Investigation of mutational specificity at low doses has generally not
been possible since the number of induced mutants may be similar or s
ignificantly lower than the spontaneous background. The use of a low-d
ose fractionated exposure protocol in TK6 human lymphoblasts results i
n an incremental accumulation of mutants induced by individual 20 cGy
gamma-ray exposures. Therefore, the frequency of induced mutants withi
n a population at the conclusion of a fractionated exposure regimen is
sufficiently elevated to permit the recovery of a low-dose mutant col
lection. Statistical analysis of the data identified no significant di
fferences between mutants induced by 20 or 200 cGy. However, deletions
encompassing one or more Xq26 STS markers flanking the hprt locus rep
resented only 1/107 (0.009) spontaneous HPRT(-) mutants but 34/170 (0.
20) mutants induced by 20 or 200 cGy of ionizing radiation (P < 0.0001
), The data presented here demonstrate that mutational fingerprints ca
n be effectively defined using deletion mapping for clastogens such as
ionizing radiation, and that the radiation-induced mutational spectru
m is independent of dose.