Pani L, Quian X B, Clevidence D, Costa R H
Department of Biochemistry, University of Illinois College of Medicine, Chicago 60612.
Mol Cell Biol. 1992 Feb;12(2):552-62. doi: 10.1128/mcb.12.2.552-562.1992.
The transcription factor hepatocyte nuclear factor 3 (HNF-3) is involved in the coordinate expression of several liver genes. HNF-3 DNA binding activity is composed of three different liver proteins which recognize the same DNA site. The HNF-3 proteins (designated alpha, beta, and gamma) possess homology in the DNA binding domain and in several additional regions. To understand the cell-type-specific expression of HNF-3 beta, we have defined the regulatory sequences that elicit hepatoma-specific expression. Promoter activity requires -134 bp of HNF-3 beta proximal sequences and binds four nuclear proteins, including two ubiquitous factors. One of these promoter sites interacts with a novel cell-specific factor, LF-H3 beta, whose binding activity correlates with the HNF-3 beta tissue expression pattern. Furthermore, there is a binding site for the HNF-3 protein within its own promoter, suggesting that an autoactivation mechanism is involved in the establishment of HNF-3 beta expression. We propose that both the LF-H3 beta and HNF-3 sites play an important role in the cell-type-specific expression of the HNF-3 beta transcription factor.
转录因子肝细胞核因子3(HNF-3)参与多种肝脏基因的协同表达。HNF-3的DNA结合活性由三种不同的肝脏蛋白组成,它们识别相同的DNA位点。HNF-3蛋白(分别命名为α、β和γ)在DNA结合结构域和其他几个区域具有同源性。为了了解HNF-3β的细胞类型特异性表达,我们确定了引发肝癌特异性表达的调控序列。启动子活性需要HNF-3β近端序列的-134bp,并结合四种核蛋白,包括两种普遍存在的因子。其中一个启动子位点与一种新的细胞特异性因子LF-H3β相互作用,其结合活性与HNF-3β的组织表达模式相关。此外,在其自身启动子内存在一个HNF-3蛋白的结合位点,这表明自激活机制参与了HNF-3β表达的建立。我们认为LF-H3β和HNF-3位点在HNF-3β转录因子的细胞类型特异性表达中都起着重要作用。