Department of Chemistry and Biochemistry and the Institute for Cellular and Molecular Biology, University of Texas, Austin, Texas 78712.
Department of Chemistry and Biochemistry and the Institute for Cellular and Molecular Biology, University of Texas, Austin, Texas 78712.
J Biol Chem. 2011 Dec 9;286(49):42566-42574. doi: 10.1074/jbc.M111.280099. Epub 2011 Sep 30.
The initiation of translation in eukaryotes requires a suite of eIFs that include the cap-binding complex, eIF4F. eIF4F is comprised of the subunits eIF4G and eIF4E and often the helicase, eIF4A. The eIF4G subunit serves as an assembly point for other initiation factors, whereas eIF4E binds to the 7-methyl guanosine cap of mRNA. Plants have an isozyme form of eIF4F (eIFiso4F) with comparable subunits, eIFiso4E and eIFiso4G. Plant eIF4A is very loosely associated with the plant cap-binding complexes. The specificity of interaction of the individual subunits of the two complexes was previously unknown. To address this issue, mixed complexes (eIF4E-eIFiso4G or eIFiso4E-eIF4G) were expressed and purified from Escherichia coli for biochemical analysis. The activity of the mixed complexes in in vitro translation assays correlated with the large subunit of the respective correct complex. These results suggest that the eIF4G or eIFiso4G subunits influence translational efficiency more than the cap-binding subunits. The translation assays also showed varying responses of the mRNA templates to eIF4F or eIFiso4F, suggesting that some level of mRNA discrimination is possible. The dissociation constants for the correct complexes have K(D) values in the subnanomolar range, whereas the mixed complexes were found to have K(D) values in the ∼10 nm range. Displacement assays showed that the correct binding partner readily displaces the incorrect binding partner in a manner consistent with the difference in K(D) values. These results show molecular specificity for the formation of plant eIF4F and eIFiso4F complexes and suggest a role in mRNA discrimination during initiation of translation.
真核生物翻译的起始需要一套 eIF,包括帽结合复合物 eIF4F。eIF4F 由 eIF4G 和 eIF4E 亚基组成,通常还有解旋酶 eIF4A。eIF4G 亚基作为其他起始因子的组装点,而 eIF4E 结合到 mRNA 的 7-甲基鸟苷帽上。植物具有与 eIF4F(eIFiso4F)类似的亚基的同工型(eIFiso4F),即 eIFiso4E 和 eIFiso4G。植物 eIF4A 与植物帽结合复合物的结合非常松散。两个复合物的各个亚基之间相互作用的特异性以前是未知的。为了解决这个问题,从大肠杆菌中表达和纯化了混合复合物(eIF4E-eIFiso4G 或 eIFiso4E-eIF4G)进行生化分析。混合复合物在体外翻译测定中的活性与相应正确复合物的大亚基相关。这些结果表明,eIF4G 或 eIFiso4G 亚基对翻译效率的影响大于帽结合亚基。翻译测定还表明,mRNA 模板对 eIF4F 或 eIFiso4F 的反应不同,这表明可能存在一定程度的 mRNA 区分。正确复合物的解离常数(K(D)值)在亚纳摩尔范围内,而混合复合物的 K(D)值在 10nm 左右。置换测定表明,正确的结合配偶体很容易以与 K(D)值差异一致的方式置换不正确的结合配偶体。这些结果表明植物 eIF4F 和 eIFiso4F 复合物的形成具有分子特异性,并提示在翻译起始过程中在 mRNA 区分中起作用。