Literature DB >> 8575881

The nuclear matrix and the regulation of chromatin organization and function.

J R Davie1.   

Abstract

Nuclear DNA is organized into loop domains, with the base of the loop being bound to the nuclear matrix. Loops with transcriptionally active and/or potentially active genes have a DNase I-sensitive chromatin structure, while repressed chromatin loops have a condensed configuration that is essentially invisible to the transcription machinery. Core histone acetylation and torsional stress appear to be responsible for the generation and/or maintenance of the open potentially active chromatin loops. The transcriptionally active region of the loop makes several dynamic attachments with the nuclear matrix and is associated with core histones that are dynamically acetylated. Histone acetyltransferase and deacetylase, which catalyze this rapid acetylation and deacetylation, are bound to the nuclear matrix. Several transcription factors are components of the nuclear matrix. Histone acetyltransferase, deacetylase, and transcription factors may contribute to the dynamic attachment of the active chromatin domains with the nuclear matrix at sites of ongoing transcription.

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Year:  1995        PMID: 8575881     DOI: 10.1016/s0074-7696(08)61232-2

Source DB:  PubMed          Journal:  Int Rev Cytol        ISSN: 0074-7696


  16 in total

1.  Flanking nuclear matrix attachment regions synergize with the T cell receptor delta enhancer to promote V(D)J recombination.

Authors:  X P Zhong; J Carabaña; M S Krangel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

2.  The analysis of the poly(ADPR) polymerase mode of action in rat testis nuclear fractions defines a specific poly(ADP-ribosyl)ation system associated with the nuclear matrix.

Authors:  P Quesada; F Tramontano; M R Faraone-Mennella; B Farina
Journal:  Mol Cell Biochem       Date:  2000-02       Impact factor: 3.396

3.  The matrix attachment region-binding protein SATB1 participates in negative regulation of tissue-specific gene expression.

Authors:  J Liu; D Bramblett; Q Zhu; M Lozano; R Kobayashi; S R Ross; J P Dudley
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

4.  The effects of histone acetylation on estrogen responsiveness in MCF-7 cells.

Authors:  M F Ruh; S Tian; L K Cox; T S Ruh
Journal:  Endocrine       Date:  1999-10       Impact factor: 3.633

Review 5.  Extracellular matrix, nuclear and chromatin structure, and gene expression in normal tissues and malignant tumors: a work in progress.

Authors:  Virginia A Spencer; Ren Xu; Mina J Bissell
Journal:  Adv Cancer Res       Date:  2007       Impact factor: 6.242

6.  Structural requirements and dynamics of mitosin-kinetochore interaction in M phase.

Authors:  X Zhu
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

7.  Higher order chromatin structures in maize and Arabidopsis.

Authors:  A L Paul; R J Ferl
Journal:  Plant Cell       Date:  1998-08       Impact factor: 11.277

Review 8.  Nuclear matrix, dynamic histone acetylation and transcriptionally active chromatin.

Authors:  J R Davie
Journal:  Mol Biol Rep       Date:  1997-08       Impact factor: 2.316

9.  Identifying Nuclear Matrix-Attached DNA Across the Genome.

Authors:  Jason R Dobson; Deli Hong; A Rasim Barutcu; Hai Wu; Anthony N Imbalzano; Jane B Lian; Janet L Stein; Andre J van Wijnen; Jeffrey A Nickerson; Gary S Stein
Journal:  J Cell Physiol       Date:  2017-01-05       Impact factor: 6.384

10.  Vertebrate Protein CTCF and its Multiple Roles in a Large-Scale Regulation of Genome Activity.

Authors:  L G Nikolaev; S B Akopov; D A Didych; E D Sverdlov
Journal:  Curr Genomics       Date:  2009-08       Impact factor: 2.236

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