Electrostatic mechanism of nucleosomal array folding revealed by computer simulation

Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8180-5. doi: 10.1073/pnas.0408867102. Epub 2005 May 26.

Abstract

Although numerous experiments indicate that the chromatin fiber displays salt-dependent conformations, the associated molecular mechanism remains unclear. Here, we apply an irregular Discrete Surface Charge Optimization (DiSCO) model of the nucleosome with all histone tails incorporated to describe by Monte Carlo simulations salt-dependent rearrangements of a nucleosomal array with 12 nucleosomes. The ensemble of nucleosomal array conformations display salt-dependent condensation in good agreement with hydrodynamic measurements and suggest that the array adopts highly irregular 3D zig-zag conformations at high (physiological) salt concentrations and transitions into the extended "beads-on-a-string" conformation at low salt. Energy analyses indicate that the repulsion among linker DNA leads to this extended form, whereas internucleosome attraction drives the folding at high salt. The balance between these two contributions determines the salt-dependent condensation. Importantly, the internucleosome and linker DNA-nucleosome attractions require histone tails; we find that the H3 tails, in particular, are crucial for stabilizing the moderately folded fiber at physiological monovalent salt.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Computer Simulation*
  • DNA / chemistry
  • DNA / metabolism
  • Histones / chemistry
  • Histones / metabolism
  • Hydrogen Bonding / drug effects
  • Models, Molecular
  • Molecular Conformation*
  • Monte Carlo Method
  • Mutation / genetics
  • Nucleosomes / chemistry*
  • Nucleosomes / metabolism*
  • Probability
  • Salts / pharmacology
  • Static Electricity
  • Temperature
  • Thermodynamics

Substances

  • Histones
  • Nucleosomes
  • Salts
  • DNA