Erickson F L, Hannig E M
University of Texas at Dallas, Department of Molecular and Cell Biology, Richardson 75083-0688, USA.
EMBO J. 1996 Nov 15;15(22):6311-20.
Eukaryotic translation initiation factor 2 (eIF-2) comprises three non-identical subunits alpha, beta and gamma. In vitro, eIF-2 binds the initiator methionyl-tRNA in a GTP-dependent fashion. Based on similarities between eukaryotic eIF-2gamma proteins and eubacterial EF-Tu proteins, we previously proposed a major role for the gamma-subunit in binding guanine nucleotide and tRNA. We have tested this hypothesis by examining the biochemical activities of yeast eIF-2 purified from wild-type strains and strains harboring mutations in the eIF-2gamma structural gene (GCD11) predicted to alter ligand binding by eIF-2. The alteration of tyrosine 142 in yeast eIF-2gamma, corresponding to histidine 66 in Escherichia coli EF-Tu, dramatically reduced the affinity of eIF-2 for Met-tRNAi(Met) without affecting the k(off) value for guanine nucleotides. In contrast, non-lethal substitutions at a conserved lysine residue (K250) in the putative guanine ring-binding loop increased the off-rate for GDP, thereby mimicking the function of the guanine nucleotide exchange factor eIF-2B, without altering the apparent dissociation constant for Met-tRNAi(Met). For eIF-2[gamma-K250R], the increased off-rate also seen for GTP was masked by the presence of Met-tRNAi(Met) in vitro. In vivo, increasing the dose of the yeast initiator tRNA gene suppressed the slow-growth phenotype and reduced GCN4 expression in gcd11-K250R and gcd11-Y142H strains. These studies indicate that the gamma-subunit of eIF-2 does indeed provide EF-Tu-like function to the eIF-2 complex, and further suggest that the level of Met-tRNAi(Met) is critical for maintaining wild-type rates of initiation in vivo.
真核生物翻译起始因子2(eIF-2)由三个不同的亚基α、β和γ组成。在体外,eIF-2以GTP依赖的方式结合起始甲硫氨酰-tRNA。基于真核生物eIF-2γ蛋白与原核生物EF-Tu蛋白之间的相似性,我们之前提出γ亚基在结合鸟嘌呤核苷酸和tRNA方面起主要作用。我们通过检测从野生型菌株和在eIF-2γ结构基因(GCD11)中携带预测会改变eIF-2配体结合的突变的菌株中纯化的酵母eIF-2的生化活性来验证这一假设。酵母eIF-2γ中酪氨酸142的改变,对应于大肠杆菌EF-Tu中的组氨酸66,显著降低了eIF-2对Met-tRNAi(Met)的亲和力,而不影响鸟嘌呤核苷酸的解离速率常数(k(off)值)。相反,在假定的鸟嘌呤环结合环中保守赖氨酸残基(K250)处的非致死性取代增加了GDP的解离速率,从而模拟了鸟嘌呤核苷酸交换因子eIF-2B的功能,而不改变Met-tRNAi(Met)的表观解离常数。对于eIF-2[γ-K250R],在体外Met-tRNAi(Met)的存在掩盖了GTP解离速率增加的现象。在体内,增加酵母起始tRNA基因的剂量可抑制gcd11-K250R和gcd11-Y142H菌株的生长缓慢表型并降低GCN4表达。这些研究表明,eIF-2的γ亚基确实为eIF-2复合物提供了类似EF-Tu的功能,并进一步表明Met-tRNAi(Met)的水平对于维持体内野生型起始速率至关重要。