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在辐射诱导的 DNA 损伤下 DNA-蛋白质复合物形成的原位分析。

In Situ Analysis of DNA-Protein Complex Formation upon Radiation-Induced DNA Damage.

机构信息

Istituto di Genetica Molecolare "Luca Cavalli Sforza", Consiglio Nazionale delle Ricerche (CNR), 27100 Pavia, Italy.

Dipartimento di Biologia e Biotecnologie, Università di Pavia, 27100 Pavia, Italy.

出版信息

Int J Mol Sci. 2019 Nov 15;20(22):5736. doi: 10.3390/ijms20225736.

DOI:10.3390/ijms20225736
PMID:31731696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6888283/
Abstract

The importance of determining at the cellular level the formation of DNA-protein complexes after radiation-induced lesions to DNA is outlined by the evidence that such interactions represent one of the first steps of the cellular response to DNA damage. These complexes are formed through recruitment at the sites of the lesion, of proteins deputed to signal the presence of DNA damage, and of DNA repair factors necessary to remove it. Investigating the formation of such complexes has provided, and will probably continue to, relevant information about molecular mechanisms and spatiotemporal dynamics of the processes that constitute the first barrier of cell defense against genome instability and related diseases. In this review, we will summarize and discuss the use of in situ procedures to detect the formation of DNA-protein complexes after radiation-induced DNA damage. This type of analysis provides important information on the spatial localization and temporal resolution of the formation of such complexes, at the single-cell level, allowing the study of heterogeneous cell populations.

摘要

在细胞水平上确定 DNA 损伤后 DNA-蛋白质复合物的形成对于阐明辐射诱导损伤后细胞对 DNA 损伤的反应的第一步之一,即这种相互作用具有重要意义。这些复合物是通过募集到损伤部位的、负责信号传递的蛋白质以及修复损伤所必需的 DNA 修复因子而形成的。研究这些复合物的形成提供了,并可能继续提供有关构成细胞抵御基因组不稳定性和相关疾病第一道防线的分子机制和时空动力学的相关信息。在这篇综述中,我们将总结和讨论使用原位程序来检测辐射诱导的 DNA 损伤后 DNA-蛋白质复合物的形成。这种分析类型提供了关于此类复合物形成的空间定位和时间分辨率的重要信息,在单细胞水平上,可以研究异质细胞群体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/6888283/d842683facc0/ijms-20-05736-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/6888283/55bd02fadca3/ijms-20-05736-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/6888283/d842683facc0/ijms-20-05736-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/6888283/55bd02fadca3/ijms-20-05736-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1e/6888283/d842683facc0/ijms-20-05736-g002.jpg

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Nucleic Acids Res. 2019 Dec 2;47(21):11250-11267. doi: 10.1093/nar/gkz820.
2
Systematic analysis of DNA damage induction and DNA repair pathway activation by continuous wave visible light laser micro-irradiation.连续波可见光激光微照射诱导DNA损伤及激活DNA修复途径的系统分析
AIMS Genet. 2017 Feb 21;4(1):47-68. doi: 10.3934/genet.2017.1.47. eCollection 2017.
3
Inhibition of Karyopherin-α2 Augments Radiation-Induced Cell Death by Perturbing BRCA1-Mediated DNA Repair.
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Int J Mol Sci. 2019 Jun 11;20(11):2843. doi: 10.3390/ijms20112843.
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Fluorescently-labelled CPD and 6-4PP photolyases: new tools for live-cell DNA damage quantification and laser-assisted repair.荧光标记的 CPD 和 6-4PP 光解酶:用于活细胞 DNA 损伤定量和激光辅助修复的新工具。
Nucleic Acids Res. 2019 Apr 23;47(7):3536-3549. doi: 10.1093/nar/gkz035.
5
Targeting DNA Double-Strand Break Repair Pathways to Improve Radiotherapy Response.靶向 DNA 双链断裂修复途径以提高放射治疗反应。
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6
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Methods. 2019 Mar 15;157:80-87. doi: 10.1016/j.ymeth.2018.11.004. Epub 2018 Nov 10.
7
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9
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10
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