去泛素酶OTUD1解决了多a和罕见的富含密码子的mrna上停滞的翻译。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Renata Snaurova, Alexander Vdovin, Michal Durech, Jakub Nezval, David Zihala, Tomas Jelinek, Roman Hajek, Michal Simicek
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引用次数: 1

摘要

OTUD1是一种去泛素化酶,参与许多细胞过程,包括癌症和先天免疫信号通路。在这里,我们进行了一项基于邻近标记的相互作用组研究,确定了OTUD1主要存在于翻译和RNA代谢蛋白复合物中。生化分析证实OTUD1与核糖体亚基、延伸因子和E3泛素连接酶ZNF598相关,但与翻译起始机制无关。OTUD1的催化活性通过抑制znf598介导的RPS10泛素化来抑制polyA触发的核糖体停滞,并刺激多聚体的形成。最后,基因表达分析表明OTUD1通过拮抗ZNF598调控稀有富密码子mrna的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deubiquitinase OTUD1 Resolves Stalled Translation on polyA and Rare Codon Rich mRNAs.

OTUD1 is a deubiquitinating enzyme involved in many cellular processes including cancer and innate, immune signaling pathways. Here, we perform a proximity labeling-based interactome study that identifies OTUD1 largely present in the translation and RNA metabolism protein complexes. Biochemical analysis validates OTUD1 association with ribosome subunits, elongation factors and the E3 ubiquitin ligase ZNF598 but not with the translation initiation machinery. OTUD1 catalytic activity suppresses polyA triggered ribosome stalling through inhibition of ZNF598-mediated RPS10 ubiquitination and stimulates formation of polysomes. Finally, analysis of gene expression suggests that OTUD1 regulates the stability of rare codon rich mRNAs by antagonizing ZNF598.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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