Literature DB >> 7957165

Developmentally regulated expression of linker-histone variants in vertebrates.

S Khochbin1, A P Wolffe.   

Abstract

The identification of histone H1 variants in vertebrates suggests that these proteins may have specialized functions. During embryonic development, a correspondence between the expression of each of the linker-histone variants and the proliferative and transcriptional activity of embryonic cells can be observed. Analysis of the developmentally regulated expression of these variants leads to the subdivision of these variants into distinct classes. This subdivision may also provide insight into the significance of the differential expression of variants and the roles individual linker histones have in chromatin structure and function.

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Year:  1994        PMID: 7957165     DOI: 10.1111/j.1432-1033.1994.00501.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  26 in total

1.  The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts.

Authors:  M H Parseghian; R L Newcomb; S T Winokur; B A Hamkalo
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

2.  Involvement of retinoblastoma protein and HBP1 in histone H1(0) gene expression.

Authors:  C Lemercier; K Duncliffe; I Boibessot; H Zhang; A Verdel; D Angelov; S Khochbin
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

3.  Histone H1 is dispensable for methylation-associated gene silencing in Ascobolus immersus and essential for long life span.

Authors:  J L Barra; L Rhounim; J L Rossignol; G Faugeron
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

4.  The preferential binding of histone H1 to DNA scaffold-associated regions is determined by its C-terminal domain.

Authors:  Alicia Roque; Mary Orrego; Imma Ponte; Pedro Suau
Journal:  Nucleic Acids Res       Date:  2004-11-23       Impact factor: 16.971

5.  Common evolutionary origin and birth-and-death process in the replication-independent histone H1 isoforms from vertebrate and invertebrate genomes.

Authors:  José M Eirín-López; M Fernanda Ruiz; Ana M González-Tizón; Andrés Martínez; Juan Ausió; Lucas Sánchez; Josefina Méndez
Journal:  J Mol Evol       Date:  2005-07-28       Impact factor: 2.395

6.  Nucleosome binding by the polymerase I transactivator upstream binding factor displaces linker histone H1.

Authors:  M Kermekchiev; J L Workman; C S Pikaard
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

7.  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

8.  Histone H1 reduces the frequency of initiation in Xenopus egg extract by limiting the assembly of prereplication complexes on sperm chromatin.

Authors:  Z H Lu; D B Sittman; P Romanowski; G H Leno
Journal:  Mol Biol Cell       Date:  1998-05       Impact factor: 4.138

9.  Histone H1 Is required for proper regulation of pyruvate decarboxylase gene expression in Neurospora crassa.

Authors:  H Diego Folco; Michael Freitag; Ana Ramón; Esteban D Temporini; María E Alvarez; Irene García; Claudio Scazzocchio; Eric U Selker; Alberto L Rosa
Journal:  Eukaryot Cell       Date:  2003-04

10.  S-phase-dependent action of cycloheximide in relieving chromatin-mediated general transcriptional repression.

Authors:  M Cesari; L Héliot; C Meplan; M Pabion; S Khochbin
Journal:  Biochem J       Date:  1998-12-15       Impact factor: 3.857

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