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25S rRNA A 环与真核翻译起始因子 5B 的相互作用促进亚基结合并确保严格的 AUG 选择。

Interaction between 25S rRNA A loop and eukaryotic translation initiation factor 5B promotes subunit joining and ensures stringent AUG selection.

机构信息

Molecular Cellular and Developmental Biology Program, Kansas State University, Manhattan, Kansas, USA.

出版信息

Mol Cell Biol. 2013 Sep;33(18):3540-8. doi: 10.1128/MCB.00771-13. Epub 2013 Jul 8.

Abstract

In yeast, 25S rRNA makes up the major mass and shape of the 60S ribosomal subunit. During the last step of translation initiation, eukaryotic initiation factor 5B (eIF5B) promotes the 60S subunit joining with the 40S initiation complex (IC). Malfunctional 60S subunits produced by misfolding or mutation may disrupt the 40S IC stalling on the start codon, thereby altering the stringency of initiation. Using several point mutations isolated by random mutagenesis, here we studied the role of 25S rRNA in start codon selection. Three mutations changing bases near the ribosome surface had strong effects, allowing the initiating ribosomes to skip both AUG and non-AUG codons: C2879U and U2408C, altering the A loop and P loop, respectively, of the peptidyl transferase center, and G1735A, mapping near a Eukarya-specific bridge to the 40S subunit. Overexpression of eIF5B specifically suppressed the phenotype caused by C2879U, suggesting functional interaction between eIF5B and the A loop. In vitro reconstitution assays showed that C2879U decreased eIF5B-catalyzed 60S subunit joining with a 40S IC. Thus, eIF5B interaction with the peptidyl transferase center A loop increases the accuracy of initiation by stabilizing the overall conformation of the 80S initiation complex. This study provides an insight into the effect of ribosomal mutations on translation profiles in eukaryotes.

摘要

在酵母中,25S rRNA 构成了 60S 核糖体亚基的主要质量和形状。在翻译起始的最后一步,真核起始因子 5B(eIF5B)促进 60S 亚基与 40S 起始复合物(IC)结合。折叠或突变导致功能失调的 60S 亚基可能会破坏 40S IC 在起始密码子上的停滞,从而改变起始的严格性。本研究使用随机诱变分离的几个点突变,研究了 25S rRNA 在起始密码子选择中的作用。三个改变核糖体表面附近碱基的突变具有很强的影响,允许起始核糖体跳过 AUG 和非 AUG 密码子:C2879U 和 U2408C 分别改变了肽转移酶中心的 A 环和 P 环,而 G1735A 映射到真核生物特有的桥接附近到 40S 亚基。eIF5B 的过表达特异性抑制了 C2879U 引起的表型,表明 eIF5B 和 A 环之间存在功能相互作用。体外重建实验表明,C2879U 降低了 eIF5B 催化的 60S 亚基与 40S IC 的结合。因此,eIF5B 与肽转移酶中心 A 环的相互作用通过稳定 80S 起始复合物的整体构象,提高了起始的准确性。这项研究为核糖体突变对真核生物翻译谱的影响提供了新的见解。

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