Jürgens G, Wieschaus E, Nüsslein-Volhard C, Kluding H
European Molecular Biology Laboratory, D-6900, Heidelberg, Federal Republic of Germany.
Friedrich-Miescher-Laboratorium der Max-Planck-Gesellschaft, Spemannstrasse 37-39, D-7400, Tübingen, Federal Republic of Germany.
Wilehm Roux Arch Dev Biol. 1984 Sep;193(5):283-295. doi: 10.1007/BF00848157.
The present report describes the recovery and genetic characterization of mutant alleles at zygotic loci on the third chromosome ofDrosophila melanogaster which alter the morphology of the larval cuticle. We derived 12600 single lines from ethyl methane sulfonate (EMS)-treatedst e orrucuca chromosomes and assayed them for embryonic lethal mutations by estimating hatch rates of egg collections. About 7100 of these lines yielded at least a quarter of unhatched eggs and were then scored for embryonic phenotypes. Through microscopic examination of unhatched eggs 1772 lines corresponding to 24% of all lethal hits were classified as embryonic lethal. In 198 lines (2.7% of all lethal hits), mutant embryos showed distinct abnormalities of the larval cuticle. These embryonic visible mutants define 45 loci by complementation analysis. For 32 loci, more than one mutant allele was recovered, with an average of 5.8 alleles per locus. Complementation of all other mutants was shown by 13 mutants. The genes were localized on the genetic map by recombination analysis, as well as cytologically by complementation analysis with deficiencies. They appear to be randomly distributed along the chromosome. Allele frequencies and comparisons with deficiency phenotypes indicate that the 45 loci represent most, if not all, zygotic loci on the third chromosome, where lack of function recognizably affects the morphology of the larval cuticle.
本报告描述了黑腹果蝇第三染色体合子基因座上改变幼虫表皮形态的突变等位基因的恢复和遗传特征。我们从经甲基磺酸乙酯(EMS)处理的st e orrucuca染色体中获得了12600个单系,并通过估计卵收集的孵化率来检测它们是否存在胚胎致死突变。这些品系中约有7100个产生了至少四分之一未孵化的卵,然后对其胚胎表型进行评分。通过对未孵化卵的显微镜检查,1772个品系(占所有致死突变的24%)被归类为胚胎致死。在198个品系(占所有致死突变的2.7%)中,突变胚胎表现出幼虫表皮的明显异常。通过互补分析,这些胚胎可见突变体定义了45个基因座。对于32个基因座,回收了不止一个突变等位基因,每个基因座平均有5.8个等位基因。13个突变体显示了所有其他突变体的互补情况。通过重组分析以及与缺失的互补分析在细胞学上对这些基因进行了定位。它们似乎沿染色体随机分布。等位基因频率以及与缺失表型的比较表明,这45个基因座代表了第三染色体上大部分(如果不是全部)合子基因座,在这些基因座上功能缺失明显影响幼虫表皮的形态。