Xin Xiantong, Lan Changgui, Lee Hee Chul, Zhang Li
Department of Environmental Health Sciences, Columbia University, Mailman School of Public Health, 60 Haven Avenue, B-106, New York, NY 10032, USA.
Department of Environmental Health Sciences, Columbia University, Mailman School of Public Health, 60 Haven Avenue, B-106, New York, NY 10032, USA.
Biochem Biophys Res Commun. 2007 Oct 12;362(1):120-125. doi: 10.1016/j.bbrc.2007.07.156. Epub 2007 Aug 8.
The yeast transcriptional regulator Hap1 promotes both transcriptional activation and repression. Previous studies have shown that Hap1 binds to the promoter of its own gene and represses its transcription. In this report, we identified the DNA site that allows Hap1-binding with high affinity. This Hap1-binding site contains only one CGG triplet and is distinct from the typical Hap1-binding upstream activation sequences (UASs) mediating transcriptional activation. Furthermore, at the HAP1 promoter, Ssa is bound to DNA with Hap1, whereas Hsp90 is not bound. Intriguingly, we found that histone deacetylases, including Rpd3, Hda1, Sin3 and Hos1, are not required for the repression of the HAP1 gene by Hap1. Rather, they are required for transcriptional activation of the HAP1 promoter, and this requirement is dependent on the HAP1 basal promoter. These results reveal a complex mechanism of transcriptional regulation at the HAP1 promoter, involving multiple DNA elements and regulatory proteins.
酵母转录调节因子Hap1既能促进转录激活,也能促进转录抑制。先前的研究表明,Hap1与其自身基因的启动子结合并抑制其转录。在本报告中,我们鉴定出了能使Hap1以高亲和力结合的DNA位点。这个Hap1结合位点仅包含一个CGG三联体,并且不同于介导转录激活的典型Hap1结合上游激活序列(UASs)。此外,在HAP1启动子处,Ssa与Hap1一起结合在DNA上,而Hsp90不结合。有趣的是,我们发现包括Rpd3、Hda1、Sin3和Hos1在内的组蛋白去乙酰化酶对于Hap1对HAP1基因的抑制不是必需的。相反,它们是HAP1启动子转录激活所必需的,并且这种需求依赖于HAP1基础启动子。这些结果揭示了HAP1启动子处复杂的转录调控机制,涉及多个DNA元件和调节蛋白。