| Literature DB >> 34192585 |
Stefjord Todolli1, Robert T Young1, Abigail S Watkins1, Antonio Bu Sha1, John Yager1, Wilma K Olson2.
Abstract
While nucleosomes are dynamic entities that must undergo structural deformations to perform their functions, the general view from available high-resolution structures is a largely static one. Even though numerous examples of twist defects have been documented, the DNA wrapped around the histone core is generally thought to be overtwisted. Analysis of available high-resolution structures from the Protein Data Bank reveals a heterogeneous distribution of twist along the nucleosomal DNA, with clear patterns that are consistent with the literature, and a significant fraction of structures that are undertwisted. The subtle differences in nucleosomal DNA folding, which extend beyond twist, have implications for nucleosome disassembly and modeled higher-order structures. Simulations of oligonucleosome arrays built with undertwisted models behave very differently from those constructed from overtwisted models, in terms of compaction and inter-nucleosome contacts, introducing configurational changes equivalent to those associated with 2-3 base-pair changes in nucleosome spacing. Differences in the nucleosomal DNA pathway, which underlie the way that DNA enters and exits the nucleosome, give rise to different nucleosome-decorated minicircles and affect the topological mix of configurational states.Entities:
Keywords: DNA minicircle; Monte Carlo DNA simulation; nucleosomal twist uptake; nucleosome gaping; oligonucleosome array; undertwisted nucleosome
Mesh:
Substances:
Year: 2021 PMID: 34192585 PMCID: PMC8380738 DOI: 10.1016/j.jmb.2021.167121
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 6.151