Literature DB >> 2428014

Chicken histone genes retain nuclear matrix association throughout the cell cycle.

S Dalton, H B Younghusband, J R Wells.   

Abstract

The association between histone genes and the nuclear matrix (NM) during periods of high (S-phase) and low (non-S-phase) transcriptional activity has been investigated with synchronized cells from a chicken erythroid cell line (abbreviated ts34). By DNase I and restriction enzyme analysis, these studies reveal that both core and linker histone genes (represented by H2A and H1 genes respectively) are attached to the NM independent of their transcriptional activity during the cell-cycle. The tissue-specific histone gene H5, expressed constitutively, is nuclear matrix (NM)-associated in ts34 cells but is found in the supernatant (S/N) fractions of a non-erythroid T-cell line. Furthermore, we show that DNA sequences necessary for NM-attachment of the H5 gene lie within a 780 base pair region spanning part of the coding and 5' non-translated region. Of the three non-histone genes investigated, beta-actin sequences are expressed and are NM-attached, feather keratin genes are not expressed and predominate in the S/N, and beta-globin genes although not expressed in the ts34 cell line used were found in the NM fraction. In this case the association may be fortuitous or may reflect an early event prior to transcription of globin genes in differentiating erythroid cells. These results generally support the notion that actively transcribed genes are NM-attached, but that attachment per se is not synonymous with transcription.

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Year:  1986        PMID: 2428014      PMCID: PMC311660          DOI: 10.1093/nar/14.16.6507

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  48 in total

1.  Chromosomal subunits in active genes have an altered conformation.

Authors:  H Weintraub; M Groudine
Journal:  Science       Date:  1976-09-03       Impact factor: 47.728

2.  Role of nonhistone proteins in metaphase chromosome structure.

Authors:  K W Adolph; S M Cheng; U K Laemmli
Journal:  Cell       Date:  1977-11       Impact factor: 41.582

3.  The structure of histone-depleted metaphase chromosomes.

Authors:  J R Paulson; U K Laemmli
Journal:  Cell       Date:  1977-11       Impact factor: 41.582

4.  Nucleosome structure III: the structure and transcriptional activity of the chromatin containing the ovalbumin and globin genes in chick oviduct nuclei.

Authors:  M Bellard; F Gannon; P Chambon
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1978

5.  Domains in chromatin structure.

Authors:  T Igó-Kemenes; H G Zachau
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1978

6.  Fractionation of hen oviduct chromatin into transcriptionally active and inactive regions after selective micrococcal nuclease digestion.

Authors:  K S Bloom; J N Anderson
Journal:  Cell       Date:  1978-09       Impact factor: 41.582

7.  Isolation, characterization, and structure of the folded interphase genome of Drosophila melanogaster.

Authors:  C Benyajati; A Worcel
Journal:  Cell       Date:  1976-11       Impact factor: 41.582

8.  Conformational constraints in nuclear DNA.

Authors:  P R Cook; I A Brazell
Journal:  J Cell Sci       Date:  1976-11       Impact factor: 5.285

9.  Rat liver nuclear skeleton and ribonucleoprotein complexes containing HnRNA.

Authors:  T E Miller; C Y Huang; A O Pogo
Journal:  J Cell Biol       Date:  1978-03       Impact factor: 10.539

10.  Heterogeneous nuclear RNA-protein fibers in chromatin-depleted nuclei.

Authors:  R Herman; L Weymouth; S Penman
Journal:  J Cell Biol       Date:  1978-09       Impact factor: 10.539

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  6 in total

1.  Gene positional changes relative to the nuclear substructure correlate with the proliferating status of hepatocytes during liver regeneration.

Authors:  Apolinar Maya-Mendoza; Rolando Hernández-Muñoz; Patricio Gariglio; Armando Aranda-Anzaldo
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

2.  The association of the human epsilon-globin gene with the nuclear matrix: a reconsideration.

Authors:  A J Bartjeliotou; G J Dimitriadis
Journal:  Mol Cell Biochem       Date:  1992-09-22       Impact factor: 3.396

3.  Opposite replication polarities of transcribed and nontranscribed histone H5 genes.

Authors:  J P Trempe; Y I Lindstrom; M Leffak
Journal:  Mol Cell Biol       Date:  1988-04       Impact factor: 4.272

Review 4.  The nuclear matrix--its role in the spatial organization and replication of eukaryotic DNA.

Authors:  H M van der Velden; F Wanka
Journal:  Mol Biol Rep       Date:  1987       Impact factor: 2.316

5.  The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA.

Authors:  J Venema; A van Hoffen; A T Natarajan; A A van Zeeland; L H Mullenders
Journal:  Nucleic Acids Res       Date:  1990-02-11       Impact factor: 16.971

6.  Nuclear matrix associated DNA is preferentially repaired in normal human fibroblasts, exposed to a low dose of ultraviolet light but not in Cockayne's syndrome fibroblasts.

Authors:  L H Mullenders; A C van Kesteren van Leeuwen; A A van Zeeland; A T Natarajan
Journal:  Nucleic Acids Res       Date:  1988-11-25       Impact factor: 16.971

  6 in total

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