Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Biomolecules. 2024 Aug 9;14(8):975. doi: 10.3390/biom14080975.
Here we review the functions of ribosomal proteins (RPs) in the nucleolar stages of large ribosomal subunit assembly in the yeast . We summarize the effects of depleting RPs on pre-rRNA processing and turnover, on the assembly of other RPs, and on the entry and exit of assembly factors (AFs). These results are interpreted in light of recent near-atomic-resolution cryo-EM structures of multiple assembly intermediates. Results are discussed with respect to each neighborhood of RPs and rRNA. We identify several key mechanisms related to RP behavior. Neighborhoods of RPs can assemble in one or more than one step. Entry of RPs can be triggered by molecular switches, in which an AF is replaced by an RP binding to the same site. To drive assembly forward, rRNA structure can be stabilized by RPs, including clamping rRNA structures or forming bridges between rRNA domains.
在这里,我们回顾了核糖体蛋白 (RP) 在酵母大亚基组装的核仁阶段的功能。我们总结了耗尽 RP 对前 rRNA 加工和周转、其他 RP 组装以及组装因子 (AF) 的进入和退出的影响。这些结果是根据多个组装中间体的近原子分辨率冷冻电镜结构来解释的。结果根据 RP 和 rRNA 的每个邻域进行了讨论。我们确定了与 RP 行为相关的几个关键机制。RP 的邻域可以分一步或多步组装。RP 的进入可以通过分子开关触发,其中一个 AF 被与同一位点结合的 RP 取代。为了推动组装前进,可以通过 RP 稳定 rRNA 结构,包括夹断 rRNA 结构或在 rRNA 结构域之间形成桥。