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Elucidation of the Clustered Nano-Architecture of Radiation-Induced DNA Damage Sites and Surrounding Chromatin in Cancer Cells: A Single Molecule Localization Microscopy Approach
M. Hausmann, M. Falk, C. Neitzel, A. Hofmann, A. Biswas, T. Gier, I. Falkova, DW. Heermann, G. Hildenbrand
Language English Country Switzerland
Document type Journal Article
Grant support
the Heidelberg University Mobility Grant for International Research Cooperation within the excellence initiative II of the Deutsche Forschungsgemeinschaft (DFG)
Deutsche Forschungsgemeinschaft
H1601/16-1
Deutsche Forschungsgemeinschaft
DAAD-19-03
DAAD-CAS
GACR 20-04109J
Grantová Agentura České Republiky
The projects of Czech Government Plenipotentiary
Czech Ministry of Education, Youth and Sports (MEYS-CR)
The Project 3 + 3 for cooperation with JINR Dubna
Czech Ministry of Education, Youth and Sports (MEYS-CR)
NLK
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PubMed
33807337
DOI
10.3390/ijms22073636
Knihovny.cz E-resources
- MeSH
- Chromatin genetics ultrastructure MeSH
- DNA Breaks, Double-Stranded radiation effects MeSH
- HeLa Cells MeSH
- Radiation, Ionizing MeSH
- Humans MeSH
- Microscopy methods MeSH
- Cell Line, Tumor MeSH
- Neoplasms genetics MeSH
- DNA Repair genetics radiation effects MeSH
- DNA Damage genetics radiation effects MeSH
- Single Molecule Imaging methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
In cancer therapy, the application of (fractionated) harsh radiation treatment is state of the art for many types of tumors. However, ionizing radiation is a "double-edged sword"-it can kill the tumor but can also promote the selection of radioresistant tumor cell clones or even initiate carcinogenesis in the normal irradiated tissue. Individualized radiotherapy would reduce these risks and boost the treatment, but its development requires a deep understanding of DNA damage and repair processes and the corresponding control mechanisms. DNA double strand breaks (DSBs) and their repair play a critical role in the cellular response to radiation. In previous years, it has become apparent that, beyond genetic and epigenetic determinants, the structural aspects of damaged chromatin (i.e., not only of DSBs themselves but also of the whole damage-surrounding chromatin domains) form another layer of complex DSB regulation. In the present article, we summarize the application of super-resolution single molecule localization microscopy (SMLM) for investigations of these structural aspects with emphasis on the relationship between the nano-architecture of radiation-induced repair foci (IRIFs), represented here by γH2AX foci, and their chromatin environment. Using irradiated HeLa cell cultures as an example, we show repair-dependent rearrangements of damaged chromatin and analyze the architecture of γH2AX repair clusters according to topological similarities. Although HeLa cells are known to have highly aberrant genomes, the topological similarity of γH2AX was high, indicating a functional, presumptively genome type-independent relevance of structural aspects in DSB repair. Remarkably, nano-scaled chromatin rearrangements during repair depended both on the chromatin domain type and the treatment. Based on these results, we demonstrate how the nano-architecture and topology of IRIFs and chromatin can be determined, point to the methodological relevance of SMLM, and discuss the consequences of the observed phenomena for the DSB repair network regulation or, for instance, radiation treatment outcomes.
Institute for Theoretical Physics Heidelberg University 69120 Heidelberg Germany
Institute of Biophysics Czech Academy of Sciences 612 65 Brno Czech Republic
Kirchhoff Institute for Physics Heidelberg University 69120 Heidelberg Germany
References provided by Crossref.org
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