Department of Integrative Structural and Computational Biology, The Scripps Research Institute, Jupiter, FL.
Howard Hughes Medical Institute, Chevy Chase, MD.
J Cell Biol. 2020 Nov 2;219(11). doi: 10.1083/jcb.202004161.
During translation initiation, 40S ribosomes scan the mRNA until they encounter the start codon, where conformational changes produce a translation-competent 80S complex. Destabilizing the scanning complex results in misinitiation at non-AUG codons, demonstrating its importance for fidelity. Here, we use a combination of biochemical and genetic analyses to demonstrate that the ability of the nascent subunit to adopt the scanning complex is tested during assembly via structural mimicry. Specifically, formation of the 80S-like assembly intermediate, which structurally resembles scanning complexes, requires the correct folding of two rRNA elements in the subunit head and the proper positioning of the universally conserved head proteins Rps3, Rps15, Rps20, and Rps29. rRNA misfolding impairs the formation of 80S-like ribosomes, and bypass of individual checkpoints using cancer-associated mutations produces ribosomes defective in accurate start-site selection. Thus, the formation of 80S-like assembly intermediates is a quality control step that ensures scanning competence of the nascent subunit.
在翻译起始过程中,40S 核糖体扫描 mRNA,直到它们遇到起始密码子,此时构象变化产生具有翻译能力的 80S 复合物。破坏扫描复合物会导致非 AUG 密码子的错误起始,这表明其对保真度很重要。在这里,我们使用生化和遗传分析的组合来证明,在组装过程中,通过结构模拟来测试新生亚基采用扫描复合物的能力。具体来说,形成类似于扫描复合物的 80S 样组装中间体需要亚基头部中的两个 rRNA 元件的正确折叠以及普遍保守的头部蛋白 Rps3、Rps15、Rps20 和 Rps29 的正确定位。rRNA 错误折叠会损害 80S 样核糖体的形成,并且使用癌症相关突变绕过单个检查点会产生起始位点选择不准确的核糖体缺陷。因此,形成 80S 样组装中间体是一个质量控制步骤,可确保新生亚基的扫描能力。