Herault Y, Chatelain G, Brun G, Michel D
Laboratoire de Biologie Moléculaire et Cellulaire, UMR49 CNRS/Ecole Normale Supérieure de Lyon, France.
Nucleic Acids Res. 1992 Dec 11;20(23):6377-83. doi: 10.1093/nar/20.23.6377.
We have isolated the avian gene T64 corresponding to the mammalian clusterin, on the basis of high accumulation of its template mRNA in cells infected with oncogenic retroviruses. Since the clusterin was shown to have a protective effect against the immune system, its induction by oncogenic viruses is of major biological importance. The unique, short 5 kb-long T64 genomic locus is inactive in normal quail embryo fibroblasts in primary culture whereas it shows a high transcriptional activity after transformation by the Rous sarcoma virus. The 963 bp-long 5' flanking region is sufficient to drive the transcription of the chloramphenicol acetyltransferase reporter gene in a thermodependent manner when a thermosensitive version of pp60v-src is used. Deletion and point mutation analyses of the promoter show that the v-src response requires at least two separate elements: PUR and AP-1, located respectively at positions -167 to -152 and -25 to -19 relative to the single transcription initiation site. In addition, the binding of specific nuclear factors to these responsive elements correlates with the T64 promoter activation.
我们基于致癌逆转录病毒感染的细胞中其模板mRNA的高积累,分离出了与哺乳动物簇集蛋白相对应的禽类基因T64。由于簇集蛋白已被证明对免疫系统具有保护作用,致癌病毒对其诱导具有重要的生物学意义。独特的、短的5kb长的T64基因组位点在原代培养的正常鹌鹑胚胎成纤维细胞中无活性,而在劳斯肉瘤病毒转化后显示出高转录活性。当使用pp60v-src的热敏版本时,963bp长的5'侧翼区域足以以热依赖的方式驱动氯霉素乙酰转移酶报告基因的转录。启动子的缺失和点突变分析表明,v-src反应至少需要两个独立的元件:PUR和AP-1,分别位于相对于单一转录起始位点的-167至-152和-25至-19位置。此外,特定核因子与这些反应元件的结合与T64启动子激活相关。