Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/24799
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dc.contributor.authorMoorhouse, AJ-
dc.contributor.authorScholze, M-
dc.contributor.authorSylvius, N-
dc.contributor.authorGilham, C-
dc.contributor.authorRake, C-
dc.contributor.authorPeto, J-
dc.contributor.authorAnderson, R-
dc.contributor.authorDubrova, YE-
dc.date.accessioned2022-07-05T12:48:07Z-
dc.date.available2022-07-05T12:48:07Z-
dc.date.issued2022-07-05-
dc.identifier10830-
dc.identifier.citationMoorhouse, A.J., Scholze, M., Sylvius, N., Gilham, C., Rake, C., Peto, J., Anderson, R. and Dubrova, Y.E. (2022) 'No evidence of increased mutations in the germline of a group of British nuclear test veterans', Scientific Reports, 12, 10830, pp. 1-8. doi: 10.1038/s41598-022-14999-w.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/24799-
dc.descriptionAvailability of data and materials: The dataset generated during this current study are available https://dataview.ncbi.nlm.nih.gov/object/PRJNA788492?reviewer=t65okctpc20o0jfr3n2rmf5n50en_US
dc.descriptionEthical Approval and consent to participate: The GCFT study was conducted in accordance with UK ethical framework and approved by the UK Health Research Authority (17/LO/0273).-
dc.description.abstractCopyright © The Author(s) 2022. The potential germline effects of radiation exposure to military veterans present at British nuclear tests in Australia and the South Pacific is of considerable interest. We analyzed germline mutations in 60 families of UK military personnel comprising 30 control and 30 nuclear test veterans (NTV). Using whole-genome sequencing we studied the frequency and spectra of de novo mutations to investigate the transgenerational effect of veterans’ (potential) exposure to radiation at nuclear bomb test sites. We find no elevation in total de novo single nucleotide variants, small insertion-deletions, structural variants or clustered mutations among the offspring of nuclear test veterans compared to those of control personnel. We did observe an elevated occurrence of single base substitution mutations within mutation signature SBS16, due to a subset of NTV offspring. The relevance of this elevation to potential exposure of veteran fathers and, future health risks, require further investigation. Overall, we find no evidence of increased mutations in the germline of a group of British nuclear test veterans. ISRCTN Registry 17461668.-
dc.description.sponsorshipNuclear Community Charity Fund (NCCF) through funds received by The Armed Forces Covenant Fund Trust under the Aged Veterans Fund Grant AVF16 (AM, MS, CG, CR, JP, RA, YD).en_US
dc.format.extent1 - 8-
dc.format.mediumElectronic-
dc.language.isoen_USen_US
dc.publisherSpringer Natureen_US
dc.rightsCopyright © The Author(s) 2022. Rights and permissions: 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit https://creativecommons.org/licenses/by/4.0/.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectde novo DNA mutationsen_US
dc.subjectwhole genome sequence analysisen_US
dc.subjectgermlineen_US
dc.subjectionizing radiationen_US
dc.subjecthuman populationen_US
dc.titleNo evidence of increased mutations in the germline of a group of British nuclear test veteransen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1038/s41598-022-14999-w-
dc.relation.isPartOfScientific Reports-
pubs.publication-statusPublished-
pubs.volume12-
dc.identifier.eissn2045-2322-
dc.rights.holderThe Author(s)-
Appears in Collections:Dept of Life Sciences Research Papers

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