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Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters.Ume6介导的基因沉默作用涉及到一个包含Sin3共抑制因子和Rpd3组蛋白去乙酰化酶的复合物被招募到目标启动子上。
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RAD9 and DNA polymerase epsilon form parallel sensory branches for transducing the DNA damage checkpoint signal in Saccharomyces cerevisiae.RAD9和DNA聚合酶ε在酿酒酵母中形成平行的传感分支,用于转导DNA损伤检查点信号。
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Structural studies of p21Waf1/Cip1/Sdi1 in the free and Cdk2-bound state: conformational disorder mediates binding diversity.游离态及与Cdk2结合态的p21Waf1/Cip1/Sdi1的结构研究:构象无序介导结合多样性
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Conjugation, meiosis, and the osmotic stress response are regulated by Spc1 kinase through Atf1 transcription factor in fission yeast.在裂殖酵母中,结合作用、减数分裂和渗透应激反应由Spc1激酶通过Atf1转录因子进行调控。
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Distinct roles of yeast MEC and RAD checkpoint genes in transcriptional induction after DNA damage and implications for function.酵母MEC和RAD检查点基因在DNA损伤后转录诱导中的不同作用及其功能意义
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A simple and efficient method for the isolation of total RNA from the fission yeast Schizosaccharomyces pombe.一种从裂殖酵母粟酒裂殖酵母中分离总RNA的简单高效方法。
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Msn2p, a zinc finger DNA-binding protein, is the transcriptional activator of the multistress response in Saccharomyces cerevisiae.Msn2p是一种锌指DNA结合蛋白,是酿酒酵母中多重应激反应的转录激活因子。
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10
The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STRE).酿酒酵母锌指蛋白Msn2p和Msn4p是通过应激反应元件(STRE)进行转录诱导所必需的。
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UME6在酿酒酵母中对一个DNA修复基因转录调控中的作用。

Role of UME6 in transcriptional regulation of a DNA repair gene in Saccharomyces cerevisiae.

作者信息

Sweet D H, Jang Y K, Sancar G B

机构信息

Department of Biochemistry and Biophysics, School of Medicine, The University of North Carolina at Chapel Hill, 27599-7260, USA.

出版信息

Mol Cell Biol. 1997 Nov;17(11):6223-35. doi: 10.1128/MCB.17.11.6223.

DOI:10.1128/MCB.17.11.6223
PMID:9343383
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC232473/
Abstract

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.

摘要

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。