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检测CD-1雄性小鼠F1代子代中经三乙撑亚胺诱导产生的相互易位:连续生育力评估与细胞遗传学分析的比较

Detection of TEM-induced reciprocal translocations in F1 sons of CD-1 male mice: comparison of sequential fertility evaluation and cytogenetic analysis.

作者信息

Morris S M, Kodell R L, Domon O E, Bishop J B

机构信息

Department of Health and Human Services, Food and Drug Administration, Jefferson, Arkansas.

出版信息

Environ Mol Mutagen. 1988;11(2):215-23. doi: 10.1002/em.2850110207.

Abstract

To determine the positive and negative classification error rates associated with the HTA in our laboratory, F1 sons of TEM-exposed CD-1 male mice were evaluated by the sequential fertility method with subsequent cytogenetic analysis. Males who sired three litters of size 10 or less when mated to primiparous females from either the B6C3F1 or the BCF1 strain were classified as partial steriles. When meiotic chromosome analyses revealed the presence of at least two cells containing multivalent figures, males were classified as translocation heterozygotes. When the fertility evaluation and the cytogenetic analysis were compared, normal fertility was observed on 5 of 83 (6.02%) translocation-bearing F1 males mated to B6C3F1 tester females and on 3 of 83 (3.61%) F1 males mated to BCF1 tester females. Thus, the false-negative error rates were 6.02% and 3.61% with these two tester strains. Multivalent figures were not observed in the meiotic chromosomes of 410 F1 males. Of these, 12 (2.93%) had reduced fertility when mated to the B6C3F1 tester strain as did 7 (1.71%) mated to the BCF1 strain. Thus, the false-positive error rates with these two tester strains were 2.93% for the B6C3F1 strain and 1.71% for the BCF1 strain. Our results indicate that non-zero error rates, both false-positive and false-negative, are associated with the sequential mating method HTA. In addition, the magnitude of these error rates was influenced not only by the tester female strain but also by the genotype of the F1 male.

摘要

为确定我们实验室中与杂交试验分析法(HTA)相关的阳性和阴性分类错误率,对经三乙撑四胺(TEM)处理的CD-1雄性小鼠的F1代雄性后代采用连续生育力方法进行评估,并随后进行细胞遗传学分析。当与B6C3F1或BCF1品系的初产雌性小鼠交配时,产仔三窝且每窝大小为10只或更少的雄性被分类为部分不育。当减数分裂染色体分析显示存在至少两个含有多价体图形的细胞时,雄性被分类为易位杂合子。当比较生育力评估和细胞遗传学分析时,在与B6C3F1测试雌性小鼠交配的83只携带易位的F1雄性小鼠中有5只(6.02%)观察到正常生育力,在与BCF1测试雌性小鼠交配的83只F1雄性小鼠中有3只(3.61%)观察到正常生育力。因此,这两种测试品系的假阴性错误率分别为6.02%和3.61%。在410只F1雄性小鼠的减数分裂染色体中未观察到多价体图形。其中,与B6C3F1测试品系交配时,有12只(2.93%)生育力降低;与BCF1品系交配时,有7只(1.71%)生育力降低。因此,这两种测试品系的假阳性错误率,对于B6C3F1品系为2.93%,对于BCF1品系为1.71%。我们的结果表明,杂交试验分析法(HTA)的连续交配方法存在非零的假阳性和假阴性错误率。此外,这些错误率的大小不仅受测试雌性品系的影响,还受F1雄性基因型的影响。

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