Literature DB >> 8320255

Fluorescent labeling of nascent RNA reveals transcription by RNA polymerase II in domains scattered throughout the nucleus.

D G Wansink1, W Schul, I van der Kraan, B van Steensel, R van Driel, L de Jong.   

Abstract

Several nuclear activities and components are concentrated in discrete nuclear compartments. To understand the functional significance of nuclear compartmentalization, knowledge on the spatial distribution of transcriptionally active chromatin is essential. We have examined the distribution of sites of transcription by RNA polymerase II (RPII) by labeling nascent RNA with 5-bromouridine 5'-triphosphate, in vitro and in vivo. Nascent RPII transcripts were found in over 100 defined areas, scattered throughout the nucleoplasm. No preferential localization was observed in either the nuclear interior or the periphery. Each transcription site may represent the activity of a single gene or, considering the number of active pre-mRNA genes in a cell, of a cluster of active genes. The relation between the distribution of nascent RPII transcripts and that of the essential splicing factor SC-35 was investigated in double labeling experiments. Antibodies against SC-35 recognize a number of well-defined, intensely labeled nuclear domains, in addition to labeling of more diffuse areas between these domains (Spector, D. L., X. -D. Fu, and T. Maniatis. 1991. EMBO (Eur. Mol. Biol. Organ.) J. 10:3467-3481). We observe no correlation between intensely labeled SC-35 domains and sites of pre-mRNA synthesis. However, many sites of RPII synthesis colocalize with weakly stained areas. This implies that contranscriptional splicing takes place in these weakly stained areas. These areas may also be sites where splicing is completed posttranscriptionally. Intensely labeled SC-35 domains may function as sites for assembly, storage, or regeneration of splicing components, or as compartments for degradation of introns.

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Year:  1993        PMID: 8320255      PMCID: PMC2119648          DOI: 10.1083/jcb.122.2.283

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  76 in total

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Journal:  Cytometry       Date:  1985-11

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Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

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  189 in total

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Authors:  J G Gall; M Bellini; Z Wu; C Murphy
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Journal:  Nucleic Acids Res       Date:  2000-05-15       Impact factor: 16.971

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4.  Nuclear pre-mRNA compartmentalization: trafficking of released transcripts to splicing factor reservoirs.

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Authors:  M Thiry; T Cheutin; M F O'Donohue; H Kaplan; D Ploton
Journal:  RNA       Date:  2000-12       Impact factor: 4.942

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Journal:  Mol Biol Cell       Date:  2000-08       Impact factor: 4.138

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Journal:  EMBO Rep       Date:  2001-11       Impact factor: 8.807

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Authors:  M Dundr; T Misteli
Journal:  Biochem J       Date:  2001-06-01       Impact factor: 3.857

9.  Histone H4 acetylation of euchromatin and heterochromatin is cell cycle dependent and correlated with replication rather than with transcription.

Authors:  Z Jasencakova; A Meister; J Walter; B M Turner; I Schubert
Journal:  Plant Cell       Date:  2000-11       Impact factor: 11.277

Review 10.  Genome-wide technology for determining RNA stability in mammalian cells: historical perspective and recent advantages based on modified nucleotide labeling.

Authors:  Hidenori Tani; Nobuyoshi Akimitsu
Journal:  RNA Biol       Date:  2012-10-01       Impact factor: 4.652

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