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Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation

A genome-wide evaluation of the effects of ionizing radiation on mutation induction in the mouse germline has identified multisite de novo mutations (MSDNs) as marker for previous exposure. Here we present the results of a small pilot study of whole genome sequencing in offspring of soldiers who ser...

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Autores principales: Holtgrewe, Manuel, Knaus, Alexej, Hildebrand, Gabriele, Pantel, Jean-Tori, Santos, Miguel Rodriguez de los, Neveling, Kornelia, Goldmann, Jakob, Schubach, Max, Jäger, Marten, Coutelier, Marie, Mundlos, Stefan, Beule, Dieter, Sperling, Karl, Krawitz, Peter Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168503/
https://www.ncbi.nlm.nih.gov/pubmed/30279461
http://dx.doi.org/10.1038/s41598-018-33066-x
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author Holtgrewe, Manuel
Knaus, Alexej
Hildebrand, Gabriele
Pantel, Jean-Tori
Santos, Miguel Rodriguez de los
Neveling, Kornelia
Goldmann, Jakob
Schubach, Max
Jäger, Marten
Coutelier, Marie
Mundlos, Stefan
Beule, Dieter
Sperling, Karl
Krawitz, Peter Michael
author_facet Holtgrewe, Manuel
Knaus, Alexej
Hildebrand, Gabriele
Pantel, Jean-Tori
Santos, Miguel Rodriguez de los
Neveling, Kornelia
Goldmann, Jakob
Schubach, Max
Jäger, Marten
Coutelier, Marie
Mundlos, Stefan
Beule, Dieter
Sperling, Karl
Krawitz, Peter Michael
author_sort Holtgrewe, Manuel
collection PubMed
description A genome-wide evaluation of the effects of ionizing radiation on mutation induction in the mouse germline has identified multisite de novo mutations (MSDNs) as marker for previous exposure. Here we present the results of a small pilot study of whole genome sequencing in offspring of soldiers who served in radar units on weapon systems that were emitting high-frequency radiation. We found cases of exceptionally high MSDN rates as well as an increased mean in our cohort: While a MSDN mutation is detected in average in 1 out of 5 offspring of unexposed controls, we observed 12 MSDNs in altogether 18 offspring, including a family with 6 MSDNs in 3 offspring. Moreover, we found two translocations, also resulting from neighboring mutations. Our findings indicate that MSDNs might be suited in principle for the assessment of DNA damage from ionizing radiation also in humans. However, as exact person-related dose values in risk groups are usually not available, the interpretation of MSDNs in single families would benefit from larger molecular epidemiologic studies on this new biomarker.
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spelling pubmed-61685032018-10-05 Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation Holtgrewe, Manuel Knaus, Alexej Hildebrand, Gabriele Pantel, Jean-Tori Santos, Miguel Rodriguez de los Neveling, Kornelia Goldmann, Jakob Schubach, Max Jäger, Marten Coutelier, Marie Mundlos, Stefan Beule, Dieter Sperling, Karl Krawitz, Peter Michael Sci Rep Article A genome-wide evaluation of the effects of ionizing radiation on mutation induction in the mouse germline has identified multisite de novo mutations (MSDNs) as marker for previous exposure. Here we present the results of a small pilot study of whole genome sequencing in offspring of soldiers who served in radar units on weapon systems that were emitting high-frequency radiation. We found cases of exceptionally high MSDN rates as well as an increased mean in our cohort: While a MSDN mutation is detected in average in 1 out of 5 offspring of unexposed controls, we observed 12 MSDNs in altogether 18 offspring, including a family with 6 MSDNs in 3 offspring. Moreover, we found two translocations, also resulting from neighboring mutations. Our findings indicate that MSDNs might be suited in principle for the assessment of DNA damage from ionizing radiation also in humans. However, as exact person-related dose values in risk groups are usually not available, the interpretation of MSDNs in single families would benefit from larger molecular epidemiologic studies on this new biomarker. Nature Publishing Group UK 2018-10-02 /pmc/articles/PMC6168503/ /pubmed/30279461 http://dx.doi.org/10.1038/s41598-018-33066-x 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
Holtgrewe, Manuel
Knaus, Alexej
Hildebrand, Gabriele
Pantel, Jean-Tori
Santos, Miguel Rodriguez de los
Neveling, Kornelia
Goldmann, Jakob
Schubach, Max
Jäger, Marten
Coutelier, Marie
Mundlos, Stefan
Beule, Dieter
Sperling, Karl
Krawitz, Peter Michael
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title_full Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title_fullStr Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title_full_unstemmed Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title_short Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
title_sort multisite de novo mutations in human offspring after paternal exposure to ionizing radiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168503/
https://www.ncbi.nlm.nih.gov/pubmed/30279461
http://dx.doi.org/10.1038/s41598-018-33066-x
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