Ozcan S, Vallier L G, Flick J S, Carlson M, Johnston M
Department of Genetics, Washington University School of Medicine, St Louis, MO 63110, USA.
Yeast. 1997 Feb;13(2):127-37. doi: 10.1002/(SICI)1097-0061(199702)13:2<127::AID-YEA68>3.0.CO;2-#.
High levels of glucose repress expression of the SUC2 gene in the yeast Saccharomyces cerevisiae. We have discovered that low levels of glucose are required for maximal transcription of SUC2: SUC2 expression is induced about five- to ten-fold in cells growing on low levels of glucose (0.1%) compared to cells growing on galactose or glycerol. Two pieces of evidence suggest that this low-glucose-induced expression is mediated by a repression mechanism that involves an upstream repression site in the SUC2 promoter (URS(SUC2)). First, deletion of the URS(SUC2) results in expression of the SUC2 gene in the absence of glucose, and second the URS(SUC2) mediates a six-fold repression of a reporter gene when inserted into a heterologous promoter. However, this URS(SUC2) mediated repression occurs on all tested carbon sources, suggesting that this URS element acts in concert with all other promoter elements to respond to low concentrations of glucose. This repression requires the general repressor SSn6p. SNF3, which encodes a glucose transporter that appears to be a sensor of low levels of glucose, is also required for low-glucose-induced expression of SUC2.
高浓度葡萄糖会抑制酿酒酵母中SUC2基因的表达。我们发现,低浓度葡萄糖是SUC2基因实现最大转录所必需的:与在半乳糖或甘油上生长的细胞相比,在低浓度葡萄糖(0.1%)上生长的细胞中,SUC2基因的表达被诱导提高了约五到十倍。有两条证据表明,这种低葡萄糖诱导的表达是由一种抑制机制介导的,该机制涉及SUC2启动子中的一个上游抑制位点(URS(SUC2))。第一,删除URS(SUC2)会导致在没有葡萄糖的情况下SUC2基因的表达,第二,当插入到异源启动子中时,URS(SUC2)会介导对报告基因六倍的抑制。然而,这种URS(SUC2)介导的抑制在所有测试的碳源上都会发生,这表明这个URS元件与所有其他启动子元件协同作用,以响应低浓度的葡萄糖。这种抑制需要通用阻遏物SSn6p。SNF3编码一种葡萄糖转运蛋白,似乎是低水平葡萄糖的传感器,它也是低葡萄糖诱导的SUC2基因表达所必需的。