核糖体
生物
泛素连接酶
真核小核糖体亚单位
泛素
核糖体蛋白
细胞生物学
核糖体RNA
核糖体分析
遗传学
真核核糖体
核糖核酸
基因
作者
Elayanambi Sundaramoorthy,Marilyn Leonard,Raymond Mak,Jingwen Liao,Amit Fulzele,Eric J. Bennett
出处
期刊:Molecular Cell
[Elsevier]
日期:2017-02-01
卷期号:65 (4): 751-760.e4
被引量:266
标识
DOI:10.1016/j.molcel.2016.12.026
摘要
Ribosomes that experience terminal stalls during translation are resolved by ribosome-associated quality control (QC) pathways that oversee mRNA and nascent chain destruction and recycle ribosomal subunits. The proximal factors that sense stalled ribosomes and initiate mammalian ribosome-associated QC events remain undefined. We demonstrate that the ZNF598 ubiquitin ligase and the 40S ribosomal protein RACK1 help to resolve poly(A)-induced stalled ribosomes. They accomplish this by regulating distinct and overlapping regulatory 40S ribosomal ubiquitylation events. ZNF598 primarily mediates regulatory ubiquitylation of RPS10 and RPS20, whereas RACK1 regulates RPS2, RPS3, and RPS20 ubiquitylation. Gain or loss of ZNF598 function or mutations that block RPS10 or RPS20 ubiquitylation result in defective resolution of stalled ribosomes and subsequent readthrough of poly(A)-containing stall sequences. Together, our results indicate that ZNF598, RACK1, and 40S regulatory ubiquitylation plays a pivotal role in mammalian ribosome-associated QC pathways.
科研通智能强力驱动
Strongly Powered by AbleSci AI