Emanoil-Ravier R, Mercier G, Canivet M, Garcette M, Lasneret J, Peronnet F, Best-Belpomme M, Peries J
Laboratoire de Virologie des Leucémies, LOI Centre National de la Recherche Scientifique, Hôpital Saint-Louis, Paris, France.
J Virol. 1988 Oct;62(10):3867-9. doi: 10.1128/JVI.62.10.3867-3869.1988.
Dexamethasone treatment enhances expression of transposable intracisternal type A particles (IAP) at RNA and proteins levels in a murine retrovirus-transformed cell line (Ki-BALB). This effect was ascertained by electron microscopic numeration of IAP. By sequence comparison, we located glucocorticoid-responsive elements in IAP long terminal repeats. Their regulatory potential was tested on the promoter activity of an IAP long terminal repeat construct coupled with the chloramphenicol acetyltransferase gene. Our findings suggest that the IAP activation by dexamethasone occurs at the level of transcription.
地塞米松治疗可增强小鼠逆转录病毒转化细胞系(Ki-BALB)中A型顺式内粒状转座子(IAP)在RNA和蛋白质水平的表达。通过IAP的电子显微镜计数确定了这种效应。通过序列比较,我们在IAP长末端重复序列中定位了糖皮质激素反应元件。在与氯霉素乙酰转移酶基因偶联的IAP长末端重复序列构建体的启动子活性上测试了它们的调控潜力。我们的研究结果表明,地塞米松对IAP的激活发生在转录水平。