Literature DB >> 9694810

Transcriptionally active Xenopus laevis somatic 5 S ribosomal RNA genes are packaged with hyperacetylated histone H4, whereas transcriptionally silent oocyte genes are not.

L Howe1, T A Ranalli, C D Allis, J Ausió.   

Abstract

The relationship between histone acetylation and transcription of the Xenopus laevis oocyte and somatic 5 S ribosomal RNA genes was investigated. Chromatin fragments from a X. laevis kidney cell line were immunoprecipitated with an antibody specific for hyperacetylated histone H4. The DNA from the hyperacetylated chromatin was probed with both oocyte- and somatic gene-specific sequences, and the results showed that the upstream, nontranscribed region of the transcriptionally active somatic genes is packaged with acetylated histone H4. In contrast, the corresponding region of the transcriptionally silent oocyte genes is packaged with hypoacetylated histone H4 in this cells line. Further study also showed that this region of the oocyte genes was less sensitive to digestion with the enzyme, micrococcal nuclease. Together these results suggest that, as described for both RNA polymerase I and II transcribed genes, there is a correlation between histone acetylation and transcription of the RNA polymerase III transcribed 5 S ribosomal RNA genes in X. laevis.

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Year:  1998        PMID: 9694810     DOI: 10.1074/jbc.273.33.20693

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

1.  Rearrangement of chromatin domains during development in Xenopus.

Authors:  Y Vassetzky; A Hair; M Méchali
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

2.  The H3-H4 N-terminal tail domains are the primary mediators of transcription factor IIIA access to 5S DNA within a nucleosome.

Authors:  J M Vitolo; C Thiriet; J J Hayes
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

3.  Effects of histone tail domains on the rate of transcriptional elongation through a nucleosome.

Authors:  R U Protacio; G Li; P T Lowary; J Widom
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

4.  Hyperacetylation of chromatin at the ADH2 promoter allows Adr1 to bind in repressed conditions.

Authors:  Loredana Verdone; Jiansheng Wu; Kristen van Riper; Nataly Kacherovsky; Maria Vogelauer; Elton T Young; Michael Grunstein; Ernesto Di Mauro; Micaela Caserta
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

5.  Structural features of transcription factor IIIA bound to a nucleosome in solution.

Authors:  Joseph M Vitolo; Zungyoon Yang; Ravi Basavappa; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

6.  The core histone N-terminal tail domains negatively regulate binding of transcription factor IIIA to a nucleosome containing a 5S RNA gene via a novel mechanism.

Authors:  Zungyoon Yang; Chunyang Zheng; Christophe Thiriet; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2005-01       Impact factor: 4.272

7.  Different functional modes of p300 in activation of RNA polymerase III transcription from chromatin templates.

Authors:  Claudia Mertens; Robert G Roeder
Journal:  Mol Cell Biol       Date:  2008-07-21       Impact factor: 4.272

8.  Small ubiquitin-like modifier (SUMO)-mediated repression of the Xenopus Oocyte 5 S rRNA genes.

Authors:  Mariam Q Malik; Michelle M Bertke; Paul W Huber
Journal:  J Biol Chem       Date:  2014-11-03       Impact factor: 5.157

9.  The TFIIIC90 subunit of TFIIIC interacts with multiple components of the RNA polymerase III machinery and contains a histone-specific acetyltransferase activity.

Authors:  Y J Hsieh; T K Kundu; Z Wang; R Kovelman; R G Roeder
Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

10.  Human DNA ligase I efficiently seals nicks in nucleosomes.

Authors:  D R Chafin; J M Vitolo; L A Henricksen; R A Bambara; J J Hayes
Journal:  EMBO J       Date:  2000-10-16       Impact factor: 11.598

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