Structure and Dynamics of a 197 bp Nucleosome in Complex with Linker Histone H1

Mol Cell. 2017 May 4;66(3):384-397.e8. doi: 10.1016/j.molcel.2017.04.012.

Abstract

Linker histones associate with nucleosomes to promote the formation of higher-order chromatin structure, but the underlying molecular details are unclear. We investigated the structure of a 197 bp nucleosome bearing symmetric 25 bp linker DNA arms in complex with vertebrate linker histone H1. We determined electron cryo-microscopy (cryo-EM) and crystal structures of unbound and H1-bound nucleosomes and validated these structures by site-directed protein cross-linking and hydroxyl radical footprinting experiments. Histone H1 shifts the conformational landscape of the nucleosome by drawing the two linkers together and reducing their flexibility. The H1 C-terminal domain (CTD) localizes primarily to a single linker, while the H1 globular domain contacts the nucleosome dyad and both linkers, associating more closely with the CTD-distal linker. These findings reveal that H1 imparts a strong degree of asymmetry to the nucleosome, which is likely to influence the assembly and architecture of higher-order structures.

Keywords: X-ray crystallography; chromatin; cryo-EM; histone H1; hydroxyl radical footprinting; linker histone; nucleosome; protein-DNA crosslinking.

MeSH terms

  • Animals
  • Base Pairing
  • Binding Sites
  • Chromatin / chemistry
  • Chromatin / genetics
  • Chromatin / metabolism*
  • Chromatin / ultrastructure
  • Chromatin Assembly and Disassembly*
  • Cryoelectron Microscopy
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism*
  • Histones / chemistry
  • Histones / metabolism*
  • Humans
  • Models, Molecular
  • Nucleosomes / chemistry
  • Nucleosomes / genetics
  • Nucleosomes / metabolism*
  • Nucleosomes / ultrastructure
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Structure-Activity Relationship
  • Time Factors
  • Xenopus laevis / genetics
  • Xenopus laevis / metabolism

Substances

  • Chromatin
  • Histones
  • Nucleosomes
  • DNA