Degelmann A
Institut für Genetik, Heinrich-Heine-Universität Düsseldorf, Germany.
Mol Gen Genet. 1993 May;239(1-2):257-68. doi: 10.1007/BF00281626.
Reversion mutagenesis of three single P elements located in the cytogenetic interval 1E-2A at the tip of the X chromosome of Drosophila melanogaster was used to recover new deletions in this chromosomal region. The deletions obtained include small aberrations within region 2A and larger lesions extending from 2A into 1E and 1B. All three screens also yielded terminal deficiencies. The new deficiencies, together with previously characterized rearrangements, were analyzed for their complementation behaviour with the maternal effect locus fs(1) Nasrat and lethal loci in the region. These analyses provide an overall genetic map of the interval 1E-2A. In addition, the smaller deletions were physically mapped within cloned genomic DNA of the 2A region.
利用位于黑腹果蝇X染色体末端细胞遗传学区间1E - 2A的三个单个P因子的回复突变诱变来恢复该染色体区域区域的新缺失。获得的缺失包括2A区域内的小畸变以及从2A延伸到1E和1B的更大损伤。所有这三个筛选也产生了末端缺失。分析了这些新的缺失以及先前表征的重排与母体效应基因座fs(1)Nasrat和该区域致死基因座的互补行为。这些分析提供了1E - 2A区间的整体遗传图谱。此外,较小的缺失在2A区域的克隆基因组DNA内进行了物理定位。