Caggese C, Caizzi R, Bozzetti M P, Barsanti P, Ritossa F
Istituto di Genetica dell'Università, Bari, Italy.
Biochem Genet. 1988 Oct;26(9-10):571-84. doi: 10.1007/BF02399602.
Recombinational and deletion mapping of electrophoretic variants of the glutamine synthetase I isozyme (GSI) in Drosophila melanogaster locates the gene in the 21B region on the second chromosome. We have conducted a genetic analysis of the region extending cytologically from 21A to 21B4-6. Recessive lethal mutations were generated by ethyl methanesulfonate (EMS) and ethyl nitrosourea (ENU) mutagenesis and by hybrid dysgenesis (HD). These lethals fall into seven functional groups, which were partially ordered by complementation with cytologically defined deficiencies of this region generated by hybrid dysgenesis. Two of the EMS- and two of the ENU-induced lethals fulfill biochemical criteria expected for null alleles of the GSI gene.
对黑腹果蝇谷氨酰胺合成酶I同工酶(GSI)电泳变体进行的重组和缺失图谱分析,将该基因定位在第二条染色体的21B区域。我们对从细胞学上21A延伸到21B4 - 6的区域进行了遗传分析。通过甲磺酸乙酯(EMS)、亚硝酸乙酯(ENU)诱变以及杂种不育(HD)产生隐性致死突变。这些致死突变分为七个功能组,通过与杂种不育产生的该区域细胞学定义的缺失进行互补分析,对这些功能组进行了部分排序。其中两个EMS诱导的致死突变和两个ENU诱导的致死突变符合GSI基因无效等位基因预期的生化标准。