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AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair

Double-strand breaks (DSBs) are the most lethal DNA damages induced by ionising radiation (IR) and their efficient repair is crucial to limit genomic instability. The cellular DSB response after low IR doses is of particular interest but its examination requires the analysis of high cell numbers. He...

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Autores principales: Lengert, Nicor, Mirsch, Johanna, Weimer, Ratna N., Schumann, Eik, Haub, Peter, Drossel, Barbara, Löbrich, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251879/
https://www.ncbi.nlm.nih.gov/pubmed/30470760
http://dx.doi.org/10.1038/s41598-018-35660-5
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author Lengert, Nicor
Mirsch, Johanna
Weimer, Ratna N.
Schumann, Eik
Haub, Peter
Drossel, Barbara
Löbrich, Markus
author_facet Lengert, Nicor
Mirsch, Johanna
Weimer, Ratna N.
Schumann, Eik
Haub, Peter
Drossel, Barbara
Löbrich, Markus
author_sort Lengert, Nicor
collection PubMed
description Double-strand breaks (DSBs) are the most lethal DNA damages induced by ionising radiation (IR) and their efficient repair is crucial to limit genomic instability. The cellular DSB response after low IR doses is of particular interest but its examination requires the analysis of high cell numbers. Here, we present an automated DSB quantification method based on the analysis of γH2AX and 53BP1 foci as markers for DSBs. We establish a combination of object properties, combined in the object evaluation parameter (OEP), which correlates with manual object classification. Strikingly, OEP histograms show a bi-modal distribution with two maxima and a minimum in between, which correlates with the manually determined transition between background signals and foci. We used algorithms to detect the minimum, thus separating foci from background signals and automatically assessing DSB levels. To demonstrate the validity of this method, we analyzed over 600.000 cells to verify results of previous studies showing that DSBs induced by low doses are less efficiently repaired compared with DSBs induced by higher doses. Thus, the automated foci counting method, called AutoFoci, provides a valuable tool for high-throughput image analysis of thousands of cells which will prove useful for many biological screening approaches.
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spelling pubmed-62518792018-11-29 AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair Lengert, Nicor Mirsch, Johanna Weimer, Ratna N. Schumann, Eik Haub, Peter Drossel, Barbara Löbrich, Markus Sci Rep Article Double-strand breaks (DSBs) are the most lethal DNA damages induced by ionising radiation (IR) and their efficient repair is crucial to limit genomic instability. The cellular DSB response after low IR doses is of particular interest but its examination requires the analysis of high cell numbers. Here, we present an automated DSB quantification method based on the analysis of γH2AX and 53BP1 foci as markers for DSBs. We establish a combination of object properties, combined in the object evaluation parameter (OEP), which correlates with manual object classification. Strikingly, OEP histograms show a bi-modal distribution with two maxima and a minimum in between, which correlates with the manually determined transition between background signals and foci. We used algorithms to detect the minimum, thus separating foci from background signals and automatically assessing DSB levels. To demonstrate the validity of this method, we analyzed over 600.000 cells to verify results of previous studies showing that DSBs induced by low doses are less efficiently repaired compared with DSBs induced by higher doses. Thus, the automated foci counting method, called AutoFoci, provides a valuable tool for high-throughput image analysis of thousands of cells which will prove useful for many biological screening approaches. Nature Publishing Group UK 2018-11-23 /pmc/articles/PMC6251879/ /pubmed/30470760 http://dx.doi.org/10.1038/s41598-018-35660-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lengert, Nicor
Mirsch, Johanna
Weimer, Ratna N.
Schumann, Eik
Haub, Peter
Drossel, Barbara
Löbrich, Markus
AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title_full AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title_fullStr AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title_full_unstemmed AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title_short AutoFoci, an automated high-throughput foci detection approach for analyzing low-dose DNA double-strand break repair
title_sort autofoci, an automated high-throughput foci detection approach for analyzing low-dose dna double-strand break repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251879/
https://www.ncbi.nlm.nih.gov/pubmed/30470760
http://dx.doi.org/10.1038/s41598-018-35660-5
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