DNA i-motif formation at neutral pH is driven by kinetic partitioning

Author:

Školáková Petra1ORCID,Gajarský Martin2,Palacký Jan1ORCID,Šubert Denis13ORCID,Renčiuk Daniel1ORCID,Trantírek Lukáš2ORCID,Mergny Jean-Louis14ORCID,Vorlíčková Michaela1ORCID

Affiliation:

1. Department of Biophysics of Nucleic Acids, Institute of Biophysics of the Czech Academy of Sciences , Královopolská 135, Brno  612 00, Czech Republic

2. Central European Institute of Technology, Masaryk University , Kamenice 5, Brno  625 00, Czech Republic

3. National Centre for Biomolecular Research, Faculty of Science, Masaryk University , Kotlářská 2, Brno  611 37, Czech Republic

4. Laboratoire d’Optique & Biosciences, Institut Polytechnique de Paris , Inserm, CNRS, Ecole Polytechnique, Palaiseau  91128, France

Abstract

AbstractCytosine-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 (CnT3)3Cn (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.

Funder

Czech Science Foundation

SYMBIT

ERDF

ANR

Publisher

Oxford University Press (OUP)

Subject

Genetics

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