Graw J, Favor J, Neuhäuser-Klaus A, Ehling U H
Mutat Res. 1986 Jan-Feb;159(1-2):47-54. doi: 10.1016/0027-5107(86)90111-9.
Male mice were X-irradiated with 3.0 + 3.0 Gy or 5.1 + 5.1 Gy (fractionation interval 24 h). The offspring were screened for dominant cataract and recessive specific locus mutations. In the 3.0 + 3.0-Gy spermatogonial treatment group, 3 dominant cataract mutations were confirmed in 15 551 offspring examined and 29 specific locus mutations were recovered in 18 139 offspring. In the post-spermatogonial treatment group, 1 dominant cataract mutation was obtained in 1120 offspring and 1 recessive specific locus mutation was recovered in 1127 offspring. The induced mutation rate per locus, per gamete, per Gy calculated for recessive specific locus mutations is 2.0 X 10(-5) in post-spermatogonial stages and 3.7 X 10(-5) in spermatogonia. For dominant cataract mutations, assuming 30 loci, the induced mutation rate is 5.0 X 10(-6) in the post-spermatogonial stages and 1.1 X 10(-6) in spermatogonia. In the 5.1 + 5.1-Gy spermatogonial treatment group, 3 dominant cataract mutations were obtained in 11 205 offspring, whereas in 13 201 offspring 27 recessive specific locus mutations were detected in the spermatogonial group. In the post-spermatogonial treatment group no dominant cataract mutation was observed in 425 offspring and 2 recessive specific locus mutations were detected in 445 offspring. The induced mutation rate per locus, gamete and Gy in spermatogonia for recessive specific locus mutations is 2.8 X 10(-5) and for dominant cataract mutations 0.9 X 10(-6). In post-spermatogonial stages, the mutation rate for recessive specific locus alleles is 6.2 X 10(-5). In the concurrent untreated control group, in 11 036 offspring no dominant cataract mutation and in 23 518 offspring no recessive specific locus mutation was observed. Litter size and the number of carriers at weaning have been determined in the confirmation crosses of the obtained dominant cataract mutants as indicators of viability and penetrance effects. Two mutants had a statistically significantly reduced litter size and one mutant had a statistically significantly reduced penetrance.
雄性小鼠接受3.0 + 3.0 Gy或5.1 + 5.1 Gy的X射线照射(分次照射间隔24小时)。对其后代进行显性白内障和隐性特定位点突变筛查。在3.0 + 3.0 - Gy精原细胞治疗组中,在检查的15551只后代中确认了3个显性白内障突变,在18139只后代中发现了29个特定位点突变。在精原细胞后治疗组中,在1120只后代中获得了1个显性白内障突变,在1127只后代中发现了1个隐性特定位点突变。针对隐性特定位点突变计算的每个位点、每个配子、每Gy的诱导突变率,在精原细胞后阶段为2.0×10⁻⁵,在精原细胞中为3.7×10⁻⁵。对于显性白内障突变,假设为30个位点,在精原细胞后阶段诱导突变率为5.0×10⁻⁶,在精原细胞中为1.1×10⁻⁶。在5.1 + 5.1 - Gy精原细胞治疗组中,在11205只后代中获得了3个显性白内障突变,而在精原细胞组的13201只后代中检测到27个隐性特定位点突变。在精原细胞后治疗组中,在425只后代中未观察到显性白内障突变,在445只后代中检测到2个隐性特定位点突变。精原细胞中针对隐性特定位点突变的每个位点、配子和Gy的诱导突变率为2.8×10⁻⁵,对于显性白内障突变则为0.9×10⁻⁶。在精原细胞后阶段,隐性特定位点等位基因的突变率为6.2×10⁻⁵。在同期未处理的对照组中,在11036只后代中未观察到显性白内障突变,在23518只后代中未观察到隐性特定位点突变。在获得的显性白内障突变体的确认杂交中,已确定窝仔数和断奶时携带者数量作为活力和外显率效应的指标。两个突变体的窝仔数在统计学上显著减少,一个突变体的外显率在统计学上显著降低。