Literature DB >> 16603492

Flexible histone tails in a new mesoscopic oligonucleosome model.

Gaurav Arya1, Qing Zhang, Tamar Schlick.   

Abstract

We describe a new mesoscopic model of oligonucleosomes that incorporates flexible histone tails. The nucleosome cores are modeled using the discrete surface-charge optimization model, which treats the nucleosome as an electrostatic surface represented by hundreds of point charges; the linker DNAs are treated using a discrete elastic chain model; and the histone tails are modeled using a bead/chain hydrodynamic approach as chains of connected beads where each bead represents five protein residues. Appropriate charges and force fields are assigned to each histone chain so as to reproduce the electrostatic potential, structure, and dynamics of the corresponding atomistic histone tails at different salt conditions. The dynamics of resulting oligonucleosomes at different sizes and varying salt concentrations are simulated by Brownian dynamics with complete hydrodynamic interactions. The analyses demonstrate that the new mesoscopic model reproduces experimental results better than its predecessors, which modeled histone tails as rigid entities. In particular, our model with flexible histone tails: correctly accounts for salt-dependent conformational changes in the histone tails; yields the experimentally obtained values of histone-tail mediated core/core attraction energies; and considers the partial shielding of electrostatic repulsion between DNA linkers as a result of the spatial distribution of histone tails. These effects are crucial for regulating chromatin structure but are absent or improperly treated in models with rigid histone tails. The development of this model of oligonucleosomes thus opens new avenues for studying the role of histone tails and their variants in mediating gene expression through modulation of chromatin structure.

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Year:  2006        PMID: 16603492      PMCID: PMC1479056          DOI: 10.1529/biophysj.106.083006

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  43 in total

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4.  Modeling salt-mediated electrostatics of macromolecules: the discrete surface charge optimization algorithm and its application to the nucleosome.

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  49 in total

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2.  The effect of linker histone's nucleosome binding affinity on chromatin unfolding mechanisms.

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5.  Twist propagation in dinucleosome arrays.

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Journal:  Biophys J       Date:  2010-11-17       Impact factor: 4.033

6.  Local geometry and elasticity in compact chromatin structure.

Authors:  Elena F Koslover; Colin J Fuller; Aaron F Straight; Andrew J Spakowitz
Journal:  Biophys J       Date:  2010-12-15       Impact factor: 4.033

7.  H3 and H4 histone tails play a central role in the interactions of recombinant NCPs.

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8.  Role of histone tails in chromatin folding revealed by a mesoscopic oligonucleosome model.

Authors:  Gaurav Arya; Tamar Schlick
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-23       Impact factor: 11.205

9.  Bridging chromatin structure and function over a range of experimental spatial and temporal scales by molecular modeling.

Authors:  Stephanie Portillo-Ledesma; Tamar Schlick
Journal:  Wiley Interdiscip Rev Comput Mol Sci       Date:  2019-08-06

10.  A tale of tails: how histone tails mediate chromatin compaction in different salt and linker histone environments.

Authors:  Gaurav Arya; Tamar Schlick
Journal:  J Phys Chem A       Date:  2009-04-23       Impact factor: 2.781

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