Nucleosome composition regulates the histone H3 tail conformational ensemble and accessibility

Author:

Morrison Emma A12ORCID,Baweja Lokesh34,Poirier Michael G5ORCID,Wereszczynski Jeff34ORCID,Musselman Catherine A16ORCID

Affiliation:

1. Department of Biochemistry, Carver College of Medicine, University of Iowa, Iowa City, IA, USA

2. Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA

3. Department of Physics, Illinois Institute of Technology, Chicago, IL, USA

4. Center for Molecular Study of Condensed Soft Matter, Illinois Institute of Technology, Chicago, IL, USA

5. Department of Physics, Biophysics Graduate Program, Ohio State Biochemistry Graduate Program, and Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH, USA

6. Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA

Abstract

Abstract Hexasomes and tetrasomes are intermediates in nucleosome assembly and disassembly. Their formation is promoted by histone chaperones, ATP-dependent remodelers, and RNA polymerase II. In addition, hexasomes are maintained in transcribed genes and could be an important regulatory factor. While nucleosome composition has been shown to affect the structure and accessibility of DNA, its influence on histone tails is largely unknown. Here, we investigate the conformational dynamics of the H3 tail in the hexasome and tetrasome. Using a combination of NMR spectroscopy, MD simulations, and trypsin proteolysis, we find that the conformational ensemble of the H3 tail is regulated by nucleosome composition. As has been found for the nucleosome, the H3 tails bind robustly to DNA within the hexasome and tetrasome, but upon loss of the H2A/H2B dimer, we determined that the adjacent H3 tail has an altered conformational ensemble, increase in dynamics, and increase in accessibility. Similar to observations of DNA dynamics, this is seen to be asymmetric in the hexasome. Our results indicate that nucleosome composition has the potential to regulate chromatin signaling and ultimately help shape the chromatin landscape.

Funder

NSF

NIH

Medical College of Wisconsin

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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