Shirk P D, Bossin H, Furlong R B, Gillett J L
USDA ARS CMAVE, Gainesville, FL 32608, USA.
Insect Mol Biol. 2007 Oct;16(5):623-33. doi: 10.1111/j.1365-2583.2007.00759.x. Epub 2007 Aug 22.
Transcriptional activity of the Junonia coenia densovirus (JcDNV) P9 promoter depends on a 557-bp sequence located within the overlapping 3' sequences for viral capsid and nonstructural genes. Utilizing a somatic transformation assay to assess JcDNV promoter activity in Drosophila melanogaster and Plodia interpunctella, viral sequences were subjected to deletional analysis. Removal of a 685-bp fragment reduced P9-driven expression to background levels. Inclusion of a second expression cassette demonstrated vector persistence and confirmed somatic transformation. P9 promoter-driven expression was restored by insertion of a 557-bp JcDNV fragment or by inclusion of a heterologous baculovirus hr5 enhancer. Consensus polycomb transcriptional factor binding sites were identified within the 557-bp fragment, which suggests a potential role in regulating densoviral transcription.
孔雀蛱蝶浓核病毒(JcDNV)P9启动子的转录活性取决于位于病毒衣壳和非结构基因重叠3'序列内的一段557 bp的序列。利用体细胞转化试验评估JcDNV启动子在黑腹果蝇和印度谷螟中的活性,对病毒序列进行缺失分析。去除一段685 bp的片段可将P9驱动的表达降低至背景水平。包含第二个表达盒证明了载体的持久性并确认了体细胞转化。通过插入一段557 bp的JcDNV片段或包含一个异源杆状病毒hr5增强子可恢复P9启动子驱动的表达。在这段557 bp的片段中鉴定出了共有的多梳转录因子结合位点,这表明其在调节浓核病毒转录中可能发挥作用。