.1038/nature08561.
7
Exercise alters SIRT1, SIRT6, NAD and NAMPT levels in skeletal muscle of aged rats.运动改变老年大鼠骨骼肌中的 SIRT1、SIRT6、NAD 和 NAMPT 水平。
Mech Ageing Dev. 2010 Jan;131(1):21-8. doi: 10.1016/j.mad.2009.11.002. Epub 2009 Nov 12.
8
Reactive oxygen species are signalling molecules for skeletal muscle adaptation.活性氧是骨骼肌适应的信号分子。
Exp Physiol. 2010 Jan;95(1):1-9. doi: 10.1113/expphysiol.2009.050526. Epub 2009 Oct 30.
9
The DNA-damage response in human biology and disease.人类生物学与疾病中的DNA损伤反应
Nature. 2009 Oct 22;461(7267):1071-8. doi: 10.1038/nature08467.
10
Tumour suppression by p53: a role for the DNA damage response?p53介导的肿瘤抑制作用:DNA损伤反应起作用吗?
Nat Rev Cancer. 2009 Oct;9(10):714-23. doi: 10.1038/nrc2716. Epub 2009 Sep 4.