McBride H J, Brazas R M, Yu Y, Nasmyth K, Stillman D J
Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City 84132, USA.
Mol Cell Biol. 1997 May;17(5):2669-78. doi: 10.1128/MCB.17.5.2669.
The SWI5 gene encodes a zinc finger DNA-binding protein required for the transcriptional activation of the yeast HO gene. There are two Swi5p binding sites in the HO promoter, site A at -1800 and site B at -1300. Swi5p binding at site B has been investigated in some detail, and we have shown that Swi5p binds site B in a mutually cooperative fashion with Pho2p, a homeodomain protein. In this report, we demonstrate that Swi5p and Pho2p bind cooperatively to both sites A and B but that there are differences in binding to these two promoter sites. It has been shown previously that point mutations in either Swi5p binding site only modestly reduce HO expression in a PHO2 strain. We show that these mutant promoters are completely inactive in a pho2 mutant. We have created stronger point mutations at the two Swi5p binding sites within the HO promoter, and we show that the two binding sites, separated by 500 bp, are both absolutely required for HO expression, independent of PHO2. These results create an apparent dilemma, as the strong mutations at the Swi5p binding sites show that both binding sites are required for HO expression, but the earlier binding site mutations allow Swi5p to activate HO, but only in the presence of Pho2p. To explain these results, a model is proposed in which physical interaction between Swi5p proteins bound to these two sites separated by 500 bp is required for activation of the HO promoter. Experimental evidence is presented that supports the model. In addition, through deletion analysis we have identified a region near the amino terminus of Swi5p that is required for PHO2-independent activation of HO, suggesting that this region mediates the long-range interactions between Swi5p molecules bound at the distant sites.
SWI5基因编码一种锌指DNA结合蛋白,它是酵母HO基因转录激活所必需的。HO启动子中有两个Swi5p结合位点,A位点在-1800处,B位点在-1300处。对Swi5p在B位点的结合情况已进行了较为详细的研究,我们发现Swi5p与同源结构域蛋白Pho2p以相互协同的方式结合在B位点。在本报告中,我们证明Swi5p和Pho2p协同结合在A和B两个位点,但在与这两个启动子位点的结合上存在差异。先前已表明,仅Swi5p结合位点中的点突变只会适度降低PHO2菌株中HO的表达。我们发现这些突变启动子在pho2突变体中完全无活性。我们在HO启动子内的两个Swi5p结合位点处创建了更强的点突变,并且我们发现被500 bp隔开的这两个结合位点对于HO的表达都是绝对必需的,且不依赖于PHO2。这些结果造成了一个明显的困境,因为Swi5p结合位点处的强突变表明两个结合位点对于HO的表达都是必需的,但早期的结合位点突变允许Swi5p激活HO,但仅在Pho2p存在的情况下。为了解释这些结果,我们提出了一个模型,其中结合在被500 bp隔开这两个位点上的Swi5p蛋白之间的物理相互作用是激活HO启动子所必需的。文中给出了支持该模型的实验证据。此外,通过缺失分析我们确定了Swi5p氨基末端附近的一个区域,该区域是HO不依赖PHO2激活所必需的,这表明该区域介导了结合在远处位点的Swi5p分子之间的长程相互作用。