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Nrg1 Is a Transcriptional Repressor for Glucose Repression of STA1 Gene Expression in Saccharomyces cerevisiae

机译:Nrg1是酿酒酵母中STA1基因表达的葡萄糖阻遏转录抑制子。

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摘要

Expression of genes encoding starch-degrading enzymes is regulated by glucose repression in the yeast Saccharomyces cerevisiae. We have identified a transcriptional repressor, Nrg1, in a genetic screen designed to reveal negative factors involved in the expression of STA1, which encodes a glucoamylase. The NRG1 gene encodes a 25-kDa C2H2 zinc finger protein which specifically binds to two regions in the upstream activation sequence of the STA1 gene, as judged by gel retardation and DNase I footprinting analyses. Disruption of the NRG1 gene causes a fivefold increase in the level of the STA1 transcript in the presence of glucose. The expression of NRG1 itself is inhibited in the absence of glucose. DNA-bound LexA-Nrg1 represses transcription of a target gene 10.7-fold in a glucose-dependent manner, and this repression is abolished in both ssn6 and tup1 mutants. Two-hybrid and glutathione S-transferase pull-down experiments show an interaction of Nrg1 with Ssn6 both in vivo and in vitro. These findings indicate that Nrg1 acts as a DNA-binding repressor and mediates glucose repression of the STA1 gene expression by recruiting the Ssn6-Tup1 complex.
机译:编码糖降解酶的基因的表达受酿酒酵母中葡萄糖抑制的调节。我们已经确定了一种基因筛选中的转录阻遏物Nrg1,以揭示与STA1编码葡糖淀粉酶的表达有关的负面因素。 NRG1基因编码一个25 kDa C2H2锌指蛋白,可通过凝胶阻滞和DNase I足迹分析判断,该蛋白与STA1基因上游激活序列中的两个区域特异性结合。在存在葡萄糖的情况下,NRG1基因的破坏导致STA1转录水平增加了五倍。在不存在葡萄糖的情况下,NRG1本身的表达受到抑制。 DNA结合的LexA-Nrg1以葡萄糖依赖性方式抑制靶基因的转录10.7倍,并且在ssn6和tup1突变体中都取消了这种抑制。两种杂合和谷胱甘肽S-转移酶下拉实验均显示Nrg1与Ssn6在体内和体外都有相互作用。这些发现表明,Nrg1充当DNA结合阻遏物,并通过募集Ssn6-Tup1复合体来介导STA1基因表达的葡萄糖抑制。

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