A total of 153 hprt mutants (23 spontaneous, 130 γ-ray-induced) of primary human skin fibroblasts were isolated and genetic alterations at the locus were studied by multiplex polymerase chain reaction (PCR). The analyses showed that 51% (66/130) of ?-ray-induced genetic changes were large deletions, whereas the majority of spontaneous mutants (21/23) exhibited point mutations. The spectrum of large genetic alterations appeared to be dependent on dose in γ-ray-induced (1-4 Gy) mutations; mutants with complete loss of the hprt locus comprised 21 (3/14) or 39% (15/38) of clones isolated after irradiation with 1 or 4 Gy, respectively. The frequency of partial deletions was found to be higher in the mutants isolated from clones irradiated with 2 Gy (38%) than from those irradiated with 4 Gy (8%). Mapping of all intragenic deletion breakpoints exhibited a nonrandom distribution of breakpoints toward the 3′ end of the hprt gene.
Molecular Analysis of Gamma-Ray-Induced Mutations at the hprt Locus in Primary Human Skin Fibroblasts by Multiplex Polymerase Chain Reaction
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Min S. Park, Tracy Hanks, Armin Jaberaboansari, David J. Chen; Molecular Analysis of Gamma-Ray-Induced Mutations at the hprt Locus in Primary Human Skin Fibroblasts by Multiplex Polymerase Chain Reaction. Radiat Res 1 January 1995; 141 (1): 11–18. doi: https://doi.org/10.2307/3579084
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