Literature DB >> 9759497

Alteration of nucleosome structure as a mechanism of transcriptional regulation.

J L Workman1, R E Kingston.   

Abstract

The nucleosome, which is the primary building block of chromatin, is not a static structure: It can adopt alternative conformations. Changes in solution conditions or changes in histone acetylation state cause nucleosomes and nucleosomal arrays to behave with altered biophysical properties. Distinct subpopulations of nucleosomes isolated from cells have chromatographic properties and nuclease sensitivity different from those of bulk nucleosomes. Recently, proteins that were initially identified as necessary for transcriptional regulation have been shown to alter nucleosomal structure. These proteins are found in three types of multiprotein complexes that can acetylate nucleosomes, deacetylate nucleosomes, or alter nucleosome structure in an ATP-dependent manner. The direct modification of nucleosome structure by these complexes is likely to play a central role in appropriate regulation of eukaryotic genes.

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Year:  1998        PMID: 9759497     DOI: 10.1146/annurev.biochem.67.1.545

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  402 in total

1.  Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation.

Authors:  Y Zhang; H H Ng; H Erdjument-Bromage; P Tempst; A Bird; D Reinberg
Journal:  Genes Dev       Date:  1999-08-01       Impact factor: 11.361

2.  Cell cycle-regulated histone acetylation required for expression of the yeast HO gene.

Authors:  J E Krebs; M H Kuo; C D Allis; C L Peterson
Journal:  Genes Dev       Date:  1999-06-01       Impact factor: 11.361

3.  Variegated expression of the endogenous immunoglobulin heavy-chain gene in the absence of the intronic locus control region.

Authors:  D Ronai; M Berru; M J Shulman
Journal:  Mol Cell Biol       Date:  1999-10       Impact factor: 4.272

4.  HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor.

Authors:  A H Wang; N R Bertos; M Vezmar; N Pelletier; M Crosato; H H Heng; J Th'ng; J Han; X J Yang
Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

Review 5.  Chromatin modification by DNA tracking.

Authors:  A Travers
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

6.  Critical role for the histone H4 N terminus in nucleosome remodeling by ISWI.

Authors:  C R Clapier; G Längst; D F Corona; P B Becker; K P Nightingale
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

Review 7.  Regulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins.

Authors:  M Bustin
Journal:  Mol Cell Biol       Date:  1999-08       Impact factor: 4.272

Review 8.  Mechanism and regulation of transcriptional elongation by RNA polymerase II.

Authors:  D Reines; R C Conaway; J W Conaway
Journal:  Curr Opin Cell Biol       Date:  1999-06       Impact factor: 8.382

9.  Crystal structure and mechanism of histone acetylation of the yeast GCN5 transcriptional coactivator.

Authors:  R C Trievel; J R Rojas; D E Sterner; R N Venkataramani; L Wang; J Zhou; C D Allis; S L Berger; R Marmorstein
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

10.  Evolutionary conserved mechanism of transcriptional repression by even-skipped.

Authors:  L M McKay; B Carpenter; S G Roberts
Journal:  Nucleic Acids Res       Date:  1999-08-01       Impact factor: 16.971

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