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Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands

By substitution of natural nucleotides by their abasic analogs (i.e., 1′,2′-dideoxyribose phosphate residue) at critically chosen positions within 27-bp DNA constructs originating from the first intron of N-myc gene, we hindered hybridization within the guanine- and cytosine-rich central region and...

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Autores principales: Trajkovski, Marko, Plavec, Janez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037129/
https://www.ncbi.nlm.nih.gov/pubmed/31972988
http://dx.doi.org/10.3390/molecules25030434
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author Trajkovski, Marko
Plavec, Janez
author_facet Trajkovski, Marko
Plavec, Janez
author_sort Trajkovski, Marko
collection PubMed
description By substitution of natural nucleotides by their abasic analogs (i.e., 1′,2′-dideoxyribose phosphate residue) at critically chosen positions within 27-bp DNA constructs originating from the first intron of N-myc gene, we hindered hybridization within the guanine- and cytosine-rich central region and followed formation of non-canonical structures. The impeded hybridization between the complementary strands leads to time-dependent structural transformations of guanine-rich strand that are herein characterized with the use of solution-state NMR, CD spectroscopy, and native polyacrylamide gel electrophoresis. Moreover, the DNA structural changes involve transformation of intra- into inter-molecular G-quadruplex structures that are thermodynamically favored. Intriguingly, the transition occurs in the presence of complementary cytosine-rich strands highlighting the inability of Watson–Crick base-pairing to preclude the transformation between G-quadruplex structures that occurs via intertwining mechanism and corroborates a role of G-quadruplex structures in DNA recombination processes.
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spelling pubmed-70371292020-03-11 Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands Trajkovski, Marko Plavec, Janez Molecules Article By substitution of natural nucleotides by their abasic analogs (i.e., 1′,2′-dideoxyribose phosphate residue) at critically chosen positions within 27-bp DNA constructs originating from the first intron of N-myc gene, we hindered hybridization within the guanine- and cytosine-rich central region and followed formation of non-canonical structures. The impeded hybridization between the complementary strands leads to time-dependent structural transformations of guanine-rich strand that are herein characterized with the use of solution-state NMR, CD spectroscopy, and native polyacrylamide gel electrophoresis. Moreover, the DNA structural changes involve transformation of intra- into inter-molecular G-quadruplex structures that are thermodynamically favored. Intriguingly, the transition occurs in the presence of complementary cytosine-rich strands highlighting the inability of Watson–Crick base-pairing to preclude the transformation between G-quadruplex structures that occurs via intertwining mechanism and corroborates a role of G-quadruplex structures in DNA recombination processes. MDPI 2020-01-21 /pmc/articles/PMC7037129/ /pubmed/31972988 http://dx.doi.org/10.3390/molecules25030434 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Trajkovski, Marko
Plavec, Janez
Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title_full Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title_fullStr Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title_full_unstemmed Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title_short Chasing Particularities of Guanine- and Cytosine-Rich DNA Strands
title_sort chasing particularities of guanine- and cytosine-rich dna strands
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037129/
https://www.ncbi.nlm.nih.gov/pubmed/31972988
http://dx.doi.org/10.3390/molecules25030434
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