H/ACA snoRNP guides ribosomal RNA subdomain folding in a satellite particle before joining the core 90S pre-ribosome

Paulina Fischer, Matthias Thoms, Benjamin Lau, Timo Denk, Maria Kuvshinova, Otto Berninghausen, Dirk Flemming, Ed Hurt, Roland Beckmann
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Abstract

During synthesis, modification and maturation of the ribosomal RNA, correct subdomain folding without additional guidance poses a major challenge. An essential H/ACA snoRNP, snR30, was observed to be outsourced from the core of the 90S, the earliest known pre-ribosome, to form a "satellite particle". This particle interacts with the so-called 18S rRNA platform subdomain, guiding its independent folding through localized structural interactions. Once this subdomain achieves its proper conformation, it is integrated into the core pre-ribosome, contributing to the overall maturation of the 18S rRNA. By temporarily segregating the folding process within a specialized satellite particle, the correct assembly of individual components is facilitated, thereby reducing the risk of errors during the complex process of ribosome assembly. In a broader sense, molecular outsourcing in cellular processes, where transient subcomplexes handle specific tasks before rejoining the main assembly line, can enhance efficiency and accuracy of complex molecular processes like ribosome biogenesis.
H/ACA snoRNP 引导核糖体 RNA 亚域在卫星颗粒中折叠,然后加入核心 90S 前核糖体
在核糖体 RNA 的合成、修饰和成熟过程中,在没有额外指导的情况下正确折叠亚域是一项重大挑战。据观察,一种重要的 H/ACA snoRNP(snR30)从已知最早的前核糖体 90S 的核心外包出去,形成一种 "卫星颗粒"。这种粒子与所谓的 18S rRNA 平台亚域相互作用,通过局部结构相互作用引导其独立折叠。一旦这个亚域达到适当的构象,它就会被整合到核心前核糖体中,促进 18S rRNA 的整体成熟。通过将折叠过程暂时隔离在一个专门的卫星颗粒内,可以促进单个成分的正确组装,从而降低核糖体复杂组装过程中出现错误的风险。从广义上讲,细胞过程中的分子外包,即在重新加入主装配线之前,由瞬时亚复合物处理特定任务,可以提高核糖体生物发生等复杂分子过程的效率和准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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