Harrison D A, Geyer P K, Spana C, Corces V G
Department of Biology, Johns Hopkins University, Baltimore, MD 21218.
Dev Genet. 1989;10(3):239-48. doi: 10.1002/dvg.1020100313.
We have used the yellow gene of Drosophila melanogaster as a model system in which to study the molecular mechanisms by which the gypsy retrotransposon causes mutant phenotypes that can be reversed by nonallelic mutations at the suppressor of Hairy-wing locus. This gene encodes a 109,000 dalton protein that contains an acidic domain and 12 copies of the Zn finger motif, which are characteristic of some transcription factors and DNA binding proteins. The suppressible y2 allele is caused by the insertion of the gypsy element at -700 bp from the start of transcription of the yellow gene, resulting in a phenotype characterized by mouth parts and denticle belts in the larvae, and by bristles in the adults, that show wildtype coloration, but mutant wings and body cuticle in the adult flies. This phenotype is the result of the interaction of gypsy sequences homologous to mammalian enhancers with tissue-specific yellow transcriptional regulatory elements located upstream from the gypsy insertion site and responsible for the expression of the yellow gene in the mutated tissues. This interaction is dependent on the binding of the su(Hw) protein to the specific gypsy sequences involved in the induction of the mutant phenotype.
我们使用黑腹果蝇的黄色基因作为一个模型系统,用以研究gypsy逆转录转座子导致突变表型的分子机制,这些突变表型可被毛翅抑制位点的非等位突变所逆转。该基因编码一种109,000道尔顿的蛋白质,它含有一个酸性结构域和12个锌指基序拷贝,这是一些转录因子和DNA结合蛋白的特征。可抑制的y2等位基因是由gypsy元件插入到黄色基因转录起始点上游-700 bp处引起的,导致幼虫的口器和齿带以及成虫的刚毛呈现野生型颜色,但成虫的翅膀和体表角质层呈现突变表型。这种表型是与哺乳动物增强子同源的gypsy序列与位于gypsy插入位点上游且负责黄色基因在突变组织中表达的组织特异性黄色转录调控元件相互作用的结果。这种相互作用依赖于su(Hw)蛋白与诱导突变表型所涉及的特定gypsy序列的结合。