DNA Quadruplex Structure with a Unique Cation Dependency

Author:

Gajarsky Martin12ORCID,Stadlbauer Petr3ORCID,Sponer Jiri3ORCID,Cucchiarini Anne14,Dobrovolna Michaela35,Brazda Vaclav35ORCID,Mergny Jean‐Louis34ORCID,Trantirek Lukas1ORCID,Lenarcic Zivkovic Martina16ORCID

Affiliation:

1. Central European Institute of Technology (CEITEC) Masaryk University Kamenice 753/5 62500 Brno Czech Republic

2. Current address: Center for Molecular Medicine Cologne University of Cologne 50931 Cologne Germany

3. Institute of Biophysics Czech Academy of Sciences Kralovopolska 135 61265 Brno Czech Republic

4. Laboratoire d'Optique et Biosciences Ecole Polytechnique CNRS Inserm Institut Polytechnique de Paris 91120 Palaiseau France

5. Faculty of Chemistry Brno University of Technology Purkynova 464 61200 Brno Czech Republic

6. Slovenian NMR Centre National Institute of Chemistry Hajdrihova 19 1000 Ljubljana Slovenia

Abstract

AbstractDNA quadruplex structures provide an additional layer of regulatory control in genome maintenance and gene expression and are widely used in nanotechnology. We report the discovery of an unprecedented tetrastranded structure formed from a native G‐rich DNA sequence originating from the telomeric region of Caenorhabditis elegans. The structure is defined by multiple properties that distinguish it from all other known DNA quadruplexes. Most notably, the formation of a stable so‐called KNa‐quadruplex (KNaQ) requires concurrent coordination of K+ and Na+ ions at two distinct binding sites. This structure provides novel insight into G‐rich DNA folding under ionic conditions relevant to eukaryotic cell physiology and the structural evolution of telomeric DNA. It highlights the differences between the structural organization of human and nematode telomeric DNA, which should be considered when using C. elegans as a model in telomere biology, particularly in drug screening applications. Additionally, the absence/presence of KNaQ motifs in the host/parasite introduces an intriguing possibility of exploiting the KNaQ fold as a plausible antiparasitic drug target. The structure's unique shape and ion dependency and the possibility of controlling its folding by using low‐molecular‐weight ligands can be used for the design or discovery of novel recognition DNA elements and sensors.

Funder

Grantová Agentura České Republiky

Ministerstvo Školství, Mládeže a Tělovýchovy

Publisher

Wiley

Subject

General Medicine

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