Yang R, Wek S A, Wek R C
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Mol Cell Biol. 2000 Apr;20(8):2706-17. doi: 10.1128/MCB.20.8.2706-2717.2000.
Phosphorylation of the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) is a well-characterized mechanism regulating protein synthesis in response to environmental stresses. In the yeast Saccharomyces cerevisiae, starvation for amino acids induces phosphorylation of eIF-2alpha by Gcn2 protein kinase, leading to elevated translation of GCN4, a transcriptional activator of more than 50 genes. Uncharged tRNA that accumulates during amino acid limitation is proposed to activate Gcn2p by associating with Gcn2p sequences homologous to histidyl-tRNA synthetase (HisRS) enzymes. Given that eIF-2alpha phosphorylation in mammals is induced in response to both carbohydrate and amino acid limitations, we addressed whether activation of Gcn2p in yeast is also controlled by different nutrient deprivations. We found that starvation for glucose induces Gcn2p phosphorylation of eIF-2alpha and stimulates GCN4 translation. Induction of eIF-2alpha phosphorylation by Gcn2p during glucose limitation requires the function of the HisRS-related domain but is largely independent of the ribosome binding sequences of Gcn2p. Furthermore, Gcn20p, a factor required for Gcn2 protein kinase stimulation of GCN4 expression in response to amino acid starvation, is not essential for GCN4 translational control in response to limitation for carbohydrates. These results indicate there are differences between the mechanisms regulating Gcn2p activity in response to amino acid and carbohydrate deficiency. Gcn2p induction of GCN4 translation during carbohydrate limitation enhances storage of amino acids in the vacuoles and facilitates entry into exponential growth during a shift from low-glucose to high-glucose medium. Gcn2p function also contributes to maintenance of glycogen levels during prolonged glucose starvation, suggesting a linkage between amino acid control and glycogen metabolism.
真核起始因子2(eIF - 2α)的α亚基磷酸化是一种已被充分表征的机制,可响应环境应激调节蛋白质合成。在酿酒酵母中,氨基酸饥饿会诱导Gcn2蛋白激酶使eIF - 2α磷酸化,导致GCN4(一种超过50个基因的转录激活因子)的翻译增加。有人提出,在氨基酸限制期间积累的未负载tRNA通过与Gcn2p中与组氨酰 - tRNA合成酶(HisRS)酶同源的序列结合来激活Gcn2p。鉴于哺乳动物中eIF - 2α磷酸化是对碳水化合物和氨基酸限制的共同响应,我们研究了酵母中Gcn2p的激活是否也受不同营养剥夺的控制。我们发现葡萄糖饥饿会诱导Gcn2p使eIF - 2α磷酸化并刺激GCN4翻译。在葡萄糖限制期间,Gcn2p诱导的eIF - 2α磷酸化需要HisRS相关结构域的功能,但在很大程度上独立于Gcn2p的核糖体结合序列。此外,Gcn20p是Gcn2蛋白激酶在响应氨基酸饥饿时刺激GCN4表达所必需的因子,但在响应碳水化合物限制时对GCN4的翻译控制并非必需。这些结果表明,在响应氨基酸和碳水化合物缺乏时调节Gcn2p活性的机制存在差异。在碳水化合物限制期间,Gcn2p诱导GCN4翻译可增强氨基酸在液泡中的储存,并促进从低葡萄糖培养基转变为高葡萄糖培养基时进入指数生长期。Gcn2p功能在长时间葡萄糖饥饿期间也有助于维持糖原水平,这表明氨基酸控制与糖原代谢之间存在联系。