Literature DB >> 10773068

Spatial organization of RNA polymerase II transcription in the nucleus.

M N Szentirmay1, M Sawadogo.   

Abstract

In eukaryotic cells, mRNA synthesis is carried out by large, multifunctional complexes that are also involved in coordinating transcription with other nuclear processes. This survey focuses on the distribution and structural arrangement of these complexes within the nucleus, in relationship with the discrete positioning of particular chromosomal loci. To better understand the link between the spatial organization of the nucleus and the regulation of gene expression, it is necessary to combine information from biochemical studies with results from microscopic observations of preserved nuclear structures. Recent experimental approaches have made this possible. The subnuclear locations of specific chromosome loci, RNA transcripts, RNA polymerases, and transcription and pre-mRNA-processing factors can now be observed with computer-assisted microscopy and specific molecular probes. The results indicate that RNA polymerase II (RNAPII) transcription takes place at discrete sites scattered throughout the nucleoplasm, and that these sites are also the locations of pre-mRNA processing. Transcribing polymerases appear to be grouped into clusters at each transcription site. Cell cycle-dependent zones of transcription and processing factors have been identified, and certain subnuclear domains appear specialized for expression or silencing of particular genes. The arrangement of transcription in the nucleus is dynamic and depends on its transcriptional activity, with the RNAPII itself playing a central role in marshalling the large complexes involved in gene expression.

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Year:  2000        PMID: 10773068      PMCID: PMC105382          DOI: 10.1093/nar/28.10.2019

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  97 in total

1.  5'-Capping enzymes are targeted to pre-mRNA by binding to the phosphorylated carboxy-terminal domain of RNA polymerase II.

Authors:  S McCracken; N Fong; E Rosonina; K Yankulov; G Brothers; D Siderovski; A Hessel; S Foster; S Shuman; D L Bentley
Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

Review 2.  Transcription units as RNA processing units.

Authors:  K M Neugebauer; M B Roth
Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

3.  mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain.

Authors:  E J Cho; T Takagi; C R Moore; S Buratowski
Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

4.  Regional and temporal specialization in the nucleus: a transcriptionally-active nuclear domain rich in PTF, Oct1 and PIKA antigens associates with specific chromosomes early in the cell cycle.

Authors:  A Pombo; P Cuello; W Schul; J B Yoon; R G Roeder; P R Cook; S Murphy
Journal:  EMBO J       Date:  1998-03-16       Impact factor: 11.598

Review 5.  Thinking about a nuclear matrix.

Authors:  T Pederson
Journal:  J Mol Biol       Date:  1998-03-27       Impact factor: 5.469

Review 6.  A CTD function linking transcription to splicing.

Authors:  J L Corden; M Patturajan
Journal:  Trends Biochem Sci       Date:  1997-11       Impact factor: 13.807

7.  Association of transcriptionally silent genes with Ikaros complexes at centromeric heterochromatin.

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Journal:  Cell       Date:  1997-12-12       Impact factor: 41.582

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Authors:  A I Lamond; W C Earnshaw
Journal:  Science       Date:  1998-04-24       Impact factor: 47.728

9.  Growth-related changes in phosphorylation of yeast RNA polymerase II.

Authors:  M Patturajan; R J Schulte; B M Sefton; R Berezney; M Vincent; O Bensaude; S L Warren; J L Corden
Journal:  J Biol Chem       Date:  1998-02-20       Impact factor: 5.157

10.  Factors associated with the mammalian RNA polymerase II holoenzyme.

Authors:  A S Neish; S F Anderson; B P Schlegel; W Wei; J D Parvin
Journal:  Nucleic Acids Res       Date:  1998-02-01       Impact factor: 16.971

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  12 in total

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3.  Characterization of a natural heterodimer between MLV genomic RNA and the SD' retroelement generated by alternative splicing.

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Journal:  RNA       Date:  2007-10-10       Impact factor: 4.942

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Authors:  Fernando de Macedo Dossin; Sergio Schenkman
Journal:  Eukaryot Cell       Date:  2005-05

5.  Murine leukemia virus RNA dimerization is coupled to transcription and splicing processes.

Authors:  Stéphan Maurel; Marylène Mougel
Journal:  Retrovirology       Date:  2010-08-05       Impact factor: 4.602

6.  Novel DNA-binding properties of the RNA-binding protein TIAR.

Authors:  Esther A Suswam; Yan Yan Li; Harry Mahtani; Peter H King
Journal:  Nucleic Acids Res       Date:  2005-08-09       Impact factor: 16.971

Review 7.  Anchoring the genome.

Authors:  Diego Ottaviani; Elliott Lever; Petros Takousis; Denise Sheer
Journal:  Genome Biol       Date:  2008-01-22       Impact factor: 13.583

8.  Epigenetic silencing of the XAF1 gene is mediated by the loss of CTCF binding.

Authors:  Georgina Victoria-Acosta; Karla Vazquez-Santillan; Luis Jimenez-Hernandez; Laura Muñoz-Galindo; Vilma Maldonado; Gustavo Ulises Martinez-Ruiz; Jorge Melendez-Zajgla
Journal:  Sci Rep       Date:  2015-10-07       Impact factor: 4.379

9.  Evidence for transcriptional activity in the syncytiotrophoblast of the human placenta.

Authors:  P M Ellery; T Cindrova-Davies; E Jauniaux; A C Ferguson-Smith; G J Burton
Journal:  Placenta       Date:  2009-02-11       Impact factor: 3.481

10.  Diaphanous formin mDia2 regulates CENP-A levels at centromeres.

Authors:  Chenshu Liu; Yinghui Mao
Journal:  J Cell Biol       Date:  2016-05-16       Impact factor: 10.539

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