The static and dynamic structural heterogeneities of B-DNA: extending Calladine–Dickerson rules

Author:

Dans Pablo D12ORCID,Balaceanu Alexandra1,Pasi Marco34,Patelli Alessandro S5,Petkevičiūtė Daiva56,Walther Jürgen1ORCID,Hospital Adam1,Bayarri Genís1,Lavery Richard4,Maddocks John H5,Orozco Modesto17

Affiliation:

1. Institute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology. Baldiri Reixac 10–12, 08028 Barcelona, Spain

2. Department of Biological Sciences, University of the Republic (UdelaR), CENUR Gral. Rivera 1350, 50000 Salto, Uruguay

3. LBPA, École normale supérieure Paris-Saclay, 61 Av. du Pdt Wilson, Cachan 94235, France

4. Bases Moléculaires et Structurales des Systèmes Infectieux, Univ. Lyon I/CNRS UMR 5086, IBCP, 7 Passage du Vercors, Lyon 69367, France

5. Institute of Mathematics, Swiss Federal Institute of Technology (EPFL), CH-1015 Lausanne, Switzerland

6. Faculty of Mathematics and Natural Sciences, Kaunas University of Technology, Studentų g. 50, 51368 Kaunas, Lithuania

7. Department of Biochemistry and Molecular Biology. University of Barcelona, 08028 Barcelona, Spain

Abstract

AbstractWe present a multi-laboratory effort to describe the structural and dynamical properties of duplex B-DNA under physiological conditions. By processing a large amount of atomistic molecular dynamics simulations, we determine the sequence-dependent structural properties of DNA as expressed in the equilibrium distribution of its stochastic dynamics. Our analysis includes a study of first and second moments of the equilibrium distribution, which can be accurately captured by a harmonic model, but with nonlocal sequence-dependence. We characterize the sequence-dependent choreography of backbone and base movements modulating the non-Gaussian or anharmonic effects manifested in the higher moments of the dynamics of the duplex when sampling the equilibrium distribution. Contrary to prior assumptions, such anharmonic deformations are not rare in DNA and can play a significant role in determining DNA conformation within complexes. Polymorphisms in helical geometries are particularly prevalent for certain tetranucleotide sequence contexts and are always coupled to a complex network of coordinated changes in the backbone. The analysis of our simulations, which contain instances of all tetranucleotide sequences, allow us to extend Calladine–Dickerson rules used for decades to interpret the average geometry of DNA, leading to a set of rules with quantitative predictive power that encompass nonlocal sequence-dependence and anharmonic fluctuations.

Funder

Spanish Ministry of Science

Catalan SGR

Instituto Nacional de Bioinformática

European Research Council

Horizon 2020

Biomolecular & Bioinformatics Resources Platform

Fondo Europeo de Desarrollo Regional

MINECO

CNRS

ANR

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference75 articles.

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