Literature DB >> 12547190

Sequence-dependent nucleosome structural and dynamic polymorphism. Potential involvement of histone H2B N-terminal tail proximal domain.

Andrei Sivolob1, Christophe Lavelle, Ariel Prunell.   

Abstract

Relaxation of nucleosomes on an homologous series (pBR) of ca 350-370 bp DNA minicircles originating from plasmid pBR322 was recently used as a tool to study their structure and dynamics. These nucleosomes thermally fluctuated between three distinct DNA conformations within a histone N-terminal tail-modulated equilibrium: one conformation was canonical, with 1.75 turn wrapping and negatively crossed entering and exiting DNAs; another was also "closed", but with these DNAs positively crossed; and the third was "open", with a lower than 1.5 turn wrapping and uncrossed DNAs. In this work, a new minicircle series (5S) of similar size was used, which contained the 5S nucleosome positioning sequence. Results showed that DNA in pBR nucleosomes was untwisted by approximately 0.2 turn relative to 5S nucleosomes, which DNase I footprinting confirmed in revealing a approximately 1 bp untwisting at each of the two dyad-distal sites where H2B N-terminal tails pass between the two gyres. In contrast, both nucleosomes showed untwistings at the dyad-proximal sites, i.e. on the other gyre, which were also observed in the high-resolution crystal structure. 5S nucleosomes also differ with respect to their dynamics: they hardly accessed the positively crossed conformation, but had an easier access to the negatively crossed conformation. Simulation showed that such reverse effects on the conformational free energies could be simply achieved by slightly altering the trajectories of entering and exiting DNAs. We propose that this is accomplished by H2B tail untwisting at the distal sites through action at a distance ( approximately 20 bp) on H3-tail interactions with the small groove at the nucleosome entry-exit. These results may help to gain a first glimpse into the two perhaps most intriguing features of the high-resolution structure: the alignment of the grooves on the two gyres and the passage of H2B and H3 N-terminal tails between them.

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Year:  2003        PMID: 12547190     DOI: 10.1016/s0022-2836(02)01372-4

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  13 in total

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2.  Chromatin fiber functional organization: some plausible models.

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3.  H2A and H2B tails are essential to properly reconstitute nucleosome core particles.

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4.  On the topology of chromatin fibres.

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Journal:  Interface Focus       Date:  2012-02-01       Impact factor: 3.906

5.  DNA topology in chromosomes: a quantitative survey and its physiological implications.

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6.  A cassette of basic amino acids in histone H2B regulates nucleosome dynamics and access to DNA damage.

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Journal:  J Biol Chem       Date:  2018-03-27       Impact factor: 5.157

Review 7.  Chromatin fiber dynamics under tension and torsion.

Authors:  Christophe Lavelle; Jean-Marc Victor; Jordanka Zlatanova
Journal:  Int J Mol Sci       Date:  2010-04-12       Impact factor: 5.923

8.  Surprising Twists in Nucleosomal DNA with Implication for Higher-order Folding.

Authors:  Stefjord Todolli; Robert T Young; Abigail S Watkins; Antonio Bu Sha; John Yager; Wilma K Olson
Journal:  J Mol Biol       Date:  2021-06-28       Impact factor: 6.151

9.  A cassette of N-terminal amino acids of histone H2B are required for efficient cell survival, DNA repair and Swi/Snf binding in UV irradiated yeast.

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Journal:  Nucleic Acids Res       Date:  2009-12-09       Impact factor: 16.971

10.  Rad51 polymerization reveals a new chromatin remodeling mechanism.

Authors:  Pauline Dupaigne; Christophe Lavelle; Anthony Justome; Sophie Lafosse; Gilles Mirambeau; Marc Lipinski; Olivier Piétrement; Eric Le Cam
Journal:  PLoS One       Date:  2008-11-04       Impact factor: 3.240

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