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AKR、BALB/c、DBA/2和(102xC3H)F1小鼠生殖细胞中辐射诱导的隐性可见突变、显性白内障突变和酶活性等位基因突变频率的估计。

Estimates of the radiation-induced mutation frequencies to recessive visible, dominant cataract and enzyme-activity alleles in germ cells of AKR, BALB/c, DBA/2 and (102xC3H)F1 mice.

作者信息

Pretsch W, Favor J, Lehmacher W, Neuhäuser-Klaus A

机构信息

GSF-Forschungszentrum für Umwelt und Gesundheit GmbH, Institut für Säugetiergenetik, Oberschleissheim, Germany.

出版信息

Mutagenesis. 1994 Jul;9(4):289-94. doi: 10.1093/mutage/9.4.289.

Abstract

Male mice of the genotypes AKR, BALB/c, (102/ElxC3H/El)F1 or DBA/2 were exposed to 3 + 3 Gy irradiation with a 24 h fractionation interval and mated to untreated Test-stock females. The offspring were screened for activity alterations of 10 erythrocyte enzymes as well as recessive specific-locus and dominant cataract mutations. The observed mutation rates per locus per gamete x 10(-5) for treated spermatogonia were 6.8, 4.9, 2.5 and 1.3 for enzyme-activity mutations, 8.6, 24.1, 22.8 and 31.4 for specific-locus mutations, and 0.7, 0.9, 0.6 and 2.5 for cataract mutations, respectively. Some variability from strain to strain in the frequency of radiation-induced mutations was observed. However, there was no consistent effect of genotype on the frequency of induced mutations and it is concluded that no effect of genetic background exists for the four genotypes tested. There is good agreement between the observed enzyme-activity mutation rate in children of survivors of the atomic bombings and the expected mutation rate based on results with mice. Results are therefore consistent with an estimation of human radiation-induced genetic risks based upon an extrapolation of experimental results in the mouse.

摘要

将基因型为AKR、BALB/c、(102/ElxC3H/El)F1或DBA/2的雄性小鼠,以24小时的分次间隔接受3 + 3 Gy的辐照,并与未处理的测试种群雌性小鼠交配。对后代进行10种红细胞酶活性改变以及隐性特定位点和显性白内障突变的筛选。处理后的精原细胞每个基因座每个配子×10(-5)的观察到的突变率,酶活性突变分别为6.8、4.9、2.5和1.3,特定位点突变分别为8.6、24.1、22.8和31.4,白内障突变分别为0.7、0.9、0.6和2.5。观察到辐射诱导突变频率在不同品系间存在一些差异。然而,基因型对诱导突变频率没有一致的影响,得出结论,所测试的四种基因型不存在遗传背景效应。原子弹爆炸幸存者后代中观察到的酶活性突变率与基于小鼠结果预期的突变率之间有很好的一致性。因此,结果与基于小鼠实验结果外推来估计人类辐射诱导的遗传风险是一致的。

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