Literature DB >> 3600631

Transcription of adenovirus 2 major late and peptide IX genes under conditions of in vitro nucleosome assembly.

T Matsui.   

Abstract

Plasmid DNA containing adenovirus 2 major late and peptide IX genes was assembled into nucleosomes in vitro, and the assembled nucleosomes were used as a template to study the regulatory mechanism of transcription initiation under these conditions. Neither the major late nor peptide IX genes was transcribed on the already-assembled nucleosomes. However, the major late gene, but not the peptide IX gene, was transcribed efficiently when the DNA was incubated with HeLa cell extracts prior to assembly into nucleosomes. These results indicate that prebinding of some component in the cell extracts to DNA is essential to activate transcription of the major late gene on nucleosomes assembled under the conditions used here. Since gene IX on the nucleosomes was not transcriptionally active regardless of preincubation of DNA with the extracts, some other component or another, different template structure which is not able to be identified in an in vitro system with deproteinized DNA template might be required for activation of peptide IX gene transcription. To know the function of the upstream sequences of the major late gene, effects of the deletion on transcription of nucleosomes were compared with that of deproteinized DNA. The result showed that depression of transcription by deleting the upstream sequences had more effect on nucleosomes than on deproteinized DNA.

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Year:  1987        PMID: 3600631      PMCID: PMC365227          DOI: 10.1128/mcb.7.4.1401-1408.1987

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


  62 in total

1.  The presence of nucleosomes on a DNA template prevents initiation by RNA polymerase II in vitro.

Authors:  J A Knezetic; D S Luse
Journal:  Cell       Date:  1986-04-11       Impact factor: 41.582

2.  The SV40 72 bp repeat preferentially potentiates transcription starting from proximal natural or substitute promoter elements.

Authors:  B Wasylyk; C Wasylyk; P Augereau; P Chambon
Journal:  Cell       Date:  1983-02       Impact factor: 41.582

3.  An altered DNA conformation detected by S1 nuclease occurs at specific regions in active chick globin chromatin.

Authors:  A Larsen; H Weintraub
Journal:  Cell       Date:  1982-06       Impact factor: 41.582

4.  Sequences upstream from the T-A-T-A box are required in vivo and in vitro for efficient transcription from the adenovirus serotype 2 major late promoter.

Authors:  R Hen; P Sassone-Corsi; J Corden; M P Gaub; P Chambon
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

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

Authors:  D F Bogenhagen; W M Wormington; D D Brown
Journal:  Cell       Date:  1982-02       Impact factor: 41.582

6.  Structure of the active nucleolar chromatin of Xenopus laevis Oocytes.

Authors:  P Labhart; T Koller
Journal:  Cell       Date:  1982-02       Impact factor: 41.582

7.  Separation and characterization of factors mediating accurate transcription by RNA polymerase II.

Authors:  M Samuels; A Fire; P A Sharp
Journal:  J Biol Chem       Date:  1982-12-10       Impact factor: 5.157

8.  In vitro accurate initiation of transcription on the adenovirus type 2 IVa2 gene which does not contain a TATA box.

Authors:  T Matsui
Journal:  Nucleic Acids Res       Date:  1982-11-25       Impact factor: 16.971

9.  A small segment of polyoma virus DNA enhances the expression of a cloned beta-globin gene over a distance of 1400 base pairs.

Authors:  J de Villiers; W Schaffner
Journal:  Nucleic Acids Res       Date:  1981-12-11       Impact factor: 16.971

10.  Assembly of transcriptionally active 5S RNA gene chromatin in vitro.

Authors:  J Gottesfeld; L S Bloomer
Journal:  Cell       Date:  1982-04       Impact factor: 41.582

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  36 in total

1.  Heat shock-regulated transcription in vitro from a reconstituted chromatin template.

Authors:  P B Becker; S K Rabindran; C Wu
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-15       Impact factor: 11.205

2.  Upstream activation sequence-dependent alteration of chromatin structure and transcription activation of the yeast GAL1-GAL10 genes.

Authors:  M J Fedor; R D Kornberg
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

Review 3.  Relationship of eukaryotic DNA replication to committed gene expression: general theory for gene control.

Authors:  L P Villarreal
Journal:  Microbiol Rev       Date:  1991-09

4.  Transcriptional potentiation of the vitellogenin B1 promoter by a combination of both nucleosome assembly and transcription factors: an in vitro dissection.

Authors:  B Corthésy; P Léonnard; W Wahli
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

5.  Functional analysis of histones H2A and H2B in transcriptional repression in Saccharomyces cerevisiae.

Authors:  J Recht; B Dunn; A Raff; M A Osley
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

6.  SWI-SNF complex participation in transcriptional activation at a step subsequent to activator binding.

Authors:  M P Ryan; R Jones; R H Morse
Journal:  Mol Cell Biol       Date:  1998-04       Impact factor: 4.272

7.  Gal4p-mediated chromatin remodeling depends on binding site position in nucleosomes but does not require DNA replication.

Authors:  M Xu; R T Simpson; M P Kladde
Journal:  Mol Cell Biol       Date:  1998-03       Impact factor: 4.272

8.  Pathways of nucleoprotein assembly on 5S RNA genes in a Xenopus oocyte S-150 extract.

Authors:  M A Razik; J Blanco; J M Gottesfeld
Journal:  Nucleic Acids Res       Date:  1989-06-12       Impact factor: 16.971

9.  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

10.  Nucleosome loss activates CUP1 and HIS3 promoters to fully induced levels in the yeast Saccharomyces cerevisiae.

Authors:  L K Durrin; R K Mann; M Grunstein
Journal:  Mol Cell Biol       Date:  1992-04       Impact factor: 4.272

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