Literature DB >> 1312335

Reversible histone modifications and the chromosome cell cycle.

E M Bradbury1.   

Abstract

During the eukaryotic cell cycle, chromosomes undergo large structural transitions and spatial rearrangements that are associated with the major cell functions of genome replication, transcription and chromosome condensation to metaphase chromosomes. Eukaryotic cells have evolved cell cycle dependent processes that modulate histone:DNA interactions in chromosomes. These are; i) acetylations of lysines; ii) phosphorylations of serines and threonines and iii) ubiquitinations of lysines. All of these reversible modifications are contained in the well-defined very basic N- and C-terminal domains of histones. Acetylations and phosphorylations markedly affect the charge densities of these domains whereas ubiquitination adds a bulky globular protein, ubiquitin, to lysines in the C-terminal tails of H2A and H2B. Histone acetylations are strictly associated with genome replication and transcription; histone H1 and H3 phosphorylations correlate with the process of chromosome condensation. The subunits of histone H1 kinase have now been shown to be cyclins and the p34CDC2 kinase product of the cell cycle control gene CDC2. It is probable that all of the processes that control chromosome structure:function relationships are also involved in the control of the cell cycle.

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Year:  1992        PMID: 1312335     DOI: 10.1002/bies.950140103

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  107 in total

1.  Core histone N-termini play an essential role in mitotic chromosome condensation.

Authors:  A E de la Barre; V Gerson; S Gout; M Creaven; C D Allis; S Dimitrov
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

2.  Efficiency of expression of transfected genes depends on the cell cycle.

Authors:  S Marenzi; R L Adams; G Zardo; L Lenti; A Reale; P Caiafa
Journal:  Mol Biol Rep       Date:  1999-12       Impact factor: 2.316

3.  A mutant deubiquitinating enzyme (Ubp-M) associates with mitotic chromosomes and blocks cell division.

Authors:  S Y Cai; R W Babbitt; V T Marchesi
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

4.  Stable remodeling of tailless nucleosomes by the human SWI-SNF complex.

Authors:  J R Guyon; G J Narlikar; S Sif; R E Kingston
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

5.  Gadd45, a p53-responsive stress protein, modifies DNA accessibility on damaged chromatin.

Authors:  F Carrier; P T Georgel; P Pourquier; M Blake; H U Kontny; M J Antinore; M Gariboldi; T G Myers; J N Weinstein; Y Pommier; A J Fornace
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

Review 6.  Chromatin modification and disease.

Authors:  C A Johnson
Journal:  J Med Genet       Date:  2000-12       Impact factor: 6.318

7.  The N-terminus of histone H2B, but not that of histone H3 or its phosphorylation, is essential for chromosome condensation.

Authors:  A E de la Barre; D Angelov; A Molla; S Dimitrov
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

Review 8.  Duality in bromodomain-containing protein complexes.

Authors:  G V Denis
Journal:  Front Biosci       Date:  2001-08-01

9.  Histone H3 phosphorylation of mammalian chromosomes.

Authors:  A Garcia-Orad; P G Vargas; B K Vig
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

Review 10.  Degradation or maintenance: actions of the ubiquitin system on eukaryotic chromatin.

Authors:  Helle D Ulrich
Journal:  Eukaryot Cell       Date:  2002-02
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