Lawson T G, Ray B K, Dodds J T, Grifo J A, Abramson R D, Merrick W C, Betsch D F, Weith H L, Thach R E
J Biol Chem. 1986 Oct 25;261(30):13979-89.
The effects of 5' proximal secondary structure in mRNA molecules on their translation and on their interaction with the eukaryotic initiation factors (eIF)-4F, eIF-4A, and eIF-4B have been examined. Secondary structures were generated in the 5' noncoding region of rabbit globin and reovirus mRNAs by means of hybridization with cDNA molecules. cDNAs hybridized to the first 15 bases downstream from the cap inhibited the translation of the mRNAs in both reticulocyte and wheat germ lysates. The degree of inhibition was directly related to the monovalent ion concentration and inversely related to reaction temperature. These hybrid structures also reduced the competitive ability of the messages. Hybrid structures beginning downstream from the first 15 bases did not inhibit the translation of beta-globin mRNA or reovirus s3 mRNA. None of the hybrid structures were detrimental to the interaction of the mRNAs with the 26-kDa cap binding protein of eIF-4F, as determined by chemical cross-linking assays. However, in the presence of ATP, hybrid structures immediately adjacent to the cap severely inhibited the cross-linking to the p46 subunit of eIF-4F or to additional eIF-4A or eIF-4B. In order to account for these observations, a two-step mechanism is proposed for the interaction of eIF-4F with the 5' end of an mRNA molecule. The first step involves a weak initial interaction of the p26 subunit with the cap. The second step requires the hydrolysis of ATP and results in the formation of a stable initiation factor-mRNA complex, which may involve eIF-4A and eIF-4B. This second step is inhibited by the presence of 5' proximal secondary structure. In any event, our results demonstrate that the effect of mRNA structure on translation rate depends strongly on its position with respect to the 5' end and that this effect is due at least in part to an inhibition of the action of initiation factors normally required for the unwinding of structure.
已对mRNA分子中5'近端二级结构对其翻译以及与真核起始因子(eIF)-4F、eIF-4A和eIF-4B相互作用的影响进行了研究。通过与cDNA分子杂交,在兔珠蛋白和呼肠孤病毒mRNA的5'非编码区产生二级结构。与帽下游前15个碱基杂交的cDNA在网织红细胞和小麦胚芽裂解物中均抑制mRNA的翻译。抑制程度与单价离子浓度直接相关,与反应温度呈负相关。这些杂交结构也降低了信息的竞争能力。从第15个碱基下游开始的杂交结构不抑制β-珠蛋白mRNA或呼肠孤病毒s3 mRNA的翻译。化学交联分析表明,没有一种杂交结构对mRNA与eIF-4F的26 kDa帽结合蛋白的相互作用有害。然而,在ATP存在的情况下,紧邻帽的杂交结构严重抑制与eIF-4F的p46亚基或额外的eIF-4A或eIF-4B的交联。为了解释这些观察结果,提出了一种eIF-4F与mRNA分子5'末端相互作用的两步机制。第一步涉及p26亚基与帽的弱初始相互作用。第二步需要ATP水解,并导致形成稳定的起始因子-mRNA复合物,这可能涉及eIF-4A和eIF-4B。第二步受到5'近端二级结构的抑制。无论如何,我们的结果表明,mRNA结构对翻译速率的影响在很大程度上取决于其相对于5'末端的位置,并且这种影响至少部分是由于抑制了通常用于解开结构的起始因子的作用。