Cmarko D, Verschure P J, Martin T E, Dahmus M E, Krause S, Fu X D, van Driel R, Fakan S
Centre of Electron Microscopy, University of Lausanne, 1005 Lausanne, Switzerland.
Mol Biol Cell. 1999 Jan;10(1):211-23. doi: 10.1091/mbc.10.1.211.
In this study we demonstrate, at an ultrastructural level, the in situ distribution of heterogeneous nuclear RNA transcription sites after microinjection of 5-bromo-UTP (BrUTP) into the cytoplasm of living cells and subsequent postembedding immunoelectron microscopic visualization after different labeling periods. Moreover, immunocytochemical localization of several pre-mRNA transcription and processing factors has been carried out in the same cells. This high-resolution approach allowed us to reveal perichromatin regions as the most important sites of nucleoplasmic RNA transcription and the perichromatin fibrils (PFs) as in situ forms of nascent transcripts. Furthermore, we show that transcription takes place in a rather diffuse pattern, without notable local accumulation of transcription sites. RNA polymerase II, heterogeneous nuclear ribonucleoprotein (hnRNP) core proteins, general transcription factor TFIIH, poly(A) polymerase, splicing factor SC-35, and Sm complex of small nuclear ribonucleoproteins (snRNPs) are associated with PFs. This strongly supports the idea that PFs are also sites of major pre-mRNA processing events. The absence of nascent transcripts, RNA polymerase II, poly(A) polymerase, and hnRNPs within the clusters of interchromatin granules rules out the possibility that this domain plays a role in pre-mRNA transcription and polyadenylation; however, interchromatin granule-associated zones contain RNA polymerase II, TFIIH, and Sm complex of snRNPs and, after longer periods of BrUTP incubation, also Br-labeled RNA. Their role in nuclear functions still remains enigmatic. In the nucleolus, transcription sites occur in the dense fibrillar component. Our fine structural results show that PFs represent the major nucleoplasmic structural domain involved in active pre-mRNA transcriptional and processing events.
在本研究中,我们在超微结构水平上展示了将5-溴尿苷三磷酸(BrUTP)显微注射到活细胞胞质中,并在不同标记时间段后进行包埋后免疫电子显微镜观察,异质性核RNA转录位点的原位分布。此外,还在相同细胞中对几种前体mRNA转录和加工因子进行了免疫细胞化学定位。这种高分辨率方法使我们能够揭示染色质周区域是核质RNA转录的最重要位点,以及染色质周纤维(PFs)是新生转录本的原位形式。此外,我们表明转录以相当弥散的模式发生,转录位点没有明显的局部积累。RNA聚合酶II、异质性核核糖核蛋白(hnRNP)核心蛋白、通用转录因子TFIIH、聚腺苷酸聚合酶、剪接因子SC-35以及小核核糖核蛋白(snRNPs)的Sm复合物与PFs相关联。这有力地支持了PFs也是主要前体mRNA加工事件发生位点的观点。染色质间颗粒簇内不存在新生转录本、RNA聚合酶II、聚腺苷酸聚合酶和hnRNPs,排除了该区域在前体mRNA转录和聚腺苷酸化中起作用的可能性;然而,染色质间颗粒相关区域含有RNA聚合酶II、TFIIH和snRNPs的Sm复合物,并且在较长时间的BrUTP孵育后,还含有Br标记的RNA。它们在核功能中的作用仍然不明。在核仁中,转录位点出现在致密纤维成分中。我们的精细结构结果表明,PFs代表参与活跃前体mRNA转录和加工事件的主要核质结构域。