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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 &...

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Autores principales: Školáková, Petra, Gajarský, Martin, Palacký, Jan, Šubert, Denis, Renčiuk, Daniel, Trantírek, Lukáš, Mergny, Jean-Louis, Vorlíčková, Michaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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