Laboratory of Protein and Nucleic Acid Chemistry, The Rockefeller University, New York, New York, USA; email:
Annu Rev Biochem. 2024 Aug;93(1):189-210. doi: 10.1146/annurev-biochem-030222-113611. Epub 2024 Jul 2.
During the last ten years, developments in cryo-electron microscopy have transformed our understanding of eukaryotic ribosome assembly. As a result, the field has advanced from a list of the vast array of ribosome assembly factors toward an emerging molecular movie in which individual frames are represented by structures of stable ribosome assembly intermediates with complementary biochemical and genetic data. In this review, we discuss the mechanisms driving the assembly of yeast and human small and large ribosomal subunits. A particular emphasis is placed on the most recent findings that illustrate key concepts of ribosome assembly, such as folding of preribosomal RNA, the enforced chronology of assembly, enzyme-mediated irreversible transitions, and proofreading of preribosomal particles.
在过去的十年中,冷冻电子显微镜的发展改变了我们对真核核糖体组装的理解。结果,该领域已经从核糖体组装因子的庞大列表发展到一个新兴的分子电影,其中单个帧由稳定的核糖体组装中间体的结构表示,这些结构具有互补的生化和遗传数据。在这篇综述中,我们讨论了驱动酵母和人类小和大亚基核糖体组装的机制。特别强调的是最近的发现,这些发现说明了核糖体组装的关键概念,如前核糖体 RNA 的折叠、组装的强制时间顺序、酶介导的不可逆转变以及前核糖体颗粒的校对。