Ho I C, Leiden J M
Howard Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor 48109.
J Exp Med. 1990 Nov 1;172(5):1443-9. doi: 10.1084/jem.172.5.1443.
T cell-specific expression of the human T cell receptor alpha (TCR-alpha) gene is regulated by the interaction of variable region promoter elements with a transcriptional enhancer that is located 4.5 kb 3' of the TCR-alpha constant region (C alpha) gene segment. The minimal TCR-alpha enhancer is composed of two nuclear protein binding sites, T alpha 1 and T alpha 2, that are both required for the T cell-specific activity of the enhancer. The T alpha 1 binding site contains a consensus cAMP response element (CRE), and binds a set of ubiquitous nuclear proteins. The T alpha 2 binding site does not contain known transcriptional enhancer motifs. However, it binds at least two nuclear protein complexes, one of which is T cell specific. We now report that although the T alpha 2 nuclear protein binding site displays transcriptional activator activity in the context of the TCR-alpha enhancer, this site alone can function as a potent, T cell-specific transcriptional repressor when positioned either upstream, or downstream of several heterologous promoter and enhancer elements. These results demonstrate that a single nuclear protein binding site can function as a T cell-specific transcriptional activator or repressor element, depending upon the context in which it is located.
人类T细胞受体α(TCR-α)基因的T细胞特异性表达受可变区启动子元件与转录增强子相互作用的调控,该增强子位于TCR-α恒定区(Cα)基因片段下游4.5 kb处。最小的TCR-α增强子由两个核蛋白结合位点Tα1和Tα2组成,这两个位点都是增强子T细胞特异性活性所必需的。Tα1结合位点包含一个共有cAMP反应元件(CRE),并结合一组普遍存在的核蛋白。Tα2结合位点不包含已知的转录增强子基序。然而,它结合至少两种核蛋白复合物,其中一种是T细胞特异性的。我们现在报告,虽然Tα2核蛋白结合位点在TCR-α增强子的背景下显示出转录激活活性,但当位于几个异源启动子和增强子元件的上游或下游时,该位点本身可作为一种有效的T细胞特异性转录抑制因子发挥作用。这些结果表明,单个核蛋白结合位点可作为T细胞特异性转录激活因子或抑制因子元件发挥作用,这取决于它所处的背景。