Literature DB >> 1915278

Nucleosomes are positioned with base pair precision adjacent to the alpha 2 operator in Saccharomyces cerevisiae.

M Shimizu1, S Y Roth, C Szent-Gyorgyi, R T Simpson.   

Abstract

Analysis of the chromatin structure of minichromosomes containing the binding site for the yeast alpha 2 repressor protein by indirect end-labeling has previously indicated that nucleosomes are stably positioned over sequences adjacent to the alpha 2 operator in the presence of the repressor. Development of a primer extension assay for nucleosome position now allows a more detailed examination of the location of these nucleosomes relative to the operator sequence, and indicates that nucleosomes are precisely and stably positioned both translationally and rotationally over sequences adjoining the operator. In addition, this assay enables analysis of the chromatin structure of single copy, genomic sequences. Chromatin structures determined for two genes regulated by alpha 2, STE6 and BAR1, are consistent with nucleosomes precisely positioned downstream of the operator sequence, incorporating promoter elements, in alpha cells but not in a-cells. The location of these nucleosomes relative to the operator sequence is highly analogous to that observed in the minichromosome. The stability of the nucleosomes adjacent to the operator together with the precision of their location suggests that they may play a role in repression of a specific gene expression by alpha 2. Further, the primer extension assay allows a comparison of the structure of these positioned nucleosomes formed in vivo to that previously described for core particles reconstituted in vitro.

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Year:  1991        PMID: 1915278      PMCID: PMC453018          DOI: 10.1002/j.1460-2075.1991.tb07854.x

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


  44 in total

Review 1.  Histone function in transcription.

Authors:  M Grunstein
Journal:  Annu Rev Cell Biol       Date:  1990

Review 2.  Nucleosome positioning: occurrence, mechanisms, and functional consequences.

Authors:  R T Simpson
Journal:  Prog Nucleic Acid Res Mol Biol       Date:  1991

Review 3.  A regulatory hierarchy for cell specialization in yeast.

Authors:  I Herskowitz
Journal:  Nature       Date:  1989-12-14       Impact factor: 49.962

4.  Nucleosomes are phased along the mouse beta-major globin gene in erythroid and nonerythroid cells.

Authors:  R Benezra; C R Cantor; R Axel
Journal:  Cell       Date:  1986-03-14       Impact factor: 41.582

5.  Sequences upstream of the STE6 gene required for its expression and regulation by the mating type locus in Saccharomyces cerevisiae.

Authors:  K L Wilson; I Herskowitz
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

6.  Local protein-DNA interactions may determine nucleosome positions on yeast plasmids.

Authors:  F Thoma; R T Simpson
Journal:  Nature       Date:  1985 May 16-22       Impact factor: 49.962

7.  DNA bending and its relation to nucleosome positioning.

Authors:  H R Drew; A A Travers
Journal:  J Mol Biol       Date:  1985-12-20       Impact factor: 5.469

8.  Yeast alpha 2 repressor positions nucleosomes in TRP1/ARS1 chromatin.

Authors:  S Y Roth; A Dean; R T Simpson
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

9.  A repressor (MAT alpha 2 Product) and its operator control expression of a set of cell type specific genes in yeast.

Authors:  A D Johnson; I Herskowitz
Journal:  Cell       Date:  1985-08       Impact factor: 41.582

10.  Removal of positioned nucleosomes from the yeast PHO5 promoter upon PHO5 induction releases additional upstream activating DNA elements.

Authors:  A Almer; H Rudolph; A Hinnen; W Hörz
Journal:  EMBO J       Date:  1986-10       Impact factor: 11.598

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  79 in total

1.  Tup1p represses Mcm1p transcriptional activation and chromatin remodeling of an a-cell-specific gene.

Authors:  I M Gavin; M P Kladde; R T Simpson
Journal:  EMBO J       Date:  2000-11-01       Impact factor: 11.598

2.  DNase I digestion reveals alternating asymmetrical protection of the nucleosome by the higher order chromatin structure.

Authors:  D Z Staynov
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

3.  Histone-dependent association of Tup1-Ssn6 with repressed genes in vivo.

Authors:  Judith K Davie; Robert J Trumbly; Sharon Y R Dent
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

4.  The mapping of nucleosomes and regulatory protein binding sites at the Saccharomyces cerevisiae MFA2 gene: a high resolution approach.

Authors:  Y Teng; S Yu; R Waters
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

5.  Antagonistic remodelling by Swi-Snf and Tup1-Ssn6 of an extensive chromatin region forms the background for FLO1 gene regulation.

Authors:  A B Fleming; S Pennings
Journal:  EMBO J       Date:  2001-09-17       Impact factor: 11.598

6.  Identification of mouse histone deacetylase 1 as a growth factor-inducible gene.

Authors:  S Bartl; J Taplick; G Lagger; H Khier; K Kuchler; C Seiser
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

7.  The organized chromatin domain of the repressed yeast a cell-specific gene STE6 contains two molecules of the corepressor Tup1p per nucleosome.

Authors:  C E Ducker; R T Simpson
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

8.  The Saccharomyces cerevisiae TRT2 tRNAThr gene upstream of STE6 is a barrier to repression in MATalpha cells and exerts a potential tRNA position effect in MATa cells.

Authors:  Tiffany A Simms; Elsy C Miller; Nicolas P Buisson; Nithya Jambunathan; David Donze
Journal:  Nucleic Acids Res       Date:  2004-09-30       Impact factor: 16.971

9.  Corepressor-directed preacetylation of histone H3 in promoter chromatin primes rapid transcriptional switching of cell-type-specific genes in yeast.

Authors:  Alec M Desimone; Jeffrey D Laney
Journal:  Mol Cell Biol       Date:  2010-05-03       Impact factor: 4.272

10.  Nucleosome positioning, nucleosome spacing and the nucleosome code.

Authors:  David J Clark
Journal:  J Biomol Struct Dyn       Date:  2010-06
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