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Nucleolus

About: Nucleolus is a research topic. Over the lifetime, 5873 publications have been published within this topic receiving 232435 citations. The topic is also known as: GO:0005730 & cell nucleolus.


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Journal ArticleDOI
TL;DR: It is demonstrated that the largest subunit of RNA polymerase I, RPA194, was coimmunoprecipitated with the human Nopp140 (hNopp140) and such an interaction is mediated through amino acids 204 to 382 of h nopp140, suggesting that Nopp 140 can interact with RNA polymerases I in vivo.
Abstract: Nopp140 is thought to shuttle between nucleolus and cytoplasm. However, the predominant nucleolar localization of Nopp140 homologues from different species suggests that Nopp140 is also involved in events occurring within the nucleolus. In this study, we demonstrated that the largest subunit of RNA polymerase I, RPA194, was coimmunoprecipitated with the human Nopp140 (hNopp140). Such an interaction is mediated through amino acids 204 to 382 of hNopp140. By double immunofluorescence, hNopp140 was colocalized with RNA polymerase I at the rDNA (rRNA genes) transcription active foci in the nucleolus. These results suggest that Nopp140 can interact with RNA polymerase I in vivo. Transfected cells expressing the amino-terminal half of hNopp140, hNopp140N382 (amino acids 1 to 382), displayed altered nucleoli with crescent-shaped structures. This phenotype is reminiscent of the segregated nucleoli induced by actinomycin D treatment, which is known to inhibit rRNA synthesis. Consistently, the hNopp140N382 protein mislocalized the endogenous RNA polymerase I and shut off cellular rRNA gene transcription as revealed by an in situ run-on assay. These dominant negative effects of the mutant hNopp140N382 suggest that Nopp140 plays an essential role in rDNA transcription. Interestingly, ectopic expression of hNopp140 to a very high level caused the formation of a transcriptionally inactive spherical structure occupying the entire nucleolar area which trapped the RNA polymerase I, fibrillarin, and hNopp140 but excluded the nucleolin. The mislocalizations of these nucleolar proteins after hNopp140 overexpression imply that Nopp140 may also play roles in maintenance of nucleolar integrity. The nucleolus in eukaryotic cells carries out most of the important reactions in ribosome biogenesis, including rDNA (rRNA genes) transcription, rRNA processing, and preribosome assembly (34, 47, 49, 50). Elements of nucleolar architecture mediate a tight temporal and topological orchestration of these processes. In higher eukaryotic cells, nucleoli exhibit a common organization consisting of three ultrastructurally distinct regions, the fibrillar center (FC), the dense fibrillar component (DFC), and the granular component (GC). The main body of the nucleolus is made up of the GC, embedded in this granular mass are several islets of rounded structures, FCs, each surrounded by a compact layer of the DFC. Tandemly repeated rRNA genes are clustered mostly in the FCs (42, 57), with transcription occurring largely at the boundary between the FC and the DFC (13, 20, 42, 58). Nascent rRNA transcripts are processed in the DFC (25, 38, 59). Some processing steps may also occur in the GC, together with the assembly of the mature rRNA and ribosomal proteins into preribosomal subunits (42, 47). In addition to rDNA, rRNA, and ribosomal proteins, the nucleolus harbors a large number of nonribosomal proteins and small nucleolar RNAs, which mediate the transcriptional and posttranscriptional reactions of ribosome biogenesis (49, 54). Many nucleolar proteins locate in particular nucleolar regions, which may reflect functional compart

99 citations

Journal ArticleDOI
TL;DR: A maize genetic marker strain was found to carry a cytologically-visible “duplication” of the nucleolar organizer region (NOR), and the chromosomal site of DNA complementary to rRNA was shown to be localized in the NOR, the first report on the localization of rDNA cistrons in theNOR of plants.
Abstract: A maize genetic marker strain (designated as the 2NOR strain) was found to carry a cytologically-visible “duplication” of the nucleolar organizer region (NOR). The 2 NOR condition is a simply inherited cytological marker which is transmitted normally through mega- and microsporogenesis and is associated when homozygous with a nucleolus approximately 64% greater in volume than that of two representative normal inbred lines of maize.—Utilizing DNA · rRNA hybridization techniques and the 2 NOR strain plus two unrelated inbred lines with normal NOR's, the chromosomal site of DNA complementary to rRNA was shown to be localized in the NOR. To our knowledge, this is the first report on the localization of rDNA cistrons in the NOR of plants. An estimate was made of 17,000 rDNA cistrons per diploid nucleus for normal maize.—The 2 NOR strain was shown to possess approximately twice as many rDNA cistrons (34,000) as normal maize. The usefulness of this 2 NOR condition for plant protein improvement programs is being investigated.

99 citations

Journal ArticleDOI
TL;DR: Improvements in mass spectrometry technologies, the characterization of protein complexes, and data mining will assist in furthering the understanding of the role of nucleoli in different physiological and pathological cell states.
Abstract: Nucleoli are plurifunctional nuclear domains involved in the regulation of several major cellular processes such as ribosome biogenesis, the biogenesis of non-ribosomal ribonucleoprotein complexes, cell cycle, and cellular aging. Until recently, the protein content of nucleoli was poorly described. Several proteomic analyses have been undertaken to discover the molecular bases of the biological roles fulfilled by nucleoli. These studies have led to the identification of more than 700 proteins. Extensive bibliographic and bioinformatic analyses allowed the classification of the identified proteins into functional groups and suggested potential functions of 150 human proteins previously uncharacterized. The combination of improvements in mass spectrometry technologies, the characterization of protein complexes, and data mining will assist in furthering our understanding of the role of nucleoli in different physiological and pathological cell states.

99 citations

Journal ArticleDOI
TL;DR: Dyskerin gene silencing in the MCF‐7 human breast carcinoma cell line reduced telomerase activity and rRNA pseudo‐uridylation, and patients with low dyskerin expression were characterized by a better clinical outcome than those with a high Dyskerin level.
Abstract: Dyskerin is a nucleolar protein, altered in dyskeratosis congenita, which carries out two separate functions, both fundamental for proliferating cells. One function is the pseudo-uridylation of ribosomal RNA (rRNA) molecules, necessary for their processing, and the other is the stabilization of the telomerase RNA component, necessary for telomerase activity. A significant feature of dyskeratosis congenita is an increased susceptibility to cancer; so far, however, no data have been reported on dyskerin changes in human tumours. Therefore, in this study, the distribution of dyskerin in a large series of human tumours from the lung, breast, and colon, as well as from B-cell lymphomas, was analysed by immunohistochemistry. Dyskerin proved never to be lost or delocalized outside the nucleolus. A quantitative analysis of dyskerin mRNA expression was then performed in 70 breast carcinomas together with the evaluation of telomerase RNA component levels and rRNA pseudo-uridylation. Dyskerin mRNA levels were highly variable and directly associated with both telomerase RNA component levels and rRNA pseudo-uridylation. Dyskerin gene silencing in the MCF-7 human breast carcinoma cell line reduced telomerase activity and rRNA pseudo-uridylation. Significantly, patients with low dyskerin expression were characterized by a better clinical outcome than those with a high dyskerin level. These data indicate that dyskerin is not lost in human cancers and that the levels of its expression and function are associated with tumour progression.

99 citations

Journal ArticleDOI
TL;DR: It is shown with chromosomal immunostaining and in situ hybridization that ribosomal subunits are present at transcription sites of Drosophila salivary gland chromosomes, and kinetics of recruitment following transcription initiation suggest that the association is with newly transcribed pol II transcripts.

99 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023145
2022209
2021143
2020125
2019139
2018121