Sweet D H, Jang Y K, Sancar G B
Department of Biochemistry and Biophysics, School of Medicine, The University of North Carolina at Chapel Hill, 27599-7260, USA.
Mol Cell Biol. 1997 Nov;17(11):6223-35. doi: 10.1128/MCB.17.11.6223.
In Saccharomyces cerevisiae UV radiation and a variety of chemical DNA-damaging agents induce the transcription of specific genes, including several involved in DNA repair. One of the best characterized of these genes is PHR1, which encodes the apoenzyme for DNA photolyase. Basal-level and damage-induced expression of PHR1 require an upstream activation sequence, UAS(PHR1), which has homology with DRC elements found upstream of at least 19 other DNA repair and DNA metabolism genes in yeast. Here we report the identification of the UME6 gene of S. cerevisiae as a regulator of UAS(PHR1) activity. Multiple copies of UME6 stimulate expression from UAS(PHR1) and the intact PHR1 gene. Surprisingly, the effect of deletion of UME6 is growth phase dependent. In wild-type cells PHR1 is induced in late exponential phase, concomitant with the initiation of glycogen accumulation that precedes the diauxic shift. Deletion of UME6 abolishes this induction, decreases the steady-state concentration of photolyase molecules and PHR1 mRNA, and increases the UV sensitivity of a rad2 mutant. Despite the fact that UAS(PHR1) does not contain the URS1 sequence, which has been previously implicated in UME6-mediated transcriptional regulation, we find that Ume6p binds to UAS(PHR1) with an affinity and a specificity similar to those seen for a URS1 site. Similar binding is also seen for DRC elements from RAD2, RAD7, and RAD53, suggesting that UME6 contributes to the regulated expression of a subset of damage-responsive genes in yeast.
在酿酒酵母中,紫外线辐射和多种化学DNA损伤剂可诱导特定基因的转录,包括一些参与DNA修复的基因。其中最具特征的基因之一是PHR1,它编码DNA光解酶的脱辅基酶。PHR1的基础水平表达和损伤诱导表达需要一个上游激活序列UAS(PHR1),该序列与酵母中至少19个其他DNA修复和DNA代谢基因上游发现的DRC元件具有同源性。在这里,我们报告鉴定出酿酒酵母的UME6基因是UAS(PHR1)活性的调节因子。UME6的多个拷贝刺激UAS(PHR1)和完整PHR1基因的表达。令人惊讶的是,UME6缺失的影响取决于生长阶段。在野生型细胞中,PHR1在指数后期被诱导,与双相转变之前糖原积累的开始同时发生。UME6的缺失消除了这种诱导,降低了光解酶分子和PHR1 mRNA的稳态浓度,并增加了rad2突变体对紫外线的敏感性。尽管UAS(PHR1)不包含先前与UME6介导的转录调控有关的URS1序列,但我们发现Ume6p以与URS1位点相似的亲和力和特异性结合UAS(PHR1)。对于RAD2、RAD7和RAD53的DRC元件也观察到类似的结合,这表明UME6有助于酵母中一部分损伤反应基因的调控表达。