Literature DB >> 15561100

Nuclear RNAs confined to a reticular compartment between chromosome territories.

Joanna M Bridger1, Claudia Kalla, Harald Wodrich, Sandra Weitz, Jason A King, Khashayarsha Khazaie, Hans-Georg Kräusslich, Peter Lichter.   

Abstract

RNA polymerase II transcripts are confined to nuclear compartments. A detailed analysis of the nuclear topology of RNA from individual genes was performed for transcripts from the marker gene coding for chloramphenicol acetyltransferase, expressed at a high level from the HTLV-1 LTR promoter. The construct was transfected into A293 cells where the RNA was organized as an extensive reticular network. We also studied the RNA distribution from combinations of neighboring HIV and bacterial resistance genes that co-integrated within the genome of COS-7 cells-revealing spherical or track-like accumulations of RNA that were extensively branched. There were many nuclei with distinct but overlapping RNA accumulations. Since the coding genes localized at the overlapping points, the RNAs are synthesized at a common region and diverge. The correlation between the frequency of the separation of the transcripts and the physical distance of the respective genes suggests a subcompartmentalization in the microenvironment of genes on the basis of geometric parameters. Thus, the more distant the genes are on the same chromosome, the more likely they are confined to separated subcompartments of an extensive reticular system. Co-delineation of the RNA transcripts with Cajal bodies and chromosome territories indicated the organization of nuclear RNA transcripts in a reticular interchromosome domain compartment.

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Year:  2005        PMID: 15561100     DOI: 10.1016/j.yexcr.2004.07.038

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  12 in total

Review 1.  Chromosome territories.

Authors:  Thomas Cremer; Marion Cremer
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03       Impact factor: 10.005

2.  Mechanism of mRNA transport in the nucleus.

Authors:  Diana Y Vargas; Arjun Raj; Salvatore A E Marras; Fred Russell Kramer; Sanjay Tyagi
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-11       Impact factor: 11.205

Review 3.  Mobility of multi-subunit complexes in the nucleus: accessibility and dynamics of chromatin subcompartments.

Authors:  Sabine M Görisch; Peter Lichter; Karsten Rippe
Journal:  Histochem Cell Biol       Date:  2005-04-14       Impact factor: 4.304

Review 4.  The genome and the nucleus: a marriage made by evolution. Genome organisation and nuclear architecture.

Authors:  Helen A Foster; Joanna M Bridger
Journal:  Chromosoma       Date:  2005-10-15       Impact factor: 4.316

Review 5.  Dynamics of transcription and mRNA export.

Authors:  Xavier Darzacq; Robert H Singer; Yaron Shav-Tal
Journal:  Curr Opin Cell Biol       Date:  2005-06       Impact factor: 8.382

Review 6.  Gene expression within a dynamic nuclear landscape.

Authors:  Yaron Shav-Tal; Xavier Darzacq; Robert H Singer
Journal:  EMBO J       Date:  2006-07-13       Impact factor: 11.598

7.  Single-cell c-myc gene expression in relationship to nuclear domains.

Authors:  Eva Bártová; Andrea Harnicarová; Jana Krejcí; Ludek Strasák; Stanislav Kozubek
Journal:  Chromosome Res       Date:  2008-03-07       Impact factor: 5.239

Review 8.  The coming-of-age of nucleocytoplasmic transport in motor neuron disease and neurodegeneration.

Authors:  Paulo A Ferreira
Journal:  Cell Mol Life Sci       Date:  2019-02-11       Impact factor: 9.261

Review 9.  The dynamic pathway of nuclear RNA in eukaryotes.

Authors:  Jonathan Sheinberger; Yaron Shav-Tal
Journal:  Nucleus       Date:  2013-04-11       Impact factor: 4.197

10.  Protein Tpr is required for establishing nuclear pore-associated zones of heterochromatin exclusion.

Authors:  Sandra Krull; Julia Dörries; Björn Boysen; Sonja Reidenbach; Lars Magnius; Helene Norder; Johan Thyberg; Volker C Cordes
Journal:  EMBO J       Date:  2010-04-20       Impact factor: 11.598

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