Li J J, Kim R H, Sodek J
MRC Group in Periodontal Physiology, Faculty of Dentistry, University of Toronto, Ontario, Canada.
Biochem J. 1995 Aug 15;310 ( Pt 1)(Pt 1):33-40. doi: 10.1042/bj3100033.
The orientation of the TATA box is thought to direct downstream transcription of eukaryotic genes by RNA polymerase II. However, the putative TATA box in the promoter of the bone sialoprotein (BSP) gene, which codes for a tissue-specific and developmentally regulated bone matrix protein, is inverted (5'-TTTATA-3') relative to the consensus TATA box sequence (5'-TATAAA-3') and is overlapped by a vitamin D3-response element. Here we show that the inverted TATA sequence in the rat BSP gene binds to recombinant TATA-box-binding protein (TBP) with an affinity similar to that observed with the consensus TATA box, and site-directed point mutations in the inverted TATA sequence (mutating TTTATA into TCTCTA) abrogate both TBP binding and BSP promoter activity. However, when the inverted TATA sequence is changed to a canonical TATAAA, the TBP- and vitamin D3 receptor-binding properties together with the BSP promoter activity are retained. In addition, we found that the TBP is required to reconstitute in vitro transcription driven by the BSP promoter. These studies, which have revealed a naturally occurring inverted TATA box that can bind TBP and direct downstream transcription, demonstrate that the orientation of the TATA box does not determine the direction of transcription in higher eukaryotic genes. Consequently, the inverted TATA box that is conserved in the human, rat and mouse BSP gene promoters will provide an excellent in vivo model to investigate the polarity of the transcription factor IID-DNA complex and its relation to downstream transcription.
TATA 框的方向被认为可指导 RNA 聚合酶 II 对真核基因进行下游转录。然而,骨唾液酸蛋白(BSP)基因启动子中的假定 TATA 框相对于共有 TATA 框序列(5'-TATAAA-3')是反向的(5'-TTTATA-3'),并且与维生素 D3 反应元件重叠。在此我们表明,大鼠 BSP 基因中的反向 TATA 序列与重组 TATA 框结合蛋白(TBP)结合的亲和力与在共有 TATA 框中观察到的相似,并且反向 TATA 序列中的定点突变(将 TTTATA 突变为 TCTCTA)会消除 TBP 结合和 BSP 启动子活性。但是,当反向 TATA 序列变为典型的 TATAAA 时,TBP 和维生素 D3 受体结合特性以及 BSP 启动子活性得以保留。此外,我们发现 TBP 是体外重建由 BSP 启动子驱动的转录所必需的。这些研究揭示了一个天然存在的可结合 TBP 并指导下游转录的反向 TATA 框,表明 TATA 框的方向并不决定高等真核基因中的转录方向。因此,在人、大鼠和小鼠 BSP 基因启动子中保守的反向 TATA 框将为研究转录因子 IID-DNA 复合物的极性及其与下游转录的关系提供一个出色的体内模型。