The versatility of the proteasome in gene expression and silencing: Unraveling proteolytic and non-proteolytic functions

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et Biophysica Acta-Gene Regulatory Mechanisms Pub Date : 2023-08-24 DOI:10.1016/j.bbagrm.2023.194978
Hyesu Lee , Sungwook Kim , Daeyoup Lee
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Abstract

The 26S proteasome consists of a 20S core particle and a 19S regulatory particle and critically regulates gene expression and silencing through both proteolytic and non-proteolytic functions. The 20S core particle mediates proteolysis, while the 19S regulatory particle performs non-proteolytic functions. The proteasome plays a role in regulating gene expression in euchromatin by modifying histones, activating transcription, initiating and terminating transcription, mRNA export, and maintaining transcriptome integrity. In gene silencing, the proteasome modulates the heterochromatin formation, spreading, and subtelomere silencing by degrading specific proteins and interacting with anti-silencing factors such as Epe1, Mst2, and Leo1. This review discusses the proteolytic and non-proteolytic functions of the proteasome in regulating gene expression and gene silencing-related heterochromatin formation. This article is part of a special issue on the regulation of gene expression and genome integrity by the ubiquitin-proteasome system.

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蛋白酶体在基因表达和沉默中的多功能性:揭示蛋白水解和非蛋白水解功能
26S蛋白酶体由一个20S核心颗粒和一个19S调控颗粒组成,通过蛋白水解和非蛋白水解功能对基因表达和沉默进行关键调控。20S核心颗粒介导蛋白水解,而19S调节颗粒执行非蛋白水解功能。蛋白酶体通过修饰组蛋白、激活转录、启动和终止转录、mRNA输出和维持转录组完整性来调节常染色质中的基因表达。在基因沉默中,蛋白酶体通过降解特定蛋白并与抗沉默因子(如Epe1、Mst2和Leo1)相互作用来调节异染色质的形成、扩散和亚端粒沉默。本文综述了蛋白酶体在调节基因表达和基因沉默相关异染色质形成中的蛋白水解和非蛋白水解功能。本文是泛素-蛋白酶体系统调控基因表达和基因组完整性专题的一部分。
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来源期刊
CiteScore
9.20
自引率
2.10%
发文量
63
审稿时长
44 days
期刊介绍: BBA Gene Regulatory Mechanisms includes reports that describe novel insights into mechanisms of transcriptional, post-transcriptional and translational gene regulation. Special emphasis is placed on papers that identify epigenetic mechanisms of gene regulation, including chromatin, modification, and remodeling. This section also encompasses mechanistic studies of regulatory proteins and protein complexes; regulatory or mechanistic aspects of RNA processing; regulation of expression by small RNAs; genomic analysis of gene expression patterns; and modeling of gene regulatory pathways. Papers describing gene promoters, enhancers, silencers or other regulatory DNA regions must incorporate significant functions studies.
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