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Genetic analysis of enhancer of split, a locus involved in neurogenesis in Drosophila melanogaster.

机译:分裂增强子的遗传学分析,该分裂子是果蝇中神经发生的一个位点。

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Enhancer of split (E(spl)), one of the neurogenic loci of Drosophila, is uncovered by the deletion Df(3R)E(spl)(R-B251) with breakpoints at 96F8 and 96F13. We describe here the results of a genetic analysis of this chromosomal interval. Thirty-one mutations in genes of this region were recovered during various programs of mutagenesis. In addition, we included the spontaneous mutations E(spl)(D) and groucho (gro), which are known to map to this region, in our study. These 33 mutations define four lethal complementation groups, one of which includes E(spl)(D) and gro. Mutations of the E(spl) group behave as complementing and noncomplementing pseudoalleles, defining different functions. Alleles are classified according to their complementation behavior in two different ways: with respect to their viability as heterozygotes with other lethal alleles and with respect to gro and to E(spl)(D). The phenotypes of these mutations and the pattern of heteroallelic complementation speak in favor of a considerable genetic complexity of the E(spl) locus.
机译:果蝇的神经原性基因座之一的分裂增强子(E(spl))未通过在96F8和96F13处具有断点的Df(3R)E(spl)(R-B251)缺失发现。我们在此描述此染色体区间的遗传分析结果。在各种诱变程序中恢复了该区域基因的31个突变。此外,在我们的研究中,我们包括了自发突变E(spl)(D)和groucho(gro),这些突变已知映射到该区域。这33个突变定义了四个致命的互补组,其中一个包括E(spl)(D)和gro。 E(spl)组的突变表现为互补和非互补伪等位基因,定义了不同的功能。等位基因根据它们的互补行为以两种不同的方式进行分类:就其与其他致死等位基因作为杂合子的生存力而言,以及针对gro和E(spl)(D)而言。这些突变的表型和异源等位基因互补的模式表明,E(spl)基因座的遗传复杂性很高。

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