Ni H T, LaPorte D C
Department of Biochemistry, University of Minnesota, Minneapolis 55455, USA.
Mol Microbiol. 1995 Jun;16(6):1197-205. doi: 10.1111/j.1365-2958.1995.tb02342.x.
In the yeast Saccharomyces cerevisiae, glycogen synthase is encoded by two genes: GSY1 and GSY2. The activity of the enzymes increases as cultures enter the stationary phase of growth. Using a GSY2::lacZ fusion gene, we have demonstrated that the increase in glycogen synthase activity resulted, at least in part, from an increase in the level of the protein rather than simply from a change in its phosphorylation state. Northern blot analysis showed a parallel increase in the level of the GSY2 mRNA, which is consistent with transcriptional activation of GSY2. Deletion analysis identified three regions upstream of GSY2 which are involved in GSY2 expression: regions A (-390 to -347 relative to the start of translation), B (-252 to -209) and C (-209 to -167). Region A or C independently activated expression of GSY2. In contrast, region B alone yielded only modest expression. Expression of GSY2 is induced by growth to stationary phase, heat shock or nitrogen starvation. Response to these stressors is mediated by elements within regions A and C. These elements appear to be related to the stress-response elements found in other stress-responsive genes.
在酿酒酵母中,糖原合酶由两个基因编码:GSY1和GSY2。随着培养物进入生长稳定期,这些酶的活性增加。利用一个GSY2::lacZ融合基因,我们已经证明糖原合酶活性的增加至少部分是由于蛋白质水平的提高,而不仅仅是其磷酸化状态的改变。Northern印迹分析显示GSY2 mRNA水平平行增加,这与GSY2的转录激活一致。缺失分析确定了GSY2上游参与GSY2表达的三个区域:区域A(相对于翻译起始位点为-390至-347)、区域B(-252至-209)和区域C(-209至-167)。区域A或C可独立激活GSY2的表达。相比之下,单独的区域B仅产生适度的表达。GSY2的表达由生长至稳定期、热休克或氮饥饿诱导。对这些应激源的反应由区域A和C内的元件介导。这些元件似乎与其他应激反应基因中发现的应激反应元件有关。