Literature DB >> 1678348

Glucocorticoids are required for establishment and maintenance of an alteration in chromatin structure: induction leads to a reversible disruption of nucleosomes over an enhancer.

A Reik1, G Schütz, A F Stewart.   

Abstract

Induction of the rat tyrosine aminotransferase gene (TAT) with glucocorticoid hormones leads to formation of a nuclease hypersensitive site at the hormone-dependent enhancer located 2.5 kb upstream of the start site of transcription. This enhancer comprises binding sites for the glucocorticoid receptor and additional transcription factors which are only recognized after hormone administration, as demonstrated by genomic footprinting. We show here that the alteration in chromatin structure occurs very rapidly and is also rapidly reversible after withdrawal of the hormone. At all stages nuclease hypersensitivity at this enhancer parallels the transcriptional activity of the TAT gene indicating that transcriptional stimulation requires ongoing enhancer activity. The enhancer region is nucleosomal before induction and after removal of the hormone but the nucleosomal pattern is disturbed in the presence of the hormone. The rapidity of chromatin changes implies that neither disruption nor reassembly of the nucleosomes is dependent on DNA replication. Addition of the glucocorticoid antagonist RU486 to induced cells has effects similar to washing out the glucocorticoid hormone, showing that maintenance of the hypersensitive site requires the ongoing binding of agonist by glucocorticoid receptor. These results describe an inducible enhancer which is regulated by a dynamic balance between two types of protein-DNA complexes, one of which is nucleosomal.

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Year:  1991        PMID: 1678348      PMCID: PMC452954          DOI: 10.1002/j.1460-2075.1991.tb07797.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  67 in total

1.  Occupation of the c-fos serum response element in vivo by a multi-protein complex is unaltered by growth factor induction.

Authors:  R E Herrera; P E Shaw; A Nordheim
Journal:  Nature       Date:  1989-07-06       Impact factor: 49.962

2.  Nucleosomes inhibit the initiation of transcription but allow chain elongation with the displacement of histones.

Authors:  Y Lorch; J W LaPointe; R D Kornberg
Journal:  Cell       Date:  1987-04-24       Impact factor: 41.582

3.  Changes in histone gene dosage alter transcription in yeast.

Authors:  C D Clark-Adams; D Norris; M A Osley; J S Fassler; F Winston
Journal:  Genes Dev       Date:  1988-02       Impact factor: 11.361

4.  Cooperativity of glucocorticoid response elements located far upstream of the tyrosine aminotransferase gene.

Authors:  H M Jantzen; U Strähle; B Gloss; F Stewart; W Schmid; M Boshart; R Miksicek; G Schütz
Journal:  Cell       Date:  1987-04-10       Impact factor: 41.582

5.  In vivo protein-DNA interactions in a glucocorticoid response element require the presence of the hormone.

Authors:  P B Becker; B Gloss; W Schmid; U Strähle; G Schütz
Journal:  Nature       Date:  1986 Dec 18-31       Impact factor: 49.962

6.  Transcription activation of the tyrosine aminotransferase gene by glucocorticoids and cAMP in primary hepatocytes.

Authors:  E Schmid; W Schmid; M Jantzen; D Mayer; B Jastorff; G Schütz
Journal:  Eur J Biochem       Date:  1987-06-15

7.  Reprogramming cell differentiation in the absence of DNA synthesis.

Authors:  C P Chiu; H M Blau
Journal:  Cell       Date:  1984-07       Impact factor: 41.582

8.  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

9.  DNA sequences outside the receptor-binding sites differently modulate the responsiveness of the mouse mammary tumour virus promoter to various steroid hormones.

Authors:  A C Cato; P Skroch; J Weinmann; P Butkeraitis; H Ponta
Journal:  EMBO J       Date:  1988-05       Impact factor: 11.598

10.  Assembly of transfected DNA into chromatin: structural changes in the origin-promoter-enhancer region upon replication.

Authors:  S Cereghini; M Yaniv
Journal:  EMBO J       Date:  1984-06       Impact factor: 11.598

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  67 in total

1.  Asymmetric and node-specific nodal expression patterns are controlled by two distinct cis-acting regulatory elements.

Authors:  D P Norris; E J Robertson
Journal:  Genes Dev       Date:  1999-06-15       Impact factor: 11.361

2.  Constitutive protein-DNA interactions on the abscisic acid-responsive element before and after developmental activation of the rab28 gene.

Authors:  P K Busk; J Pujal; A Jessop; V Lumbreras; M Pagès
Journal:  Plant Mol Biol       Date:  1999-11       Impact factor: 4.076

3.  Cell cycle-dependent binding of yeast heat shock factor to nucleosomes.

Authors:  C B Venturi; A M Erkine; D S Gross
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

4.  The developmental activation of the chicken lysozyme locus in transgenic mice requires the interaction of a subset of enhancer elements with the promoter.

Authors:  M C Huber; U Jägle; G Krüger; C Bonifer
Journal:  Nucleic Acids Res       Date:  1997-08-01       Impact factor: 16.971

5.  The polyomavirus enhancer activates chromatin accessibility on integration into the HPRT gene.

Authors:  M Pikaart; J Feng; B Villeponteau
Journal:  Mol Cell Biol       Date:  1992-12       Impact factor: 4.272

6.  Nutritional regulation of nucleosomal structure at the chicken malic enzyme promoter in liver.

Authors:  X J Ma; A G Goodridge
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

7.  Characterization of the human immunoglobulin kappa gene 3' enhancer: functional importance of three motifs that demonstrate B-cell-specific in vivo footprints.

Authors:  J G Judde; E E Max
Journal:  Mol Cell Biol       Date:  1992-11       Impact factor: 4.272

8.  At least three promoters direct expression of the mouse glucocorticoid receptor gene.

Authors:  U Strähle; A Schmidt; G Kelsey; A F Stewart; T J Cole; W Schmid; G Schütz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

9.  Ligand-dependent occupancy of the retinoic acid receptor beta 2 promoter in vivo.

Authors:  A Dey; S Minucci; K Ozato
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

10.  High level activity of the mouse CCAAT/enhancer binding protein (C/EBP alpha) gene promoter involves autoregulation and several ubiquitous transcription factors.

Authors:  C Legraverend; P Antonson; P Flodby; K G Xanthopoulos
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

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