Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/13412
Title: DNMTs are required for delayed genome instability caused by radiation
Authors: Armstrong, Christine A.
Jones, George D.
Anderson, R.
Pooja, Iyer
Narayanan, Deepan
Sandhu, Jatinderpal
Singh, Rajinder
Talbot, Christopher J.
Tufarelli, C
First Published: 22-Jul-2012
Publisher: Taylor & Francis for Epigenetics Society, Landes Bioscience
Citation: Epigenetics, 2012, 7 (8), pp. 892-902
Abstract: The ability of ionizing radiation to initiate genomic instability has been harnessed in the clinic where the localized delivery of controlled doses of radiation is used to induce cell death in tumor cells. Though very effective as a therapy, tumor relapse can occur in vivo and its appearance has been attributed to the radio-resistance of cells with stem cell-like features. The molecular mechanisms underlying these phenomena are unclear but there is evidence suggesting an inverse correlation between radiation-induced genomic instability and global hypomethylation. To further investigate the relationship between DNA hypomethylation, radiosensitivity and genomic stability in stem-like cells we have studied mouse embryonic stem cells containing differing levels of DNA methylation due to the presence or absence of DNA methyltransferases. Unexpectedly, we found that global levels of methylation do not determine radiosensitivity. In particular, radiation-induced delayed genomic instability was observed at the Hprt gene locus only in wild-type cells. Furthermore, absence of Dnmt1 resulted in a 10-fold increase in de novo Hprt mutation rate, which was unaltered by radiation. Our data indicate that functional DNMTs are required for radiation-induced genomic instability, and that individual DNMTs play distinct roles in genome stability. We propose that DNMTS may contribute to the acquirement of radio-resistance in stem-like cells.
DOI Link: 10.4161/epi.21094
ISSN: 1559-2294
eISSN: 1559-2308
Links: http://hdl.handle.net/2381/13412
http://www.tandfonline.com/doi/abs/10.4161/epi.21094
Type: Journal Article
Rights: Copyright © 2012 Landes Bioscience This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
Appears in Collections:Published Articles, Dept. of Genetics

Files in This Item:
File Description SizeFormat 
epi%2E21094.pdfPublisher version1.35 MBAdobe PDFView/Open


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.