Histone Tetrasome Dynamics Affects Chromatin Transcription.
X ShiA S FedulovaE Y KotovaN V MaluchenkoGrigoriy A ArmeevQ ChenC PrasannaA L SivkinaA V FeofanovM P KirpichnikovL NordensköldA K ShaytanV M StuditskyPublished in: bioRxiv : the preprint server for biology (2024)
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 (spFRET) microscopy and NMR 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.
Keyphrases
- energy transfer
- molecular dynamics simulations
- single molecule
- circulating tumor
- dna methylation
- quantum dots
- cell free
- transcription factor
- gene expression
- dna damage
- genome wide
- high resolution
- nucleic acid
- molecular docking
- cell therapy
- circulating tumor cells
- single cell
- high speed
- oxidative stress
- mesenchymal stem cells
- label free
- data analysis