Effect of force on mononucleosomal dynamics
- 24 October 2006
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 103 (43) , 15871-15876
- https://doi.org/10.1073/pnas.0607526103
Abstract
Using single-molecule optical-trapping techniques, we examined the force-induced dynamic behavior of a single nucleosome core particle. Our experiments using the DNA construct containing the 601 nucleosome-positioning sequence revealed that the nucleosome unravels in at least two major stages. The first stage, which we attributed to the unraveling of the first DNA wrap around the histone octamer, could be mechanically induced in a reversible manner, and when kept at constant force within a critical force range, exhibited two-state hopping behavior. From the hopping data, we determined the force-dependent equilibrium constant and rates for opening/closing of the outer wrap. Our investigation of the second unraveling event at various loading rates, which we attributed to the inner DNA wrap, revealed that this unraveling event cannot be described as a simple two-state process. We also looked at the behavior of the mononucleosome in a high-salt buffer, which revealed that the outer DNA wrap is more sensitive to changes in the ionic environment than the inner DNA wrap. These findings are needed to understand the energetics of nucleosome remodeling.Keywords
This publication has 30 references indexed in Scilit:
- Forced Unraveling of Nucleosomes Assembled on Heterogeneous DNA Using Core Histones, NAP-1, and ACFJournal of Molecular Biology, 2005
- Specific Contributions of Histone Tails and their Acetylation to the Mechanical Stability of NucleosomesJournal of Molecular Biology, 2005
- Rapid spontaneous accessibility of nucleosomal DNANature Structural & Molecular Biology, 2004
- Mechanical Processes in BiochemistryAnnual Review of Biochemistry, 2004
- Using mechanical force to probe the mechanism of pausing and arrest during continuous elongation by Escherichia coli RNA polymeraseProceedings of the National Academy of Sciences, 2002
- Single-Molecule Study of Transcriptional Pausing and Arrest by E. coli RNA PolymeraseScience, 2000
- Sequence and position-dependence of the equilibrium accessibility of nucleosomal DNA target sites 1 1Edited by T. RichmondJournal of Molecular Biology, 2000
- New DNA sequence rules for high affinity binding to histone octamer and sequence-directed nucleosome positioningJournal of Molecular Biology, 1998
- Effects of DNA sequence and histone-histone interactions on nucleosome placementJournal of Molecular Biology, 1990
- Salt-induced release of DNA from nucleosome core particlesBiochemistry, 1989