UPS写了一个新的传奇故事

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et Biophysica Acta-Gene Regulatory Mechanisms Pub Date : 2023-08-30 DOI:10.1016/j.bbagrm.2023.194981
Priyanka Barman, Pritam Chakraborty, Rhea Bhaumik, Sukesh R. Bhaumik
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引用次数: 1

摘要

SAGA (Spt-Ada-Gcn5-Acetyltransferase)是一种进化保守的真核生物转录共激活因子,是一种大型多亚基蛋白复合物,具有两种不同的酶活性,即组蛋白乙酰转移酶HAT (Histone acetyltransferase)和去泛素酶DUB (De-ubiquitinase),由基因特异性激活蛋白靶向组蛋白共价修饰和PIC (Pre-initiation complex)形成,以增强转录(或基因激活)。26S蛋白酶体(通过泛素化参与蛋白的靶向降解)的19S RP(调节颗粒)以不依赖蛋白水解的方式进一步促进了SAGA靶向基因启动子。此外,最近还发现,26S蛋白酶体通过其Sgf73/ataxin-7组分的泛素化以蛋白质水解依赖的方式调节SAGA,这是SAGA完整性和DUB活性(以及转录)所必需的,并且与包括神经退行性疾病和癌症在内的各种疾病有关。因此,SAGA本身及其对活性基因的靶向是由UPS(泛素-蛋白酶体系统)调控的,与疾病有关。
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UPS writes a new saga of SAGA

SAGA (Spt-Ada-Gcn5-Acetyltransferase), an evolutionarily conserved transcriptional co-activator among eukaryotes, is a large multi-subunit protein complex with two distinct enzymatic activities, namely HAT (Histone acetyltransferase) and DUB (De-ubiquitinase), and is targeted to the promoter by the gene-specific activator proteins for histone covalent modifications and PIC (Pre-initiation complex) formation in enhancing transcription (or gene activation). Targeting of SAGA to the gene promoter is further facilitated by the 19S RP (Regulatory particle) of the 26S proteasome (that is involved in targeted degradation of protein via ubiquitylation) in a proteolysis-independent manner. Moreover, SAGA is also recently found to be regulated by the 26S proteasome in a proteolysis-dependent manner via the ubiquitylation of its Sgf73/ataxin-7 component that is required for SAGA's integrity and DUB activity (and hence transcription), and is linked to various diseases including neurodegenerative disorders and cancer. Thus, SAGA itself and its targeting to the active gene are regulated by the UPS (Ubiquitin-proteasome system) with implications in diseases.

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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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