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环境线索诱导核仁的长非编码 RNA 依赖性重塑。

Environmental cues induce a long noncoding RNA-dependent remodeling of the nucleolus.

机构信息

Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

出版信息

Mol Biol Cell. 2013 Sep;24(18):2943-53. doi: 10.1091/mbc.E13-04-0223. Epub 2013 Jul 31.

Abstract

The nucleolus is a plurifunctional organelle in which structure and function are intimately linked. Its structural plasticity has long been appreciated, particularly in response to transcriptional inhibition and other cellular stresses, although the mechanism and physiological relevance of these phenomena are unclear. Using MCF-7 and other mammalian cell lines, we describe a structural and functional adaptation of the nucleolus, triggered by heat shock or physiological acidosis, that depends on the expression of ribosomal intergenic spacer long noncoding RNA (IGS lncRNA). At the heart of this process is the de novo formation of a large subnucleolar structure, termed the detention center (DC). The DC is a spatially and dynamically distinct region, characterized by an 8-anilino-1-naphthalenesulfonate-positive hydrophobic signature. Its formation is accompanied by redistribution of nucleolar factors and arrest in ribosomal biogenesis. Silencing of regulatory IGS lncRNA prevents the creation of this structure and allows the nucleolus to retain its tripartite organization and transcriptional activity. Signal termination causes a decrease in IGS transcript levels and a return to the active nucleolar conformation. We propose that the induction of IGS lncRNA by environmental signals operates as a molecular switch that regulates the structure and function of the nucleolus.

摘要

核仁是一个多功能细胞器,其结构和功能密切相关。其结构的可塑性早已被人们所认识,特别是在转录抑制和其他细胞应激反应中,但这些现象的机制和生理相关性尚不清楚。我们使用 MCF-7 和其他哺乳动物细胞系,描述了核仁的一种结构和功能的适应性变化,这种变化是由热休克或生理酸中毒触发的,依赖于核糖体基因间间隔长非编码 RNA(IGS lncRNA)的表达。这个过程的核心是一个新形成的大亚核仁结构,称为滞留中心(DC)。DC 是一个在空间和动态上都有区别的区域,其特征是 8-苯胺-1-萘磺酸阳性的疏水性特征。其形成伴随着核仁因子的重新分布和核糖体生物发生的停滞。调节 IGS lncRNA 的沉默阻止了这种结构的形成,并使核仁保持其三分体结构和转录活性。信号终止导致 IGS 转录本水平降低,并恢复到活跃的核仁构象。我们提出,环境信号诱导 IGS lncRNA 的表达,作为一种分子开关,调节核仁的结构和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d959/3771955/d878f9ec6884/2943fig1.jpg

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