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Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum

机译:没有TQ(CUG)的真核生物:依赖于植物抑制性的TICTYOSTELIUM Discoideum中的依赖性TRNA修饰的作用

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摘要

In the Elongator-dependent modification pathway, chemical modifications are introduced at the wobble uridines at position 34 in transfer RNAs (tRNAs), which serve to optimize codon translation rates. Here, we show that this three-step modification pathway exists in Dictyostelium discoideum, model of the evolutionary superfamily Amoebozoa. Not only are previously established modifications observable by mass spectrometry in strains with the most conserved genes of each step deleted, but also additional modifications are detected, indicating a certain plasticity of the pathway in the amoeba. Unlike described for yeast, D. discoideum allows for an unconditional deletion of the single tO(CUG) gene, as long as the Elongator-dependent modification pathway is intact. In gene deletion strains of the modification pathway, protein amounts are significantly reduced as shown by flow cytometry and Western blotting, using strains expressing different glutamine leader constructs fused to GFP. Most dramatic are these effects, when the tQ(CUG) gene is deleted, or Elp3, the catalytic component of the Elongator complex is missing. In addition, Elp3 is the most strongly conserved protein of the modification pathway, as our phylogenetic analysis reveals. The implications of this observation are discussed with respect to the evolutionary age of the components acting in the Elongator-dependent modification pathway.
机译:在依赖于细胞依赖性修饰途径中,在转移RNA(TRNA)的位置34的摆动尿嘧啶处引入化学修饰,其用于优化密码子平移速率。在这里,我们表明,这种三步修改途径存在于dictyostelium discoideum,进化超家族amoeboozoa的模型中。此前不仅建立了通过菌株中的质谱法可观察到的各个步骤中最保守的基因,而且检测另外的修饰,表明Amoeba中的途径的某种可塑性。与酵母中描述的不同,D. discoideum允许无条件缺失单个至(Cug)基因,只要依赖于细胞依赖性修饰途径完好无损。在改性途径的基因缺失菌株中,使用流式细胞术和Western印迹显示的蛋白质量显着降低,所述蛋白质印迹,所述菌株表达与GFP融合的不同的谷氨酰胺引导构建体。大多数戏剧性的是这些效果,当缺失TQ(CUG)基因或ELP3时,缺少细长络合物的催化组分。此外,随着我​​们的系统发育分析显示,ELP3是改性途径最强烈的蛋白质。关于在依赖于细胞依赖性修饰途径中作用的组分的进化年龄,讨论了该观察结果的影响。

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  • 来源
    《Nucleic Acids Research》 |2020年第14期|共15页
  • 作者单位

    Jacobs Univ Bremen gGmbH Ribogenet Biochem Lab Dept Life Sci &

    Chem DE-28759 Bremen Germany;

    Jacobs Univ Bremen gGmbH Ribogenet Biochem Lab Dept Life Sci &

    Chem DE-28759 Bremen Germany;

    Univ Cambridge Dept Med Cambridge Biomed Campus Cambridge CB2 0QQ England;

    Univ Kassel Fachgebiet Mikrobiol Inst Biol Heinrich Plett Str 40 D-34132 Kassel Germany;

    Univ Kassel Fachgebiet Mikrobiol Inst Biol Heinrich Plett Str 40 D-34132 Kassel Germany;

    Ludwig Maximilians Univ Munchen Dept Chem &

    Pharm Butenandtstr 5-13 D-81377 Munich Germany;

    Jacobs Univ Bremen gGmbH Ribogenet Biochem Lab Dept Life Sci &

    Chem DE-28759 Bremen Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
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