Ding Jiabo, Cui Zhizhong, Lee Lucy F
Animal Science and Technology College, Shandong Agricultural University, Taian, Shandong 271018, China.
Virus Genes. 2007 Dec;35(3):643-50. doi: 10.1007/s11262-007-0129-5. Epub 2007 Jul 6.
The pp38 and pp24 genes of Marek's diseases virus (MDV) share the same promoter, which controls the transcription of pp38 or pp24 and a 1.8-kb mRNA bi-directionally. To understand the trans-activating activity of pp38 and pp24 on the bi-directional promoter, both genes were cloned into pcDNA-3 or pBudCE4.1 vectors either singly or in combination. These plasmids were expressed in transfected chicken embryonic fibroblast (CEF) cells. Chloramphenicol acetyltransferase (CAT) activity expressed under the control of the promoter in CEF co-transfected with pP(1.8 kb)-CAT and pBud-pp38-pp24 was significantly higher than that following transfection with only pBud-pp38 or pBud-pp24. This indicates the combination of pp24 and pp38 together are essential for the activation of the promoter. In DNA mobility shift assays, the promoter binds to pp38 and pp24 together, but not to pp38 or pp24 alone. By competitive inhibition tests with a set of DNA fragments from the promoter region, the sequence 5'-CTGCTCATTT-3' was identified as the core sequence for binding by pp38-pp24 in up-regulation of the bi-directional promoter activity.
马立克氏病病毒(MDV)的pp38和pp24基因共享同一个启动子,该启动子双向控制pp38或pp24以及一个1.8 kb mRNA的转录。为了解pp38和pp24对双向启动子的反式激活活性,将这两个基因单独或组合克隆到pcDNA-3或pBudCE4.1载体中。这些质粒在转染的鸡胚成纤维细胞(CEF)中表达。在与pP(1.8 kb)-CAT和pBud-pp38-pp24共转染的CEF中,在启动子控制下表达的氯霉素乙酰转移酶(CAT)活性显著高于仅转染pBud-pp38或pBud-pp24后的活性。这表明pp24和pp38组合在一起对于启动子的激活至关重要。在DNA迁移率变动分析中,启动子与pp38和pp24一起结合,但不与单独的pp38或pp24结合。通过用一组来自启动子区域的DNA片段进行竞争性抑制试验,序列5'-CTGCTCATTT-3'被确定为在双向启动子活性上调中pp38-pp24结合的核心序列。