DNA糖基化酶OGG1寻找和加工8-氧鸟嘌呤的时空动态

IF 3 3区 生物学 Q2 GENETICS & HEREDITY
Luana Cintori , Anne-Marie Di Guilmi , Yvan Canitrot , Sebastien Huet , Anna Campalans
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引用次数: 0

摘要

OGG1是负责从DNA中去除氧化损伤的8-氧鸟嘌呤(8-oxoG)的DNA糖基酶。OGG1对这种病变的识别是一个复杂的过程,包括扫描DNA以寻找8-oxoG的存在,然后识别和切除病变。结构数据表明,OGG1通过不同的构象阶段进化到DNA上,对应于8-oxoG识别和从双螺旋中挤出的基本步骤。OGG1在裸DNA上的单分子研究表明,OGG1与DNA持续接触,呈现不同的结合状态,可能对应于不同的构象阶段。然而,在细胞中,DNA并不是裸露的,OGG1必须进入细胞核内复杂而高度拥挤的环境。为了确保8-oxoG的快速检测,OGG1在3D扩散和沿DNA滑动之间交替。这个过程受到局部染色质状态的调节,但也受到蛋白质辅助因子的调节,这些辅助因子可以促进氧化损伤的检测。在这里,我们将回顾过去几年来使用的不同方法,以更好地了解OGG1如何检测和处理8-oxoG病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatio-temporal dynamics of the DNA glycosylase OGG1 in finding and processing 8-oxoguanine

OGG1 is the DNA glycosylase responsible for the removal of the oxidative lesion 8-oxoguanine (8-oxoG) from DNA. The recognition of this lesion by OGG1 is a complex process that involves scanning the DNA for the presence of 8-oxoG, followed by recognition and lesion removal. Structural data have shown that OGG1 evolves through different stages of conformation onto the DNA, corresponding to elementary steps of the 8-oxoG recognition and extrusion from the double helix. Single-molecule studies of OGG1 on naked DNA have shown that OGG1 slides in persistent contact with the DNA, displaying different binding states probably corresponding to the different conformation stages. However, in cells, the DNA is not naked and OGG1 has to navigate into a complex and highly crowded environment within the nucleus. To ensure rapid detection of 8-oxoG, OGG1 alternates between 3D diffusion and sliding along the DNA. This process is regulated by the local chromatin state but also by protein co-factors that could facilitate the detection of oxidized lesions. We will review here the different methods that have been used over the last years to better understand how OGG1 detects and process 8-oxoG lesions.

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来源期刊
DNA Repair
DNA Repair 生物-毒理学
CiteScore
7.60
自引率
5.30%
发文量
91
审稿时长
59 days
期刊介绍: DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease. DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.
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