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真核生物中没有 tQCUG:伸长因子依赖的 tRNA 修饰在盘基网柄菌中的作用。

Eukaryotic life without tQCUG: the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum.

机构信息

Ribogenetics Biochemistry Lab, Department of Life Sciences and Chemistry, Jacobs University Bremen gGmbH, DE 28759 Bremen, Germany.

Department of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK.

出版信息

Nucleic Acids Res. 2020 Aug 20;48(14):7899-7913. doi: 10.1093/nar/gkaa560.

Abstract

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 tQCUG 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 tQCUG 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.

摘要

在延伸因子依赖性修饰途径中,化学修饰被引入到 tRNA(转移 RNA)的摆动尿嘧啶 34 位,这有助于优化密码子翻译率。在这里,我们表明,这种三步修饰途径存在于变形虫模型进化超级家族变形虫中。不仅在删除每个步骤中最保守基因的菌株中可以通过质谱观察到以前建立的修饰,而且还检测到了其他修饰,表明该途径在变形虫中具有一定的可塑性。与酵母不同,只要延伸因子依赖性修饰途径完整,D. discoideum 就可以无条件删除单个 tQCUG 基因。在修饰途径的基因缺失菌株中,如通过流式细胞术和 Western blot 所示,使用表达不同谷氨酰胺前导序列融合 GFP 的菌株,蛋白含量显著降低。当删除 tQCUG 基因或缺失延伸因子复合物的催化成分 Elp3 时,这些影响最为明显。此外,Elp3 是修饰途径中最保守的蛋白质,正如我们的系统发育分析所揭示的那样。讨论了这一观察结果对在延伸因子依赖性修饰途径中起作用的组分的进化年龄的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/7430636/4591dccd5de0/gkaa560fig1.jpg

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