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STAG2-RAD21 complex: A unidirectional DNA ratchet mechanism in loop extrusion.
- Source :
-
International journal of biological macromolecules [Int J Biol Macromol] 2024 Sep; Vol. 276 (Pt 1), pp. 133822. Date of Electronic Publication: 2024 Jul 14. - Publication Year :
- 2024
-
Abstract
- DNA loop extrusion plays a key role in the regulation of gene expression and the structural arrangement of chromatin. Most existing mechanistic models of loop extrusion depend on some type of ratchet mechanism, which should permit the elongation of loops while preventing their collapse, by enabling DNA to move in only one direction. STAG2 is already known to exert a role as DNA anchor, but the available structural data suggest a possible role in unidirectional DNA motion. In this work, a computational simulation framework was constructed to evaluate whether STAG2 could enforce such unidirectional displacement of a DNA double helix. The results reveal that STAG2 V-shape allows DNA sliding in one direction, but blocks opposite DNA movement via a linear ratchet mechanism. Furthermore, these results suggest that RAD21 binding to STAG2 controls its flexibility by narrowing the opening of its V-shape, which otherwise remains widely open in absence of RAD21. Therefore, in the proposed model, in addition to its already described role as a DNA anchor, the STAG2-RAD21 complex would be part of a ratchet mechanism capable of exerting directional selectivity on DNA sliding during loop extrusion. The identification of the molecular basis of the ratchet mechanism of loop extrusion is a critical step in unraveling new insights into a broad spectrum of chromatin activities and their implications for the mechanisms of chromatin-related diseases.<br />Competing Interests: Declaration of competing interest No competing interest is declared.<br /> (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Protein Binding
Nucleic Acid Conformation
Nuclear Proteins genetics
Nuclear Proteins chemistry
Nuclear Proteins metabolism
Models, Molecular
Humans
Molecular Dynamics Simulation
Chromatin chemistry
Chromatin genetics
Chromatin metabolism
DNA chemistry
DNA genetics
DNA-Binding Proteins chemistry
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Cell Cycle Proteins metabolism
Cell Cycle Proteins genetics
Cell Cycle Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0003
- Volume :
- 276
- Issue :
- Pt 1
- Database :
- MEDLINE
- Journal :
- International journal of biological macromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 39002918
- Full Text :
- https://doi.org/10.1016/j.ijbiomac.2024.133822