Brazas R M, Bhoite L T, Murphy M D, Yu Y, Chen Y, Neklason D W, Stillman D J
Department of Oncological Sciences, University of Utah Health Sciences Center, Salt Lake City 84132, USA.
J Biol Chem. 1995 Dec 8;270(49):29151-61. doi: 10.1074/jbc.270.49.29151.
SW15 encodes a zinc finger DNA binding protein required for the transcription of the Saccharomyces cerevisiae HO gene, and PHO2 encodes a homeodomain DNA binding protein. In vitro biochemical studies using purified Swi5p and Pho2p proteins have demonstrated that Swi5p and Pho2p bind cooperatively to the HO promoter. In this report we investigate the regions of the Swi5p and Pho2p proteins required for cooperative DNA binding. The analysis of each protein gives a similar result: the zinc finger or homeodomain DNA binding domains are each sufficient for in vitro DNA binding, but additional regions of each protein are required for cooperative DNA binding. In vitro and in vivo experiments were conducted with promoters with altered spacing between the Pho2p and Swi5p binding sites. Mutations that increased the distance between the two binding sites had minimal effects on either in vitro cooperative DNA binding or in vivo upstream activating sequence activity. These observations suggest that the interaction domains of Swi5p and Pho2p are flexible and can tolerate an increase in distance between the two binding sites. The mechanism of the cooperative DNA binding by Swi5p and Pho2p is discussed.
SW15编码一种酿酒酵母HO基因转录所需的锌指DNA结合蛋白,而PHO2编码一种同源结构域DNA结合蛋白。使用纯化的Swi5p和Pho2p蛋白进行的体外生化研究表明,Swi5p和Pho2p协同结合HO启动子。在本报告中,我们研究了Swi5p和Pho2p蛋白协同结合DNA所需的区域。对每种蛋白的分析得出了类似的结果:锌指或同源结构域DNA结合域各自足以进行体外DNA结合,但每种蛋白的其他区域对于协同DNA结合是必需的。我们对Pho2p和Swi5p结合位点之间间距改变的启动子进行了体外和体内实验。增加两个结合位点之间距离突变对体外协同DNA结合或体内上游激活序列活性的影响最小。这些观察结果表明,Swi5p和Pho2p的相互作用结构域具有灵活性,能够耐受两个结合位点之间距离的增加。本文还讨论了Swi5p和Pho2p协同结合DNA的机制。