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Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes
Guanine-rich DNA sequences tend to form four-stranded G-quadruplex structures. Characteristic glycosidic conformational patterns along the G-strands, such as the 5′-syn-anti-syn-anti pattern observed with the Oxytricha nova telomeric G-quadruplexes, have been well documented. However, an explanation...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105399/ https://www.ncbi.nlm.nih.gov/pubmed/21296760 http://dx.doi.org/10.1093/nar/gkr031 |
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author | Cang, Xiaohui Šponer, Jiří Cheatham, Thomas E. |
author_facet | Cang, Xiaohui Šponer, Jiří Cheatham, Thomas E. |
author_sort | Cang, Xiaohui |
collection | PubMed |
description | Guanine-rich DNA sequences tend to form four-stranded G-quadruplex structures. Characteristic glycosidic conformational patterns along the G-strands, such as the 5′-syn-anti-syn-anti pattern observed with the Oxytricha nova telomeric G-quadruplexes, have been well documented. However, an explanation for these featured glycosidic patterns has not emerged. This work presents MD simulation and free energetic analyses for simplified two-quartet [d(GG)](4) models and suggests that the four base pair step patterns show quite different relative stabilities: syn-anti > anti-anti > anti-syn > syn-syn. This suggests the following rule: when folding, anti-parallel G-quadruplexes tend to maximize the number of syn-anti steps and avoid the unfavorable anti-syn and syn-syn steps. This rule is consistent with most of the anti-parallel G-quadruplex structures in the Protein Databank (PDB). Structural polymorphisms of G-quadruplexes relate to these glycosidic conformational patterns and the lengths of the G-tracts. The folding topologies of G2- and G4-tracts are not very polymorphic because each strand tends to populate the stable syn-anti repeat. G3-tracts, on the other hand, cannot present this repeating pattern on each G-tract. This leads to smaller energy differences between different geometries and helps explain the extreme structural polymorphism of the human telomeric G-quadruplexes. |
format | Text |
id | pubmed-3105399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31053992011-06-01 Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes Cang, Xiaohui Šponer, Jiří Cheatham, Thomas E. Nucleic Acids Res Structural Biology Guanine-rich DNA sequences tend to form four-stranded G-quadruplex structures. Characteristic glycosidic conformational patterns along the G-strands, such as the 5′-syn-anti-syn-anti pattern observed with the Oxytricha nova telomeric G-quadruplexes, have been well documented. However, an explanation for these featured glycosidic patterns has not emerged. This work presents MD simulation and free energetic analyses for simplified two-quartet [d(GG)](4) models and suggests that the four base pair step patterns show quite different relative stabilities: syn-anti > anti-anti > anti-syn > syn-syn. This suggests the following rule: when folding, anti-parallel G-quadruplexes tend to maximize the number of syn-anti steps and avoid the unfavorable anti-syn and syn-syn steps. This rule is consistent with most of the anti-parallel G-quadruplex structures in the Protein Databank (PDB). Structural polymorphisms of G-quadruplexes relate to these glycosidic conformational patterns and the lengths of the G-tracts. The folding topologies of G2- and G4-tracts are not very polymorphic because each strand tends to populate the stable syn-anti repeat. G3-tracts, on the other hand, cannot present this repeating pattern on each G-tract. This leads to smaller energy differences between different geometries and helps explain the extreme structural polymorphism of the human telomeric G-quadruplexes. Oxford University Press 2011-05 2011-02-03 /pmc/articles/PMC3105399/ /pubmed/21296760 http://dx.doi.org/10.1093/nar/gkr031 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Cang, Xiaohui Šponer, Jiří Cheatham, Thomas E. Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title | Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title_full | Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title_fullStr | Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title_full_unstemmed | Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title_short | Explaining the varied glycosidic conformational, G-tract length and sequence preferences for anti-parallel G-quadruplexes |
title_sort | explaining the varied glycosidic conformational, g-tract length and sequence preferences for anti-parallel g-quadruplexes |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105399/ https://www.ncbi.nlm.nih.gov/pubmed/21296760 http://dx.doi.org/10.1093/nar/gkr031 |
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