Literature DB >> 7060135

Stable transcription complexes of Xenopus 5S RNA genes: a means to maintain the differentiated state.

D F Bogenhagen, W M Wormington, D D Brown.   

Abstract

Cloned 5S RNA genes added to Xenopus oocyte nuclear extract assemble into stable active transcription complexes that persist for many rounds of 5S RNA synthesis. This stability of the complex has been demonstrated by its resistance to dilution and to competitor DNA. A stable complex is formed within minutes and lasts for at least 40 rounds of transcription per template over several hours. Stable, transcriptionally inactive complexes can be formed by incubation of cloned 5S RNA genes in an oocyte nuclear extract depleted of a 5S-specific transcription factor and supplemented with histones. The stable, transcriptionally active and inactive states of 5S RNA gene complexes that can be formed in vitro are analogous to the states of the somatic and oocyte 5S RNA genes as they exist in somatic cell chromatin. Oocyte 5S RNa genes remain repressed in chromatin isolated from somatic cells, but can be activated by washing chromatin with high salt. Maintenance of the differentiated state of cell requires that selected genes remain stably active while others are stably repressed for long periods of time. We propose that stable transcription complexes may play an important role in the maintenance of the differentiated state in eucaryotic cells.

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Year:  1982        PMID: 7060135     DOI: 10.1016/0092-8674(82)90359-2

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  137 in total

Review 1.  Survey and summary: transcription by RNA polymerases I and III.

Authors:  M R Paule; R J White
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

2.  Multiple, dispersed human U6 small nuclear RNA genes with varied transcriptional efficiencies.

Authors:  Angela M Domitrovich; Gary R Kunkel
Journal:  Nucleic Acids Res       Date:  2003-05-01       Impact factor: 16.971

3.  Chromosomal footprinting of transcriptionally active and inactive oocyte-type 5S RNA genes of Xenopus laevis.

Authors:  D R Engelke; J M Gottesfeld
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

4.  Transcription termination by RNA polymerase III: uncoupling of polymerase release from termination signal recognition.

Authors:  F E Campbell; D R Setzer
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

5.  Differential expression of oocyte-type class III genes with fraction TFIIIC from immature or mature oocytes.

Authors:  W F Reynolds; D L Johnson
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

6.  Multiple states of protein-DNA interaction in the assembly of transcription complexes on Saccharomyces cerevisiae 5S ribosomal RNA genes.

Authors:  B R Braun; D L Riggs; G A Kassavetis; E P Geiduschek
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

7.  Human TFIIIA alone is sufficient to prevent nucleosomal repression of a homologous 5S gene.

Authors:  W Stünkel; I Kober; M Kauer; G Taimor; K H Seifart
Journal:  Nucleic Acids Res       Date:  1995-01-11       Impact factor: 16.971

8.  Structure of the yeast TAP1 protein: dependence of transcription activation on the DNA context of the target gene.

Authors:  T L Aldrich; G Di Segni; B L McConaughy; N J Keen; S Whelen; B D Hall
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

9.  Detecting protein-DNA interactions in vivo: distribution of RNA polymerase on specific bacterial genes.

Authors:  D S Gilmour; J T Lis
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

10.  Cooperative model for the binding of Xenopus transcription factor A to the 5S RNA gene.

Authors:  J S Hanas; D F Bogenhagen; C W Wu
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

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