Tiong S Y, Keizer C, Nash D, Bleskan J, Patterson D
Department of Genetics, University of Alberta, Edmonton, Canada.
Biochem Genet. 1989 Jun;27(5-6):333-48. doi: 10.1007/BF00554168.
New mutant alleles of the adenosine2 locus (ade2; 2-17.7) have been isolated using the eye-color phenotype exhibited by the prototype auxotrophic allele ade2 as the screening criterion. The new mutants form a single complementation group, suggesting that they all exhibit purine auxotrophy and defective formylglycineamide ribotide amidotransferase enzyme, like ade2. Tests carried out on particular new alleles confirm these suggestions. The new mutants all exhibit more extreme physical defects than the prototype. They have wing abnormalities like mutants defective in pyrmidine biosynthesis and reduced bristles like those defective in protein synthesis; thus they exhibit the combined visible phenotype of rudimentary wings, rosy eyes, and bobbed bristles. Cytogenetic analysis places the locus in the interband proximal to 26B1-2.
利用原型营养缺陷型等位基因ade2所表现出的眼色表型作为筛选标准,分离出了腺苷2位点(ade2;2-17.7)的新突变等位基因。新突变体形成一个单一的互补群,这表明它们都表现出嘌呤营养缺陷以及与ade2一样的甲酰甘氨酰胺核糖核苷酸酰胺转移酶缺陷。对特定新等位基因进行的测试证实了这些推测。新突变体都表现出比原型更严重的身体缺陷。它们具有类似嘧啶生物合成缺陷的突变体的翅异常,以及类似蛋白质合成缺陷的突变体的刚毛减少;因此,它们表现出残翅、红眼和短刚毛的综合可见表型。细胞遗传学分析将该位点定位在靠近26B1-2的带间区域。