Literature DB >> 8127372

Histone H1 is located in the interior of the chromatin 30-nm filament.

V Graziano1, S E Gerchman, D K Schneider, V Ramakrishnan.   

Abstract

The linker histone H1 binds to the nucleosome and is essential for the organization of nucleosomes into the 30-nm filament of chromatin. It has been implicated in the repression of transcription, and phosphorylation of H1 may be involved in cell-cycle-dependent chromatin condensation and decondensation. A long-standing issue concerns the location of H1 in the chromatin filament. The original solenoidal model proposes that H1 is inside the 30-nm filament, but other models, also helical, suggest a variable or more accessible location for H1. Investigations to determine the location of the linker histone based on its accessibility to antibodies or immobilized proteases under various ionic conditions have yielded conflicting results. Here we use neutron scattering in a direct structural determination to show that H1 is located in the interior of the filament.

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Year:  1994        PMID: 8127372     DOI: 10.1038/368351a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  29 in total

1.  DNase I digestion reveals alternating asymmetrical protection of the nucleosome by the higher order chromatin structure.

Authors:  D Z Staynov
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

2.  Modulation of histone acetyltransferase activity through interaction of epstein-barr nuclear antigen 3C with prothymosin alpha.

Authors:  M A Cotter; E S Robertson
Journal:  Mol Cell Biol       Date:  2000-08       Impact factor: 4.272

3.  EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure.

Authors:  Philip J J Robinson; Louise Fairall; Van A T Huynh; Daniela Rhodes
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-14       Impact factor: 11.205

Review 4.  A variable topology for the 30-nm chromatin fibre.

Authors:  Chenyi Wu; Andrew Bassett; Andrew Travers
Journal:  EMBO Rep       Date:  2007-12       Impact factor: 8.807

5.  Hydrodynamic studies on defined heterochromatin fragments support a 30-nm fiber having six nucleosomes per turn.

Authors:  Rodolfo Ghirlando; Gary Felsenfeld
Journal:  J Mol Biol       Date:  2008-01-03       Impact factor: 5.469

6.  Diffusion-enhanced resonance energy transfer shows that linker-DNA accessibility decreases during salt-induced chromatin condensation.

Authors:  R Labarbe; S Mignon; S Flock; C Houssier
Journal:  J Fluoresc       Date:  1996-06       Impact factor: 2.217

Review 7.  Micromechanical studies of mitotic chromosomes.

Authors:  John F Marko
Journal:  Chromosome Res       Date:  2008       Impact factor: 5.239

8.  Co-operative interactions of oligonucleosomal DNA with the H1e histone variant and its poly(ADP-ribosyl)ated isoform.

Authors:  M D'erme; G Zardo; A Reale; P Caiafa
Journal:  Biochem J       Date:  1996-06-01       Impact factor: 3.857

9.  Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin.

Authors:  J Bednar; R A Horowitz; S A Grigoryev; L M Carruthers; J C Hansen; A J Koster; C L Woodcock
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

10.  The carboxyl terminus of Rtt109 functions in chaperone control of histone acetylation.

Authors:  Ernest Radovani; Matthew Cadorin; Tahireh Shams; Suzan El-Rass; Abdel R Karsou; Hyun-Soo Kim; Christoph F Kurat; Michael-Christopher Keogh; Jack F Greenblatt; Jeffrey S Fillingham
Journal:  Eukaryot Cell       Date:  2013-03-01
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