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酵母 18S rRNA 直接参与核糖体对翻译起始时严格 AUG 选择的反应。

Yeast 18 S rRNA is directly involved in the ribosomal response to stringent AUG selection during translation initiation.

机构信息

Molecular Cellular and Developmental Biology Program, Kansas State University, Manhattan, Kansas 66506, USA.

出版信息

J Biol Chem. 2010 Oct 15;285(42):32200-12. doi: 10.1074/jbc.M110.146662. Epub 2010 Aug 10.

Abstract

In eukaryotes, the 40 S ribosomal subunit serves as the platform of initiation factor assembly, to place itself precisely on the AUG start codon. Structural arrangement of the 18 S rRNA determines the overall shape of the 40 S subunit. Here, we present genetic evaluation of yeast 18 S rRNA function using 10 point mutations altering the polysome profile. All the mutants reduce the abundance of the mutant 40 S, making it limiting for translation initiation. Two of the isolated mutations, G875A, altering the core of the platform domain that binds eIF1 and eIF2, and A1193U, changing the h31 loop located below the P-site tRNA(i)(Met), show phenotypes indicating defective regulation of AUG selection. Evidence is provided that these mutations reduce the interaction with the components of the preinitiation complex, thereby inhibiting its function at different steps. These results indicate that the 18 S rRNA mutations impair the integrity of scanning-competent preinitiation complex, thereby altering the 40 S subunit response to stringent AUG selection. Interestingly, nine of the mutations alter the body/platform domains of 18 S rRNA, potentially affecting the bridges to the 60 S subunit, but they do not change the level of 18 S rRNA intermediates. Based on these results, we also discuss the mechanism of the selective degradation of the mutant 40 S subunits.

摘要

在真核生物中,40S 核糖体亚基作为起始因子组装的平台,将自身精确地定位在 AUG 起始密码子上。18S rRNA 的结构排列决定了 40S 亚基的整体形状。在这里,我们使用改变多核糖体图谱的 10 个点突变来进行酵母 18S rRNA 功能的遗传评估。所有突变体都减少了突变体 40S 的丰度,使其成为翻译起始的限制因素。分离出的两个突变体,G875A 改变了与 eIF1 和 eIF2 结合的平台结构域核心,以及 A1193U 改变了位于 P 位 tRNA(i)(Met) 下方的 h31 环,表现出表明 AUG 选择调节缺陷的表型。有证据表明,这些突变降低了与起始前复合物成分的相互作用,从而在不同步骤抑制其功能。这些结果表明,18S rRNA 突变破坏了扫描能力起始前复合物的完整性,从而改变了 40S 亚基对严格的 AUG 选择的反应。有趣的是,九个突变改变了 18S rRNA 的主体/平台结构域,可能影响与 60S 亚基的桥接,但它们不改变 18S rRNA 中间产物的水平。基于这些结果,我们还讨论了突变体 40S 亚基选择性降解的机制。

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