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DNA i-motif formation at neutral pH is driven by kinetic partitioning
Cytosine-rich DNA regions can form four-stranded structures based on hemi-protonated C.C(+) pairs, called i-motifs (iMs). Using CD, UV absorption, NMR spectroscopy, and DSC calorimetry, we show that model (C(n)T(3))(3)C(n) (Cn) sequences adopt iM under neutral or slightly alkaline conditions for n &...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085675/ https://www.ncbi.nlm.nih.gov/pubmed/36912102 http://dx.doi.org/10.1093/nar/gkad119 |
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author | Školáková, Petra Gajarský, Martin Palacký, Jan Šubert, Denis Renčiuk, Daniel Trantírek, Lukáš Mergny, Jean-Louis Vorlíčková, Michaela |
author_facet | Školáková, Petra Gajarský, Martin Palacký, Jan Šubert, Denis Renčiuk, Daniel Trantírek, Lukáš Mergny, Jean-Louis Vorlíčková, Michaela |
author_sort | Školáková, Petra |
collection | PubMed |
description | Cytosine-rich DNA regions can form four-stranded structures based on hemi-protonated C.C(+) pairs, called i-motifs (iMs). Using CD, UV absorption, NMR spectroscopy, and DSC calorimetry, we show that model (C(n)T(3))(3)C(n) (Cn) sequences adopt iM under neutral or slightly alkaline conditions for n > 3. However, the iMs are formed with long-lasting kinetics under these conditions and melt with significant hysteresis. Sequences with n > 6 melt in two or more separate steps, indicating the presence of different iM species, the proportion of which is dependent on temperature and incubation time. At ambient temperature, kinetically favored iMs of low stability are formed, most likely consisting of short C.C(+) blocks. These species act as kinetic traps and prevent the assembly of thermodynamically favored, fully C.C(+) paired iMs. A higher temperature is necessary to unfold the kinetic forms and enable their substitution by a slowly developing thermodynamic structure. This complicated kinetic partitioning process considerably slows down iM folding, making it much slower than the timeframes of biological reactions and, therefore, unlikely to have any biological relevance. Our data suggest kinetically driven iM species as more likely to be biologically relevant than thermodynamically most stable iM forms. |
format | Online Article Text |
id | pubmed-10085675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100856752023-04-11 DNA i-motif formation at neutral pH is driven by kinetic partitioning Školáková, Petra Gajarský, Martin Palacký, Jan Šubert, Denis Renčiuk, Daniel Trantírek, Lukáš Mergny, Jean-Louis Vorlíčková, Michaela Nucleic Acids Res Structural Biology Cytosine-rich DNA regions can form four-stranded structures based on hemi-protonated C.C(+) pairs, called i-motifs (iMs). Using CD, UV absorption, NMR spectroscopy, and DSC calorimetry, we show that model (C(n)T(3))(3)C(n) (Cn) sequences adopt iM under neutral or slightly alkaline conditions for n > 3. However, the iMs are formed with long-lasting kinetics under these conditions and melt with significant hysteresis. Sequences with n > 6 melt in two or more separate steps, indicating the presence of different iM species, the proportion of which is dependent on temperature and incubation time. At ambient temperature, kinetically favored iMs of low stability are formed, most likely consisting of short C.C(+) blocks. These species act as kinetic traps and prevent the assembly of thermodynamically favored, fully C.C(+) paired iMs. A higher temperature is necessary to unfold the kinetic forms and enable their substitution by a slowly developing thermodynamic structure. This complicated kinetic partitioning process considerably slows down iM folding, making it much slower than the timeframes of biological reactions and, therefore, unlikely to have any biological relevance. Our data suggest kinetically driven iM species as more likely to be biologically relevant than thermodynamically most stable iM forms. Oxford University Press 2023-03-13 /pmc/articles/PMC10085675/ /pubmed/36912102 http://dx.doi.org/10.1093/nar/gkad119 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Structural Biology Školáková, Petra Gajarský, Martin Palacký, Jan Šubert, Denis Renčiuk, Daniel Trantírek, Lukáš Mergny, Jean-Louis Vorlíčková, Michaela DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title | DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title_full | DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title_fullStr | DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title_full_unstemmed | DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title_short | DNA i-motif formation at neutral pH is driven by kinetic partitioning |
title_sort | dna i-motif formation at neutral ph is driven by kinetic partitioning |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085675/ https://www.ncbi.nlm.nih.gov/pubmed/36912102 http://dx.doi.org/10.1093/nar/gkad119 |
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