Valhmu W B, Palmer G D, Dobson J, Fischer S G, Ratcliffe A
Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Columbia University, New York, New York 10032, USA.
J Biol Chem. 1998 Mar 13;273(11):6196-202. doi: 10.1074/jbc.273.11.6196.
Identification and characterization of the regulatory elements of the human aggrecan gene are necessary first steps in addressing the molecular mechanisms through which the gene is regulated. Using luciferase reporter constructs driven by the human aggrecan promoter or the cytomegalovirus promoter, the 5'- and 3'-untranslated regions of the human aggrecan gene were found to regulate gene expression transcriptionally in a promoter- and/or cell type-specific manner. Independent of cell type, the 5'-untranslated region was inhibitory with respect to the cytomegalovirus promoter, but it was stimulatory to the human aggrecan promoter. The 5'-untranslated region inhibited the cytomegalovirus promoter by approximately 60% in both chondrocytes and NIH 3T3 cells, but it stimulated the activity of the human aggrecan promoter about 8-fold in chondrocytes and 40-fold in NIH 3T3 cells. In contrast, the 3'-untranslated region inhibited the activities of the human aggrecan promoter by 40-70% in both cell types, but it stimulated the cytomegalovirus promoter activities by 50-60% in NIH 3T3 cells and inhibited its activity by 70% in chondrocytes. The differential effects of the untranslated regions on the two types of promoters may be a reflection of differences in regulation of TATA-less promoters, such as the human aggrecan promoter, and TATA-containing promoters, such as the cytomegalovirus promoter.
鉴定和表征人类聚集蛋白聚糖基因的调控元件是探究该基因调控分子机制的必要第一步。利用由人类聚集蛋白聚糖启动子或巨细胞病毒启动子驱动的荧光素酶报告构建体,发现人类聚集蛋白聚糖基因的5'和3'非翻译区以启动子和/或细胞类型特异性方式转录调控基因表达。与细胞类型无关,5'非翻译区对巨细胞病毒启动子具有抑制作用,但对人类聚集蛋白聚糖启动子具有刺激作用。在软骨细胞和NIH 3T3细胞中,5'非翻译区均使巨细胞病毒启动子活性降低约60%,但在软骨细胞中使人类聚集蛋白聚糖启动子活性增强约8倍,在NIH 3T3细胞中增强约40倍。相比之下,3'非翻译区在两种细胞类型中均使人类聚集蛋白聚糖启动子活性降低40%-70%,但在NIH 3T3细胞中使巨细胞病毒启动子活性增强50%-60%,在软骨细胞中使其活性降低70%。非翻译区对两种类型启动子的不同影响可能反映了无TATA启动子(如人类聚集蛋白聚糖启动子)和含TATA启动子(如巨细胞病毒启动子)在调控上的差异。