Charles D J, Pretsch W
Mutat Res. 1986 May;160(3):243-8. doi: 10.1016/0027-5107(86)90134-x.
(101/E1 X C3H/E1)F1-hybrid male mice were exposed in a 24-h fractionation interval to either 3.0 + 3.0-Gy or 5.1 + 5.1-Gy X-irradiation, and mated to untreated Test-stock females. The offspring were examined for mutations at 7 recessive specific loci and for activity alterations of erythrocyte enzymes controlled presumably by 12 loci. No enzyme-activity mutant was found in 3610 F1-offspring of the control group. In the experimental groups, no mutant was detected in 533 (3.0 + 3.0 Gy) and 173 (5.1 + 5.1 Gy) offspring from postspermatogonial germ cells treated. After treatment of spermatogonia. I mutant in 3388 F1-offspring of the 3.0 + 3.0-Gy group, and 5 mutants in 3187 F1 offspring of the 5.1 + 5.1-Gy group were found. The mutants were all genetically confirmed. The frequency (expressed as mutants/locus/gamete) of enzyme-activity mutations is 2 (5.1 + 5.1-Gy group) to 10 (3.0 + 3.0-Gy group) times lower than the frequency of recessive specific-locus mutations.
将(101/E1 X C3H/E1)F1杂交雄性小鼠以24小时的分次间隔接受3.0 + 3.0 Gy或5.1 + 5.1 Gy的X射线照射,然后与未处理的试验种群雌性小鼠交配。对后代进行7个隐性特定基因座的突变检查以及对可能由12个基因座控制的红细胞酶活性改变的检查。在对照组的3610只F1后代中未发现酶活性突变体。在实验组中,经精原细胞后处理的533只(3.0 + 3.0 Gy)和173只(5.1 + 5.1 Gy)后代中未检测到突变体。在精原细胞处理后,在3.0 + 3.0 Gy组的3388只F1后代中发现1只突变体,在5.1 + 5.1 Gy组的3187只F1后代中发现5只突变体。这些突变体均经遗传学确认。酶活性突变的频率(以突变体/基因座/配子表示)比隐性特定基因座突变的频率低2倍(5.1 + 5.1 Gy组)至10倍(3.0 + 3.0 Gy组)。