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bioRxiv · 10.1101/638361

Quantification of DNA damage induced γH2AX focus formation via super-resolution dSTORM localization microscopy

Varga, D.·Majoros, H.·Ujfaludi, Z.·Erdelyi, M.·Pankotai, T.
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Abstract

In eukaryotic cells, each process, in which DNA is involved, should take place in the context of chromatin structure. DNA double-strand breaks (DSBs) are one of the most deleterious damages often leading to chromosomal rearrangement. In response to environmental stresses, cells have developed repair mechanisms to eliminate the DSBs. Upon DSB induction, several factors play roles in chromatin relaxation by catalysing the appropriate histone posttranslational modification (PTM) steps, therefore promoting the access of the repair factors to the DSBs. Among these PTMs, the phosphorylation of the histone variant H2AX at its Ser139 residue (also known as {gamma}H2AX) could be observed at the break sites. The structure of {gamma}H2AX focus has to be organized during the repair as it contributes to accessibility of specific repair proteins to the damaged site. Our aim was to develop a quantitative approach to analyse the morphology of individual repair foci by super-resolution dSTORM microscopy to gain insight into genome organization in DNA repair. We have established a specific dSTORM measurement process by developing a new analytical algorithm for gaining quantitative information about chromatin morphology and repair foci topology at individual {gamma}H2AX enriched repair focus. By this method we quantified unique repair foci to show the average distribution of {gamma}H2AX clusters. By monitoring {gamma}H2AX signal, we could reach 20 nm spatial resolution and resolve a single DNA damage spot, which allow us to identify different chromatin sub-clusters around the break site. Additionally, based on our new analysis method, we were able to show the number of nucleosomes in each sub-cluster that could allow us to define the possible chromatin structure and the nucleosome density around the break sites. This method is the first demonstration of a single-cell based quantitative measurement of a discrete repair focus, which could provide new opportunities to categorize spatial organization of dot patterns by parametric determination of topological similarity.

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Varga, D., Majoros, H., Ujfaludi, Z., Erdelyi, M., Pankotai, T.. 2019-05-14. Quantification of DNA damage induced γH2AX focus formation via super-resolution dSTORM localization microscopy. https://doi.org/10.1101/638361

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