Laboratory of Protein and Nucleic Acid Chemistry, The Rockefeller University, New York, United States.
Proteomics Resource Center, The Rockefeller University, New York, United States.
Elife. 2019 Jun 17;8:e45185. doi: 10.7554/eLife.45185.
Eukaryotic ribosome biogenesis is initiated with the transcription of pre-ribosomal RNA at the 5' external transcribed spacer, which directs the early association of assembly factors but is absent from the mature ribosome. The subsequent co-transcriptional association of ribosome assembly factors with pre-ribosomal RNA results in the formation of the small subunit processome. Here we show that stable rRNA domains of the small ribosomal subunit can independently recruit their own biogenesis factors in vivo. The final assembly and compaction of the small subunit processome requires the presence of the 5' external transcribed spacer RNA and all ribosomal RNA domains. Additionally, our cryo-electron microscopy structure of the earliest nucleolar pre-ribosomal assembly - the 5' external transcribed spacer ribonucleoprotein - provides a mechanism for how conformational changes in multi-protein complexes can be employed to regulate the accessibility of binding sites and therefore define the chronology of maturation events during early stages of ribosome assembly.
真核生物核糖体生物发生是从 5' 外部转录间隔区的 pre-rRNA 转录开始的,该转录区指导装配因子的早期结合,但不存在于成熟核糖体中。随后,核糖体装配因子与 pre-rRNA 的共转录结合导致小亚基加工体的形成。在这里,我们表明小核糖体亚基的稳定 rRNA 结构域可以在体内独立招募它们自己的生物发生因子。小亚基加工体的最终组装和压缩需要 5' 外部转录间隔区 RNA 和所有 rRNA 结构域的存在。此外,我们的最早核仁 pre-rRNA 组装的冷冻电子显微镜结构——5' 外部转录间隔区核糖核蛋白——提供了一种机制,即多蛋白复合物中的构象变化如何被用来调节结合位点的可及性,从而定义核糖体组装早期阶段成熟事件的时间顺序。