首页> 美国卫生研究院文献>Molecular and Cellular Biology >Novel Gal3 proteins showing altered Gal80p binding cause constitutive transcription of Gal4p-activated genes in Saccharomyces cerevisiae.
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Novel Gal3 proteins showing altered Gal80p binding cause constitutive transcription of Gal4p-activated genes in Saccharomyces cerevisiae.

机译:显示改变的Gal80p结合的新型Gal3蛋白导致啤酒酵母中Gal4p激活基因的组成型转录。

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摘要

Gal4p-mediated activation of galactose gene expression in Saccharomyces cerevisiae normally requires both galactose and the activity of Gal3p. Recent evidence suggests that in cells exposed to galactose, Gal3p binds to and inhibits Ga180p, an inhibitor of the transcriptional activator Gal4p. Here, we report on the isolation and characterization of novel mutant forms of Gal3p that can induce Gal4p activity independently of galactose. Five mutant GAL3(c) alleles were isolated by using a selection demanding constitutive expression of a GAL1 promoter-driven HIS3 gene. This constitutive effect is not due to overproduction of Gal3p. The level of constitutive GAL gene expression in cells bearing different GAL3(c) alleles varies over more than a fourfold range and increases in response to galactose. Utilizing glutathione S-transferase-Gal3p fusions, we determined that the mutant Gal3p proteins show altered Gal80p-binding characteristics. The Gal3p mutant proteins differ in their requirements for galactose and ATP for their Gal80p-binding ability. The behavior of the novel Gal3p proteins provides strong support for a model wherein galactose causes an alteration in Gal3p that increases either its ability to bind to Gal80p or its access to Gal80p. With the Gal3p-Gal80p interaction being a critical step in the induction process, the Gal3p proteins constitute an important new reagent for studying the induction mechanism through both in vivo and in vitro methods.
机译:Gal4p介导的酿酒酵母中半乳糖基因表达的激活通常需要半乳糖和Gal3p的活性。最近的证据表明,在暴露于半乳糖的细胞中,Gal3p结合并抑制Ga180p(转录激活因子Gal4p的抑制剂)。在这里,我们报告的Gal3p的新型突变形式的分离和表征,可以独立于半乳糖诱导Gal4p活性。通过使用要求GAL1启动子驱动的HIS3基因组成型表达的选择,分离了五个突变GAL3(c)等位基因。这种本构作用不是由于Gal3p的过量产生。携带不同GAL3(c)等位基因的细胞中组成型GAL基因表达水平的变化范围超过四倍,并且对半乳糖的反应有所增加。利用谷胱甘肽S-转移酶-Gal3p融合,我们确定突变的Gal3p蛋白表现出改变的Gal80p结合特征。 Gal3p突变蛋白​​对半乳糖和ATP的Gal80p结合能力的要求不同。新型Gal3p蛋白的行为为模型提供了强有力的支持,其中半乳糖引起Gal3p的改变,从而增加了其与Gal80p结合的能力或与Gal80p的结合。 Gal3p-Gal80p相互作用是诱导过程中的关键步骤,Gal3p蛋白构成了重要的新试剂,可通过体内和体外方法研究诱导机制。

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