Literature DB >> 3048335

The production of tissue-specific histone complements during development.

R W Lennox1, L H Cohen.   

Abstract

At least two mechanisms generate tissue differences in the histone subtype composition during development: subtype dilution and subtype replacement. Subtype dilution, which occurs when cells continue dividing after having ceased to synthesize one more histone subtypes, allows the elimination of stable subtypes. It is the major mechanism generating cell differences in histone composition in sea urchin embryogenesis. Subtype replacement has been observed in mammalian tissues, both in the intact animal and in cultured cells. It is most evident in nondividing cells but occurs to some extent in dividing cells as well. Examples of the two mechanisms are presented and their possible biological significance, as well as that of the differences they produce, is discussed.

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Year:  1988        PMID: 3048335     DOI: 10.1139/o88-073

Source DB:  PubMed          Journal:  Biochem Cell Biol        ISSN: 0829-8211            Impact factor:   3.626


  11 in total

1.  Histone mRNAs do not accumulate during S phase of either mitotic or endoreduplicative cycles in the chordate Oikopleura dioica.

Authors:  Mariacristina Chioda; Fabio Spada; Ragnhild Eskeland; Eric M Thompson
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

2.  Polymorphism of histone H1 in goose erythrocytes.

Authors:  J Pałyga
Journal:  Biochem Genet       Date:  1990-08       Impact factor: 1.890

Review 3.  Relationship of eukaryotic DNA replication to committed gene expression: general theory for gene control.

Authors:  L P Villarreal
Journal:  Microbiol Rev       Date:  1991-09

4.  Organization and roles of nucleosomes at mouse meiotic recombination hotspots.

Authors:  Irina V Getun; Zhen K Wu; Philippe R J Bois
Journal:  Nucleus       Date:  2012-05-01       Impact factor: 4.197

5.  Differential effect of H1 variant overproduction on gene expression is due to differences in the central globular domain.

Authors:  D T Brown; A Gunjan; B T Alexander; D B Sittman
Journal:  Nucleic Acids Res       Date:  1997-12-15       Impact factor: 16.971

6.  Differential effect of H1 variant overexpression on cell cycle progression and gene expression.

Authors:  D T Brown; B T Alexander; D B Sittman
Journal:  Nucleic Acids Res       Date:  1996-02-01       Impact factor: 16.971

7.  Site-specifically phosphorylated forms of H1.5 and H1.2 localized at distinct regions of the nucleus are related to different processes during the cell cycle.

Authors:  Heribert Talasz; Bettina Sarg; Herbert H Lindner
Journal:  Chromosoma       Date:  2009-07-16       Impact factor: 4.316

8.  Auxin and epigenetic regulation of SKP2B, an F-box that represses lateral root formation.

Authors:  Concepción Manzano; Elena Ramirez-Parra; Ilda Casimiro; Sofía Otero; Bénédicte Desvoyes; Bert De Rybel; Tom Beeckman; Pedro Casero; Crisanto Gutierrez; Juan C Del Pozo
Journal:  Plant Physiol       Date:  2012-07-26       Impact factor: 8.340

9.  HILS1 is a spermatid-specific linker histone H1-like protein implicated in chromatin remodeling during mammalian spermiogenesis.

Authors:  Wei Yan; Lang Ma; Kathleen H Burns; Martin M Matzuk
Journal:  Proc Natl Acad Sci U S A       Date:  2003-08-14       Impact factor: 11.205

10.  Characterization and chromatin distribution of the H1 histones and high-mobility-group non-histone chromosomal proteins of trout liver and hepatocellular carcinoma.

Authors:  J R Davie; G P Delcuve
Journal:  Biochem J       Date:  1991-12-01       Impact factor: 3.857

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