2014
Mechanical properties of symmetric and asymmetric DNA A-tracts: implications for looping and nucleosome positioning
DRSATA, Tomáš, Naďa ŠPAČKOVÁ, Petr JUREČKA, Marie ZGARBOVÁ, Jiří ŠPONER et. al.Základní údaje
Originální název
Mechanical properties of symmetric and asymmetric DNA A-tracts: implications for looping and nucleosome positioning
Autoři
DRSATA, Tomáš (203 Česká republika), Naďa ŠPAČKOVÁ (203 Česká republika), Petr JUREČKA (203 Česká republika), Marie ZGARBOVÁ (203 Česká republika), Jiří ŠPONER (203 Česká republika, garant, domácí) a Filip LANKAŠ (203 Česká republika)
Vydání
Nucleic Acids Research, Oxford, Oxford University Press, 2014, 0305-1048
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10403 Physical chemistry
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 9.112
Kód RIV
RIV/00216224:14740/14:00076810
Organizační jednotka
Středoevropský technologický institut
UT WoS
000338769400055
Klíčová slova anglicky
MOLECULAR-DYNAMICS SIMULATIONS; SEQUENCE-DIRECTED CURVATURE; ADENINE-THYMINE TRACT; BASE-PAIR LEVEL; INDIRECT READOUT; NUCLEIC-ACIDS; B-DNA; CONFORMATIONAL-ANALYSIS; DISFAVORING SEQUENCES; ELASTIC PROPERTIES
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 13. 10. 2014 10:39, Martina Prášilová
Anotace
V originále
A-tracts are functionally important DNA sequences which induce helix bending and have peculiar structural properties. While A-tract structure has been qualitatively well characterized, their mechanical properties remain controversial. A-tracts appear structurally rigid and resist nucleosome formation, but seem flexible in DNA looping. In this work, we investigate mechanical properties of symmetric A(n)T(n) and asymmetric A(2n) tracts for n = 3, 4, 5 using two types of coarse-grained models. The first model represents DNA as an ensemble of interacting rigid bases with non-local quadratic deformation energy, the second one treats DNA as an anisotropically bendable and twistable elastic rod. Parameters for both models are inferred from microsecond long, atomic-resolution molecular dynamics simulations. We find that asymmetric A-tracts are more rigid than the control G/C-rich sequence in localized distortions relevant for nucleosome formation, but are more flexible in global bending and twisting relevant for looping. The symmetric tracts, in contrast, are more rigid than asymmetric tracts and the control, both locally and globally. Our results can reconcile the contradictory stiffness data on A-tracts and suggest symmetric A-tracts to be more efficient in nucleosome exclusion than the asymmetric ones. This would open a new possibility of gene expression manipulation using A-tracts.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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