Yang W, Hinnebusch A G
Laboratory of Eukaryotic Gene Regulation, National Institute of Child Health and Human Development, Bethesda, Maryland 20892-2785, USA.
Mol Cell Biol. 1996 Nov;16(11):6603-16. doi: 10.1128/MCB.16.11.6603.
Eukaryotic translation initiation factor 2B (eIF2B) is a five-subunit complex that catalyzes guanine nucleotide exchange on eIF2. Phosphorylation of the alpha subunit of eIF2 [creating eIF2(alphaP]) converts eIF2 x GDP from a substrate to an inhibitor of eIF2B. We showed previously that the inhibitory effect of eIF2(alphaP) can be decreased by deletion of the eIF2B alpha subunit (encoded by GCN3) and by point mutations in the beta and delta subunits of eIF2B (encoded by GCD7 and GCD2, respectively). These findings, plus sequence similarities among GCD2, GCD7, and GCN3, led us to propose that these proteins comprise a regulatory domain that interacts with eIF2(alphaP) and mediates the inhibition of eIF2B activity. Supporting this hypothesis, we report here that overexpression of GCD2, GCD7, and GCN3 specifically reduced the inhibitory effect of eIF2(alphaP) on translation initiation in vivo. The excess GCD2, GCD7, and GCN3 were coimmunoprecipitated from cell extracts, providing physical evidence that these three proteins can form a stable subcomplex. Formation of this subcomplex did not compensate for a loss of eIF2B function by mutation and in fact lowered eIF2B activity in strains lacking eIF2(alphaP). These findings indicate that the trimeric subcomplex does not possess guanine nucleotide exchange activity; we propose, instead, that it interacts with eIF2(alphaP) and prevents the latter from inhibiting native eIF2B. Overexpressing only GCD2 and GCD7 also reduced eIF2(alphaP) toxicity, presumably by titrating GCN3 from eIF2B and producing the four-subunit form of eIF2B that is less sensitive to eIF2(alphaP). This interpretation is supported by the fact that overexpressing GCD2 and GCD7 did not reduce eIF2(alphaP) toxicity in a strain lacking GCN3; however, it did suppress the impairment of eIF2B caused by the gcn3c-R104K mutation. An N-terminally truncated GCD2 protein interacted with other eIF2B subunits only when GCD7 and GCN3 were overexpressed, in accordance with the idea that the portion of GCD2 homologous to GCD7 and GCN3 is sufficient for complex formation by these three proteins. Together, our results provide strong evidence that GCN3, GCD7, and the C-terminal half of GCD2 comprise the regulatory domain in eIF2B.
真核生物翻译起始因子2B(eIF2B)是一种由五个亚基组成的复合物,可催化eIF2上的鸟嘌呤核苷酸交换。eIF2α亚基的磷酸化(产生eIF2(αP))将eIF2·GDP从底物转变为eIF2B的抑制剂。我们之前表明,通过缺失eIF2Bα亚基(由GCN3编码)以及eIF2Bβ和δ亚基(分别由GCD7和GCD2编码)中的点突变,可以降低eIF2(αP)的抑制作用。这些发现,加上GCD2、GCD7和GCN3之间的序列相似性,使我们提出这些蛋白质组成一个调节结构域,该结构域与eIF2(αP)相互作用并介导对eIF2B活性的抑制。支持这一假设的是,我们在此报告,GCD2、GCD7和GCN3的过表达特异性降低了eIF2(αP)在体内对翻译起始的抑制作用。过量的GCD2、GCD7和GCN3从细胞提取物中被共免疫沉淀,提供了这三种蛋白质可以形成稳定亚复合物的物理证据。这种亚复合物的形成并不能通过突变来补偿eIF2B功能的丧失,实际上在缺乏eIF2(αP)的菌株中降低了eIF2B的活性。这些发现表明三聚体亚复合物不具有鸟嘌呤核苷酸交换活性;相反,我们提出它与eIF2(αP)相互作用并阻止后者抑制天然eIF2B。仅过表达GCD2和GCD7也降低了eIF2(αP)的毒性,推测是通过从eIF2B中滴定GCN3并产生对eIF2(αP)不太敏感的四亚基形式的eIF2B。这一解释得到以下事实的支持:在缺乏GCN3的菌株中过表达GCD2和GCD7并没有降低eIF2(αP)的毒性;然而,它确实抑制了由gcn3c - R104K突变引起的eIF2B损伤。N端截短的GCD2蛋白仅在GCD7和GCN3过表达时才与其他eIF2B亚基相互作用,这与GCD2中与GCD7和GCN3同源的部分足以使这三种蛋白质形成复合物的观点一致。总之,我们的结果提供了强有力的证据,表明GCN3、GCD7和GCD2的C端一半组成了eIF2B中的调节结构域。