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Diversity of Parallel Guanine Quadruplexes Induced by Guanine Substitutions
K. Bednářová, M. Vorlíčková, D. Renčiuk
Language English Country Switzerland
Document type Journal Article
Grant support
17-19170Y
Grantová Agentura České Republiky
20-20229S
Grantová Agentura České Republiky
19-17063S
Grantová Agentura České Republiky
CZ.02.1.01/0.0/0.0/15_003/0000477
European Regional Development Fund
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
32854410
DOI
10.3390/ijms21176123
Knihovny.cz E-resources
- MeSH
- Circular Dichroism MeSH
- DNA chemistry genetics MeSH
- G-Quadruplexes MeSH
- Guanine chemistry MeSH
- Nucleic Acid Conformation MeSH
- Models, Molecular MeSH
- Amino Acid Substitution * MeSH
- Thermodynamics MeSH
- Hydrogen Bonding MeSH
- Publication type
- Journal Article MeSH
Recently, we reported an inhibitory effect of guanine substitutions on the conformational switch from antiparallel to parallel quadruplexes (G4) induced by dehydrating agents. As a possible cause, we proposed a difference in the sensitivity of parallel and antiparallel quadruplexes to the guanine substitutions in the resulting thermodynamic stability. Reports on the influence of guanine substitutions on the biophysical properties of intramolecular parallel quadruplexes are rare. Moreover, such reports are often complicated by the multimerisation tendencies of parallel quadruplexes. To address this incomplete knowledge, we employed circular dichroism spectroscopy (CD), both as stopped-flow-assisted fast kinetics measurements and end-point measurements, accompanied by thermodynamic analyses, based on UV absorption melting profiles, and electrophoretic methods. We showed that parallel quadruplexes are significantly more sensitive towards guanine substitutions than antiparallel ones. Furthermore, guanine-substituted variants, which in principle might correspond to native genomic sequences, distinctly differ in their biophysical properties, indicating that the four guanines in each tetrad of parallel quadruplexes are not equal. In addition, we were able to distinguish by CD an intramolecular G4 from intermolecular ones resulting from multimerisation mediated by terminal tetrad association, but not from intermolecular G4s formed due to inter-strand Hoogsteen hydrogen bond formation. In conclusion, our study indicates significant variability in parallel quadruplex structures, otherwise disregarded without detailed experimental analysis.
References provided by Crossref.org
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