The nucleolus: Coordinating stress response and genomic stability

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Katiuska González-Arzola
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引用次数: 0

Abstract

The perception that the nucleoli are merely the organelles where ribosome biogenesis occurs is challenged. Only around 30 % of nucleolar proteins are solely involved in producing ribosomes. Instead, the nucleolus plays a critical role in controlling protein trafficking during stress and, according to its dynamic nature, undergoes continuous protein exchange with nucleoplasm under various cellular stressors. Hence, the concept of nucleolar stress has evolved as cellular insults that disrupt the structure and function of the nucleolus. Considering the emerging role of this organelle in DNA repair and the fact that rDNAs are the most fragile genomic loci, therapies targeting the nucleoli are increasingly being developed. Besides, drugs that target ribosome synthesis and induce nucleolar stress can be used in cancer therapy. In contrast, agents that regulate nucleolar activity may be a potential treatment for neurodegeneration caused by abnormal protein accumulation in the nucleolus. Here, I explore the roles of nucleoli beyond their ribosomal functions, highlighting the factors triggering nucleolar stress and their impact on genomic stability.

核仁:协调应激反应和基因组稳定性
核小体仅仅是核糖体生物发生的细胞器这一观点受到了质疑。只有约 30% 的核小体蛋白质只参与核糖体的生成。相反,核小体在应激过程中控制蛋白质运输方面起着至关重要的作用,而且根据其动态性质,在各种细胞应激因素下,核小体与核质之间会不断进行蛋白质交换。因此,核小体应激的概念演变为破坏核小体结构和功能的细胞损伤。考虑到这一细胞器在 DNA 修复中新出现的作用,以及 rDNA 是最脆弱的基因组位点这一事实,针对核小体的疗法正被越来越多地开发出来。此外,针对核糖体合成和诱导核小体应激的药物也可用于癌症治疗。与此相反,调节核小体活性的药物可能是治疗核小体蛋白质异常积累导致的神经变性的潜在疗法。在此,我将探讨核小体在核糖体功能之外的作用,重点介绍引发核小体应激的因素及其对基因组稳定性的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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