Dasso M C, Milburn S C, Hershey J W, Jackson R J
Department of Biochemistry, University of Cambridge, England.
Eur J Biochem. 1990 Jan 26;187(2):361-71. doi: 10.1111/j.1432-1033.1990.tb15313.x.
A cDNA clone of the influenza virus NS (non-structural protein) gene in a vector carrying a bacteriophage T7 RNA polymerase promoter was manipulated so as to reiterate the initiation site to give two in-frame AUG codons 57 nucleotide residues apart. Each initiation site was in either a preferred context (...AUAAUGG...) or a less favourable context (...UUUAUGG...) and the four possible permutations were constructed. When capped mRNA transcripts of these clones were translated in the rabbit reticulocyte lysate system, products from initiation at both AUG codons were observed. At low RNA concentrations the frequency of initiation at the 5'-proximal AUG codon rather than the second was higher when the first AUG codon was in the preferred context, in qualitative agreement with the scanning ribosome model. However, a completely unexpected finding was that the ratio of initiation at the first AUG codon to initiation at the second decreased with increasing mRNA concentration, irrespective of the particular context involved. Several lines of evidence indicated that the increased frequency of initiation at the second AUG codon was not due solely to the lower density of ribosome loading per mRNA at high RNA concentrations, and may therefore be the result of high RNA concentrations out-titring the capacity of endogenous reticulocyte factors responsible for preferential initiation at the 5'-proximal AUG codon. The effect of supplementing the system with purified initiation factors was examined. Only eIF-2 was capable of decreasing the frequency of initiation at the second AUG codon and promoting use of the first AUG at high mRNA concentrations; eIF-3, 4A, 4B, 4C + 4D, 4F and 5 were inactive.
对携带噬菌体T7 RNA聚合酶启动子的载体中的流感病毒NS(非结构蛋白)基因的cDNA克隆进行操作,使起始位点重复,产生两个框内AUG密码子,相隔57个核苷酸残基。每个起始位点要么处于优选的上下文(...AUAAUGG...),要么处于不太有利的上下文(...UUUAUGG...),并构建了四种可能的排列。当这些克隆的加帽mRNA转录本在兔网织红细胞裂解物系统中进行翻译时,观察到了两个AUG密码子起始产生的产物。在低RNA浓度下,当第一个AUG密码子处于优选上下文时,5'-近端AUG密码子而非第二个AUG密码子的起始频率更高,这与扫描核糖体模型在定性上一致。然而,一个完全出乎意料的发现是,无论涉及何种特定上下文,第一个AUG密码子的起始与第二个AUG密码子的起始之比都随着mRNA浓度的增加而降低。几条证据表明,第二个AUG密码子起始频率的增加不仅仅是由于高RNA浓度下每个mRNA上核糖体负载密度较低,因此可能是高RNA浓度超过了负责在5'-近端AUG密码子优先起始的内源性网织红细胞因子的能力的结果。研究了用纯化的起始因子补充该系统的效果。只有eIF-2能够降低第二个AUG密码子的起始频率,并在高mRNA浓度下促进第一个AUG的使用;eIF-3、4A、4B、4C + 4D、4F和5没有活性。