Literature DB >> 7460934

Cross-linking of histone H1 in chromatin.

J O Thomas, A J Khabaza.   

Abstract

Arrays of neighbouring histone H1 molecules are present in rat liver chromatin, and can be cross-linked to each other by bisimidoesters. The product, poly(H1), can be extracted from cross-linked chromatin in high yield with 5% perchloric acid and thus distinguished from cross-linked oligomers of the core histones. On analysis in dodecyl sulphate/polyacrylamide gels poly(H1) gives a striking pattern of alternating strong and weak bands which have been shown, by the use of cleavable cross-linked reagents and two-dimensional gel electrophoresis, to arise respectively from H1 homopolymers and H1 polymers linked to the nucleosome core histones. H1-H1 proximities as measured by cross-linking exist both at low ionic strength where the nucleosome filament is extended, and at higher ionic strengths at which it is folded into a 30-nm-diameter fibre, probably in the form of a solenoid, although some additional H1-H1 contacts seem to occur in the folded form. A similar pattern of H1-H1 cross-linking is observed for nucleosome oligomers too short to form a complete turn of a solenoid. The lack of any strong dependence of the H1 cross-linking pattern on ionic strength, and the results for short oligomers, suggest that in a solenoid the major H1-H1 interactions are lateral (i.e. they occur between neighbouring nucleosomes along a turn) although additional vertical contacts (between successive turns) are not excluded. For a short nucleosome oligomer containing n nucleosomes, the number of H1 molecules that may be cross-linked into an array at low ionic strength (approximately 15 mM) is n, consistent with the presence of one H1 per nucleosome. H1-H1 cross-linking occurs only within the chromatin framework; when cross-linking is carried out in 0.5 M NaCl so that H1 is dissociated from chromatin, no poly(H1) is formed. When H1 which has been dissociated in 0.5 M NaCl is allowed to reassociate by gradual lowering of the ionic strength, the poly(H1) is identical with that in native chromatin, suggesting faithful rebinding of H1 molecules. H1-H1 proximities do not seem to be mediated by the presence of bound high-mobility-group non-histone proteins because the poly(H1) pattern persists when cross-linking is carried out at 365 mM ionic strength, when these high-mobility-group proteins are dissociated from chromatin. The H1 cross-linking pattern described here could prove to be a useful assay for the native arrangement of H1 molecules in reconstituted chromatin and for changes in H1-H1 contacts that might result from cell-cycle modifications (e.g phosphorylation) of H1. It may not prove a good assay for higher-order structure because of the relative insensitivity to ionic strength of the poly(H1) pattern as studied here. A detailed analysis will be necessary to determine whether there are any subtle differences in the interactions between H1 molecules in the folded and extended nucleosome filament.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7460934     DOI: 10.1111/j.1432-1033.1980.tb06113.x

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


  15 in total

1.  Sir2p exists in two nucleosome-binding complexes with distinct deacetylase activities.

Authors:  S Ghidelli; D Donze; N Dhillon; R T Kamakaka
Journal:  EMBO J       Date:  2001-08-15       Impact factor: 11.598

2.  Complex of linker histone H5 with the nucleosome and its implications for chromatin packing.

Authors:  Li Fan; Victoria A Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-22       Impact factor: 11.205

3.  Cooperative binding of the globular domains of histones H1 and H5 to DNA.

Authors:  J O Thomas; C Rees; J T Finch
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

4.  The effect of histone H1 and DNA methylation on transcription.

Authors:  C A Johnson; J P Goddard; R L Adams
Journal:  Biochem J       Date:  1995-02-01       Impact factor: 3.857

5.  The involvement of histone H1[0] in chromatin structure.

Authors:  J Roche; J L Girardet; C Gorka; J J Lawrence
Journal:  Nucleic Acids Res       Date:  1985-04-25       Impact factor: 16.971

6.  Cross-linking of histones with dimethyl 3,3'-dithiobispropionimidate. Interference by a one-end reaction modifying histones at lysine amino groups.

Authors:  E Kotthaus; W H Strätling
Journal:  Biochem J       Date:  1984-12-15       Impact factor: 3.857

7.  The layered organization of nucleosomes in 30 nm chromatin fibers.

Authors:  J A Subirana; S Muñoz-Guerra; J Aymamí; M Radermacher; J Frank
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

8.  Coexistence of two chromatin structures in sperm nuclei of the bivalve mollusc Protothaca thaca.

Authors:  C Olivares; M Lila Vera; S Ruíz-Lara
Journal:  Mol Cell Biochem       Date:  1993-08-11       Impact factor: 3.396

9.  Histone H1 and HMG 14/17 are deposited nonrandomly in the nucleus.

Authors:  M Leffak; J P Trempe
Journal:  Nucleic Acids Res       Date:  1985-07-11       Impact factor: 16.971

10.  Chromatin structure of transcriptionally competent and repressed genes.

Authors:  R T Kamakaka; J O Thomas
Journal:  EMBO J       Date:  1990-12       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.