Literature DB >> 34192585

Surprising Twists in Nucleosomal DNA with Implication for Higher-order Folding.

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.
Copyright © 2021 Elsevier Ltd. All rights reserved.

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


  72 in total

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9.  Multiplexing Genetic and Nucleosome Positioning Codes: A Computational Approach.

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2.  emDNA - A Tool for Modeling Protein-decorated DNA Loops and Minicircles at the Base-pair Step Level.

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