Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
BMC Biochem. 2010 Aug 4;11:29. doi: 10.1186/1471-2091-11-29.
When eukaryotic cells are deprived of amino acids, uncharged tRNAs accumulate and activate the conserved GCN2 protein kinase. Activated Gcn2p up-regulates the general amino acid control pathway through phosphorylation of the translational initiation factor eIF2. In Saccharomyces cerevisiae, Gcn2p is the only kinase that phosphorylates eIF2 to regulate translation through this mechanism. We addressed changes in yeast growth and tRNA aminoacylation, or charging, during amino acid depletion in the presence and absence of GCN2. tRNA charging was measured using a microarray technique which simultaneously measures all cytosolic tRNAs. A fully prototrophic strain, and its isogenic gcn2 Delta counterpart, were used to study depletion for each of the 20 amino acids, with a focus on Trp, Arg, His and Leu, which are metabolically distinct and together provide a good overview on amino acid metabolism.
While the wild-type strain had no observable phenotype upon depletion for any amino acid, the gcn2 Delta strain showed slow growth in media devoid of only Trp or Arg. Consistent with the growth phenotypes, profiles of genome-wide tRNA charging revealed significant decrease in cognate tRNA charging only in the gcn2 Delta strain upon depletion for Trp or Arg. In contrast, there was no change in tRNA charging during His and Leu depletion in either the wild-type or gcn2 Delta strains, consistent with the null effect on growth during loss of these amino acids. We determined that the growth phenotype of Trp depletion is derived from feedback inhibition of aromatic amino acid biosynthesis. By removing Phe and Tyr from the media in addition to Trp, regular growth was restored and tRNATrp charging no longer decreased. The growth phenotype of Arg depletion is derived from unbalanced nitrogen metabolism. By supplementing ornithine upon Arg depletion, both growth and tRNAArg charging were partially restored.
Under mild stress conditions the basal activity of Gcn2p is sufficient to allow for proper adaptation to amino acid depletion. This study highlights the importance of the GCN2 eIF2 kinase pathway for maintaining metabolic homeostasis, contributing to appropriate tRNA charging and growth adaptation in response to culture conditions deficient for the central amino acids, tryptophan and arginine.
当真核细胞被剥夺氨基酸时,未被电荷化的 tRNA 会积累并激活保守的 GCN2 蛋白激酶。激活的 Gcn2p 通过磷酸化翻译起始因子 eIF2 来上调一般氨基酸控制途径。在酿酒酵母中,Gcn2p 是唯一一种通过这种机制磷酸化 eIF2 来调节翻译的激酶。我们在存在和不存在 GCN2 的情况下,研究了氨基酸耗竭过程中酵母生长和 tRNA 氨酰化(或充电)的变化。使用微阵列技术测量 tRNA 充电,该技术可同时测量所有胞质 tRNA。我们使用一个完全原养型菌株及其同基因 gcn2Δ 对应菌株,研究了 20 种氨基酸中的每一种氨基酸的耗竭情况,重点研究色氨酸、精氨酸、组氨酸和亮氨酸,因为它们在代谢上有区别,一起可以很好地概述氨基酸代谢。
虽然野生型菌株在耗尽任何氨基酸时都没有观察到表型,但 gcn2Δ 菌株在缺乏色氨酸或精氨酸的培养基中生长缓慢。与生长表型一致,全基因组 tRNA 充电谱显示,只有在耗尽色氨酸或精氨酸时,gcn2Δ 菌株的对应 tRNA 充电才会显著减少。相比之下,在野生型或 gcn2Δ 菌株耗尽组氨酸和亮氨酸时,tRNA 充电没有变化,这与在失去这些氨基酸时对生长的无影响一致。我们确定色氨酸耗尽的生长表型源自芳香族氨基酸生物合成的反馈抑制。通过从培养基中去除色氨酸之外的苯丙氨酸和酪氨酸,恢复了正常生长,并且 tRNATrp 充电不再减少。精氨酸耗尽的生长表型源自氮代谢不平衡。通过在耗尽精氨酸时补充鸟氨酸,生长和 tRNAArg 充电都得到了部分恢复。
在轻度应激条件下,Gcn2p 的基础活性足以使其适应氨基酸耗尽。本研究强调了 GCN2eIF2 激酶途径对于维持代谢平衡的重要性,有助于在中央氨基酸(色氨酸和精氨酸)缺乏的培养条件下,适当调整 tRNA 充电和生长适应。