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Histone tetrasome dynamics affects chromatin transcription

  • Xiangyan Shi
  • , Anastasiia S Fedulova
  • , Elena Y Kotova
  • , Natalya V Maluchenko
  • , Grigoriy A Armeev
  • , Qinming Chen
  • , Chinmayi Prasanna
  • , Anastasia L Sivkina
  • , Alexey V Feofanov
  • , Mikhail P Kirpichnikov
  • , Lars Nordensköld
  • , Alexey K Shaytan
  • , Vasily M Studitsky
  • Shenzhen MSU-BIT University
  • Lomonosov Moscow State University
  • Fox Chase Cancer Center
  • Nanyang Technological University

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

During various DNA-centered processes in the cell nucleus, the minimal structural units of chromatin organization, nucleosomes, are often transiently converted to hexasomes and tetrasomes missing one or both H2A/H2B histone dimers, respectively. However, the structural and functional properties of the subnucleosomes and their impact on biological processes in the nuclei are poorly understood. Here, using biochemical approaches, molecular dynamics simulations, single-particle Förster resonance energy transfer microscopy, and nuclear magnetic resonance spectroscopy, we have shown that, surprisingly, removal of both dimers from a nucleosome results in much higher mobility of both histones and DNA in the tetrasome. Accordingly, DNase I footprinting shows that DNA–histone interactions in tetrasomes are greatly compromised, resulting in formation of a much lower barrier to transcribing RNA polymerase II than nucleosomes. The data suggest that tetrasomes are remarkably dynamic structures and their formation can strongly affect various biological processes.

Original languageEnglish
Article numbergkaf356
JournalNucleic Acids Research
Volume53
Issue number8
DOIs
StatePublished - May 8 2025

Keywords

  • Histones/metabolism
  • Nucleosomes/metabolism
  • Transcription, Genetic
  • Molecular Dynamics Simulation
  • Chromatin/metabolism
  • DNA/metabolism
  • RNA Polymerase II/metabolism
  • Fluorescence Resonance Energy Transfer
  • Animals
  • Humans

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