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Torque modulates nucleosome stability and facilitates H2A/H2B dimer loss
Maxim Y Sheinin1, Ming Li, Mohammad Soltani
1Department of Physics-Laboratory of Atomic and Solid State Physics, Cornell University, Ithaca, New York 14853, USA.
Nature Communications
|October 12, 2013
Summary
DNA supercoiling and nucleosome chirality are crucial for cellular processes. This study reveals that torque primarily affects histone dimer loss, not DNA unwrapping, impacting histone exchange during transcription and replication.
Area of Science:
- Molecular Biology
- Biophysics
- Genetics
Background:
- Nucleosomes, the fundamental units of chromatin, exhibit a left-handed chirality due to DNA wrapping around core histones.
- This DNA superhelix chirality is hypothesized to be functionally significant in DNA supercoiling-dependent cellular processes like transcription and replication.
- The precise impact of torsional stress on nucleosome structure and stability remains largely uncharacterized.
Purpose of the Study:
- To investigate the effects of tension and torque on the structural behavior and stability of single nucleosomes.
- To elucidate the role of torsion in nucleosome unwrapping and histone dissociation.
Main Methods:
- Utilized the angular optical trapping technique to apply controlled tension and torque to single nucleosomes.
- Studied nucleosome behavior on the high-affinity 601-DNA positioning sequence.
Main Results:
- Torque exerted a moderate influence on the unwrapping of DNA from the nucleosome.
- Positive torque induced a significant dissociation of H2A/H2B histone dimers from the nucleosome.
- (H3/H4)₂ tetramers demonstrated high retention efficiency, independent of applied torsion.
Conclusions:
- Torsional stress has a differential impact on nucleosome components, primarily affecting histone dimer stability.
- These findings suggest a regulatory mechanism where torque influences histone exchange, potentially modulating chromatin dynamics during DNA replication and transcription.
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