Cellular and molecular analysis of mutagenesis induced by charged particles of defined linear energy transfer

• Published in: Radiation research Vol. 145; no. 3; p. 251
• Main Authors: Zhu, L X, Waldren, C A, Vannias, D, Hei, T K
• Format: Journal Article
• Language: English
• Published: United States 01.03.1996
• Subjects: Animals; Cell Survival - radiation effects; CHO Cells; Chromosome Deletion; Cloning, Molecular; Cricetinae; DNA - radiation effects; Dose-Response Relationship, Radiation; Gamma Rays; Genotype; Humans; Hybrid Cells - radiation effects; Hypoxanthine Phosphoribosyltransferase - genetics; Hypoxanthine Phosphoribosyltransferase - radiation effects; Linear Energy Transfer; Mutagenesis; Polymerase Chain Reaction; NASA Discipline Radiation Health; Non-NASA Center
• ISSN: 0033-7587
• DOI: 10.2307/3578979

Mutation induction by charged particles of defined linear energy transfer (LET) and gamma rays was scored using human-hamster hybrid AL cells. The LET values for charged particles accelerated at the Radiological Research Accelerator Facility ranged from 10 keV/microm protons to 150 keV/microm 4He ions. The induced mutant fractions at both the S1 and HGPRT loci were dependent on the dose and LET. In addition, for each dose examined, the mutant yield at the S1 locus was 30-60 fold higher than at the corresponding HGPRT locus. To determine whether the mutation spectrum was comparably dependent on dose and LET, independent S1- and HGPRT- mutants induced by 150 keV/microm 4He ions and gamma rays were isolated, and their DNA was analyzed by both Southern blotting and multiplex PCR methods. While the majority of radiation-induced mutants showed deletions of varying sizes, the relative percentage of large deletions was found to be related to both the dose and LET of the radiation examined. Using a mutation system that can detect multilocus changes, results of the present study show that radiation-induced chromosomal loss can be in the millions of base pairs.