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Title: The genome-wide effects of ionizing radiation on mutation induction in the mammalian germline.
Authors: Adewoye, Adeolu B.
Lindsay, S. J.
Dubrova, Yuri E.
Hurles, M. E.
First Published: 26-Mar-2015
Publisher: Nature Publishing Group
Citation: Nature Communications, 2015, 6, pp. 6684-?
Abstract: The ability to predict the genetic consequences of human exposure to ionizing radiation has been a long-standing goal of human genetics in the past 50 years. Here we present the results of an unbiased, comprehensive genome-wide survey of the range of germline mutations induced in laboratory mice after parental exposure to ionizing radiation and show irradiation markedly alters the frequency and spectrum of de novo mutations. Here we show that the frequency of de novo copy number variants (CNVs) and insertion/deletion events (indels) is significantly elevated in offspring of exposed fathers. We also show that the spectrum of induced de novo single-nucleotide variants (SNVs) is strikingly different; with clustered mutations being significantly over-represented in the offspring of irradiated males. Our study highlights the specific classes of radiation-induced DNA lesions that evade repair and result in germline mutation and paves the way for similarly comprehensive characterizations of other germline mutagens.
DOI Link: 10.1038/ncomms7684
eISSN: 2041-1723
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit
Description: Accession codes: The microarray data were deposited in the Gene Expression Omnibus (GEO), submission number GSE65521; the whole-genome sequences were deposited in the Sequence Read Archive under Study number ERP001221, with accession numbers ERX111346, ERX111347, ERX111348, ERX111349, ERX111350, ERX111351, ERX111352, ERX111353, ERX111354, ERX111355, ERX111356, ERX111357, ERX111358, ERX111359, ERX111360, ERX111361, ERX111362, ERX111363, ERX111364, ERX111365, ERX111366 and ERX111367. Supplementary Information accompanies this paper at
Appears in Collections:Published Articles, Dept. of Genetics

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