Suppr超能文献

ARF 介导的 Apak 的 SUMOylation 拮抗泛素化作用,并促进其核仁积累,以抑制 47S 前 rRNA 的合成。

ARF-mediated SUMOylation of Apak antagonizes ubiquitylation and promotes its nucleolar accumulation to inhibit 47S pre-rRNA synthesis.

机构信息

State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Collaborative Innovation Center for Cancer Medicine, Beijing 100850, China Institute of Cancer Stem Cell, Dalian Medical University, Dalian 116044, China.

Department of Biochemistry and Molecular Biology, Anhui Medical University, Hefei 230032, China.

出版信息

J Mol Cell Biol. 2015 Apr;7(2):154-67. doi: 10.1093/jmcb/mjv010. Epub 2015 Feb 17.

Abstract

Ribosomes are among the most fundamental molecular machines in all cells, as they are required for protein synthesis. Most structural rRNA components are generated in the nucleolus and assembled into pre-ribosomal particles. Here we show Apak, a previously identified p53 inhibitor, as a novel ribosomal stress response protein. In unstressed cells, Apak is bound to the deSUMOylase SENP1 in the nucleoplasm and targeted for proteasomal degradation by MDM2 ubiquitin ligase. Upon ribosomal stress, SENP1 dissociates from Apak and the tumor suppressor protein ARF couples Ubc9 with Apak to promote Apak SUMOylation on zinc fingers. This results in Apak protein stabilization and translocation to the nucleolus, where Apak inhibits the pre-rRNA synthesis. These findings provide a molecular mechanism whereby ARF coordinates Apak to regulate ribosome biogenesis upon cellular stress.

摘要

核糖体是所有细胞中最基本的分子机器之一,因为它们是蛋白质合成所必需的。大多数结构 rRNA 成分在核仁中生成,并组装成前核糖体颗粒。在这里,我们发现 Apak(一种先前被鉴定为 p53 抑制剂的蛋白)是一种新型核糖体应激反应蛋白。在未受应激的细胞中,Apak 与核质中的去 SUMO 酶 SENP1 结合,并被 MDM2 泛素连接酶靶向蛋白酶体降解。当核糖体受到应激时,SENP1 从 Apak 上解离,肿瘤抑制蛋白 ARF 将 Ubc9 与 Apak 连接起来,促进 Apak 锌指上的 SUMO 化。这导致 Apak 蛋白的稳定和向核仁的易位,在核仁中 Apak 抑制 pre-rRNA 的合成。这些发现提供了一个分子机制,即 ARF 协调 Apak 在细胞应激时调节核糖体生物发生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验