Roiha H, Rubin G M, O'Hare K
Department of Biochemistry, University of California, Berkeley 94720.
Genetics. 1988 May;119(1):75-83. doi: 10.1093/genetics/119.1.75.
DNA from the singed gene of Drosophila melanogaster was isolated using an inversion between a previously cloned P element at cytological location 17C and the hypermutable allele singed-weak. Five out of nine singed mutants examined have alterations in their DNA maps in this region. The singed locus is a hotspot for mutation during P-M hybrid dysgenesis, and we have analyzed 22 mutations induced by P-M hybrid dysgenesis. All 22 have a P element inserted within a 700-bp region. The precise positions of 10 P element insertions were determined and they define 4 sites within a 100-bp interval. During P-M hybrid dysgenesis, the singed-weak allele is destabilized, producing two classes of phenotypically altered derivatives at high frequency. In singed-weak, two defective P elements are present in a "head-to-head" or inverse tandem arrangement. Excision of one element results in a more extreme singed bristle phenotype while excision of the other leads to a wild-type bristle phenotype.
利用位于细胞学位置17C的一个先前克隆的P因子与高突变等位基因焦刚毛-弱之间的倒位,分离出了黑腹果蝇焦刚毛基因的DNA。在检测的9个焦刚毛突变体中,有5个在该区域的DNA图谱上存在改变。焦刚毛位点是P-M杂种不育过程中的一个突变热点,我们分析了22个由P-M杂种不育诱导产生的突变。所有22个突变都有一个P因子插入在一个700碱基对的区域内。确定了10个P因子插入的精确位置,它们在一个100碱基对的间隔内定义了4个位点。在P-M杂种不育过程中,焦刚毛-弱等位基因不稳定,高频产生两类表型改变的衍生物。在焦刚毛-弱中,两个有缺陷的P因子以“头对头”或反向串联排列存在。切除其中一个因子会导致更极端的焦刚毛表型,而切除另一个则会导致野生型刚毛表型。