Literature DB >> 9234694

Nucleosomal structures of c-myc promoters with transcriptionally engaged RNA polymerase II.

T Albert1, J Mautner, J O Funk, K Hörtnagel, A Pullner, D Eick.   

Abstract

Organization of DNA into chromatin has been shown to contribute to a repressed state of gene transcription. Disruption of nucleosomal structure is observed in response to gene induction, suggesting a model in which RNA polymerase II (pol II) is recruited to the promoter upon reorganization of nucleosomes. Here we show that induction of c-myc transcription correlates with the disruption of two nucleosomes in the upstream promoter region. This nucleosomal disruption, however, is not necessary for the binding of pol II to the promoter. Transcriptionally engaged pol II complexes can be detected when the upstream chromatin is in a more closed configuration. Thus, upstream chromatin opening is suggested to affect activation of promoter-bound pol II rather than entry of polymerases into the promoter. Interestingly, pol II complexes are detectable in both sense and antisense transcriptional directions, but only complexes in the sense direction respond to activation signals resulting in processive transcription.

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Year:  1997        PMID: 9234694      PMCID: PMC232290          DOI: 10.1128/MCB.17.8.4363

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  79 in total

1.  Regulation of c-myc transcription in vitro: dependence on the guanine-rich promoter element ME1a1.

Authors:  D J Hall
Journal:  Oncogene       Date:  1990-01       Impact factor: 9.867

Review 2.  Transcription elongation and eukaryotic gene regulation.

Authors:  C A Spencer; M Groudine
Journal:  Oncogene       Date:  1990-06       Impact factor: 9.867

Review 3.  Regulation of gene expression by nucleosomes.

Authors:  J Svaren; W Hörz
Journal:  Curr Opin Genet Dev       Date:  1996-04       Impact factor: 5.578

4.  The block of elongation in c-myc exon 1 is abolished in Burkitt's lymphoma cell lines with variant translocation.

Authors:  D Eick; A Polack; E Kofler; G W Bornkamm
Journal:  Oncogene       Date:  1988-10       Impact factor: 9.867

5.  Chromatin remodeling during Saccharomyces cerevisiae ADH2 gene activation.

Authors:  L Verdone; G Camilloni; E Di Mauro; M Caserta
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

6.  Postinitiation transcriptional control in Drosophila melanogaster.

Authors:  A E Rougvie; J T Lis
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

7.  Nucleosome positioning modulates accessibility of regulatory proteins to the mouse mammary tumor virus promoter.

Authors:  B Piña; U Brüggemeier; M Beato
Journal:  Cell       Date:  1990-03-09       Impact factor: 41.582

8.  HSF access to heat shock elements in vivo depends critically on promoter architecture defined by GAGA factor, TFIID, and RNA polymerase II binding sites.

Authors:  L S Shopland; K Hirayoshi; M Fernandes; J T Lis
Journal:  Genes Dev       Date:  1995-11-15       Impact factor: 11.361

9.  NF-kappa B-mediated chromatin reconfiguration and transcriptional activation of the HIV-1 enhancer in vitro.

Authors:  M J Pazin; P L Sheridan; K Cannon; Z Cao; J G Keck; J T Kadonaga; K A Jones
Journal:  Genes Dev       Date:  1996-01-01       Impact factor: 11.361

10.  Transcriptional activation and chromatin remodeling of the HIV-1 promoter in response to histone acetylation.

Authors:  C Van Lint; S Emiliani; M Ott; E Verdin
Journal:  EMBO J       Date:  1996-03-01       Impact factor: 11.598

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  6 in total

1.  Loss of FBP function arrests cellular proliferation and extinguishes c-myc expression.

Authors:  L He; J Liu; I Collins; S Sanford; B O'Connell; C J Benham; D Levens
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

2.  Characterization of the TATA-less core promoter of the cell cycle-regulated cdc25C gene.

Authors:  K Körner; L A Wolfraim; F C Lucibello; R Müller
Journal:  Nucleic Acids Res       Date:  1997-12-15       Impact factor: 16.971

3.  Transcriptional consequences of topoisomerase inhibition.

Authors:  I Collins; A Weber; D Levens
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

4.  Cdk7 is required for full activation of Drosophila heat shock genes and RNA polymerase II phosphorylation in vivo.

Authors:  Brian E Schwartz; Stephane Larochelle; Beat Suter; John T Lis
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

5.  The immunoglobulin heavy chain locus control region increases histone acetylation along linked c-myc genes.

Authors:  L Madisen; A Krumm; T R Hebbes; M Groudine
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

6.  Transition from initiation to promoter proximal pausing requires the CTD of RNA polymerase II.

Authors:  C Lux; H Albiez; R D Chapman; M Heidinger; M Meininghaus; R Brack-Werner; A Lang; M Ziegler; T Cremer; D Eick
Journal:  Nucleic Acids Res       Date:  2005-09-12       Impact factor: 16.971

  6 in total

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