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聚合酶I转录与加工的核仁结构

The nucleolar architecture of polymerase I transcription and processing.

作者信息

Shaw P J, Highett M I, Beven A F, Jordan E G

机构信息

Department of Cell Biology, John Innes Centre, Colney, Norwich, UK.

出版信息

EMBO J. 1995 Jun 15;14(12):2896-906. doi: 10.1002/j.1460-2075.1995.tb07289.x.

Abstract

The nucleolus, the site of transcription and processing of the major ribosomal genes, generally reveals three distinct ultrastructural components in conventional thin-section electron micrographs (fibrillar centres, dense fibrillar component and granular component). We show here that different parts of the transcription and transcript processing pathway can be mapped to the different nucleolar components in pea root cells. This study shows the full three-dimensional arrangement of the different domains by in situ hybridization and confocal microscopy, and their correspondence with the major ultrastructural components of the nucleolus is revealed by parallel serial section electron microscopy. The active rDNA is widely dispersed in discrete foci, the larger of which, at least, correspond to well-defined fibrillar centres. A probe to the external transcribed spacer (ETS) sequence of the pre-rRNA transcripts labels clearly demarcated regions surrounding the foci of rDNA, and which we show correspond to the dense fibrillar component. Finally, a probe to the entire 45S transcript shows a higher concentration in regions corresponding to the granular component, surrounding the dense fibrillar component labelled by the ETS probe. The changes in structure that occur with heat shock show that nucleolar organization is dynamic and dependent upon transcriptional activity. These results show that the various RNA processing events are spatially highly organized and suggest a vectorial or radial model of transcription and transcript processing, where nascent and newly completed transcripts occupy zones surrounding the genes, which are in turn surrounded by regions containing the older more mature transcripts.

摘要

核仁是主要核糖体基因转录和加工的场所,在传统的超薄切片电子显微镜图像中,通常显示出三种不同的超微结构成分(纤维中心、致密纤维组分和颗粒组分)。我们在此表明,转录和转录本加工途径的不同部分可以映射到豌豆根细胞中的不同核仁组分上。本研究通过原位杂交和共聚焦显微镜展示了不同结构域的完整三维排列,并通过平行连续切片电子显微镜揭示了它们与核仁主要超微结构组分的对应关系。活跃的核糖体DNA广泛分散在离散的位点上,其中至少较大的位点对应于明确的纤维中心。针对前体核糖体RNA转录本外部转录间隔区(ETS)序列的探针清晰地标记了核糖体DNA位点周围界限分明的区域,我们发现这些区域对应于致密纤维组分。最后,针对整个45S转录本的探针在对应于颗粒组分的区域中显示出较高的浓度,该区域围绕着由ETS探针标记的致密纤维组分。热激引起的结构变化表明核仁组织是动态的,并且依赖于转录活性。这些结果表明,各种RNA加工事件在空间上高度有序,并提示了一种转录和转录本加工的矢量或径向模型,即新生和新完成的转录本占据基因周围的区域,而这些区域又被包含更老、更成熟转录本的区域所包围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c6c/398408/8e0d19e8c83c/emboj00036-0222-a.jpg

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