Autosomal Mutations in Mouse Kidney Epithelial Cells Exposed to High-Energy Protons In Vivo or In Culture

• Published in: Radiation research Vol. 179; no. 5; pp. 521 - 529
• Main Authors: Turker, Mitchell S., Grygoryev, Dmytro, Dan, Cristian, Eckelmann, Bradley, Lasarev, Michael, Gauny, Stacey, Kwoh, Ely, Kronenberg, Amy
• Format: Journal Article
• Language: English
• Published: United States The Radiation Research Society 01.05.2013; Radiation Research Society; Allen Press Inc
• Subjects: Adenine Phosphoribosyltransferase - genetics; Animals; Cell Line; Cell lines; Chromosome translocation; Chromosomes; Chromosomes, Mammalian - genetics; Chromosomes, Mammalian - radiation effects; Deoxyribonucleic acid; DNA; Dose-Response Relationship, Radiation; Epithelial cells; Epithelial Cells - cytology; Epithelial Cells - metabolism; Epithelial Cells - radiation effects; Female; Genetic Loci - genetics; Genetic Loci - radiation effects; Genetic mutation; Kidney cells; Kidneys; Loss of heterozygosity; Male; Mice; Microenvironments; Mitotic recombination; Mutants; Mutation; Mutation - radiation effects; Protons; Protons - adverse effects; REGULAR ARTICLES
• ISSN: 0033-7587; 1938-5404
• DOI: 10.1667/RR3174.1

Proton exposure induces mutations and cancer, which are presumably linked. Because protons are abundant in the space environment and significant uncertainties exist for the effects of space travel on human health, the purpose of this study was to identify the types of mutations induced by exposure of mammalian cells to 4–5 Gy of 1 GeV protons. We used an assay that selects for mutations affecting the chromosome 8-encoded Aprt locus in mouse kidney cells and selected mutants after proton exposure both in vivo and in cell culture. A loss of heterozygosity (LOH) assay for DNA preparations from the in vivo-derived kidney mutants revealed that protons readily induced large mutational events. Fluorescent in situ hybridization painting for chromosome 8 showed that >70% of proton-induced LOH patterns resembling mitotic recombination were in fact the result of nonreciprocal chromosome translocations, thereby demonstrating an important role for DNA double-strand breaks in proton mutagenesis. Large interstitial deletions, which also require the formation and resolution of double-strand breaks, were significantly induced in the cell culture environment (14% of all mutants), but to a lesser extend in vivo (2% of all mutants) suggesting that the resolution of proton-induced double-strand breaks can differ between the intact tissue and cell culture microenvironments. In total, the results demonstrate that double-strand break formation is a primary determinant for proton mutagenesis in epithelial cell types and suggest that resultant LOH for significant genomic regions play a critical role in proton-induced cancers.