McLean C, Bucheton A, Finnegan D J
Institute of Cell and Molecular Biology, University of Edinburgh, Scotland.
Mol Cell Biol. 1993 Feb;13(2):1042-50. doi: 10.1128/mcb.13.2.1042-1050.1993.
The I-R system of hybrid dysgenesis in Drosophila melanogaster is controlled by a long interspersed nuclear element-like retroposon, the I factor. Transposition of the I factor occurs at a high frequency only in the ovaries of females produced by crossing males of inducer strains that contain functional I factors with females of reactive strains that lack them. In this study, the 5' untranslated region of the I factor was joined to the chloramphenicol acetyltransferase gene, and activity was assayed in transfected D. melanogaster tissue culture cells and transformed flies. The results have identified a promoter that lies within the first 186 pb of the I factor. Deletion analysis shows that nucleotides +1 to +40 are sufficient for high promoter activity and accurate transcription initiation. This region contains sequences that are found in a class of RNA polymerase II promoters that lack both a TATA box and CpG-rich motifs. In transformed flies, high levels of expression from nucleotides +1 to +186 are confined to the ovaries of reactive females, suggesting that the promoter is involved in the tissue and cytotype specificity of transposition.
果蝇杂交不育的I-R系统由一种长散在核元件样逆转座子I因子控制。I因子的转座仅在含有功能性I因子的诱导株雄性与缺乏I因子的反应株雌性杂交产生的雌性果蝇卵巢中高频发生。在本研究中,将I因子的5'非翻译区与氯霉素乙酰转移酶基因连接,并在转染的果蝇组织培养细胞和转化果蝇中检测活性。结果鉴定出一个位于I因子前186个碱基对以内的启动子。缺失分析表明,核苷酸+1至+40足以实现高启动子活性和准确的转录起始。该区域包含在一类既缺乏TATA盒又缺乏富含CpG基序的RNA聚合酶II启动子中发现的序列。在转化果蝇中,核苷酸+1至+186的高水平表达仅限于反应性雌性果蝇的卵巢,这表明该启动子参与了转座的组织和细胞类型特异性。