TY - JOUR
T1 - In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
AU - Randall, Graham L.
AU - Zechiedrich, Lynn
AU - Pettitt, B. Montgomery
N1 - Funding Information:
We thank Dr John F. Marko for helpful discussion and advice and Dr Jonathan M. Fogg for critically reading the manuscript. The computations were performed in part using the Teragrid and the Molecular Science Computing Facility in the William R. Wiley Environmental Molecular Sciences Laboratory, sponsored by the US Department of Energy’s Office of Biological and Environmental Research and located at the Pacific Northwest National Laboratory.
Funding Information:
Robert A. Welch Foundation (E-1028 to B.M.P); National Institutes of Health (R01GM066813 to B.M.P., R01AI054830 to L.Z.); Keck Center for Interdisciplinary Bioscience Training of the Gulf Coast Consortia (National Library of Medicine Grant No. 5T15LM07093 to G.L.R.).
PY - 2009/7/8
Y1 - 2009/7/8
N2 - To understand how underwinding and overwinding the DNA helix affects its structure, we simulated 19 independent DNA systems with fixed degrees of twist using molecular dynamics in a system that does not allow writhe. Underwinding DNA induced spontaneous, sequence-dependent base flipping and local denaturation, while overwinding DNA induced the formation of Pauling-like DNA (P-DNA). The winding resulted in a bimodal state simultaneously including local structural failure and B-form DNA for both underwinding and extreme overwinding. Our simulations suggest that base flipping and local denaturation may provide a landscape influencing protein recognition of DNA sequence to affect, for examples, replication, transcription and recombination. Additionally, our findings help explain results from single-molecule experiments and demonstrate that elastic rod models are strictly valid on average only for unstressed or overwound DNA up to P-DNA formation. Finally, our data support a model in which base flipping can result from torsional stress.
AB - To understand how underwinding and overwinding the DNA helix affects its structure, we simulated 19 independent DNA systems with fixed degrees of twist using molecular dynamics in a system that does not allow writhe. Underwinding DNA induced spontaneous, sequence-dependent base flipping and local denaturation, while overwinding DNA induced the formation of Pauling-like DNA (P-DNA). The winding resulted in a bimodal state simultaneously including local structural failure and B-form DNA for both underwinding and extreme overwinding. Our simulations suggest that base flipping and local denaturation may provide a landscape influencing protein recognition of DNA sequence to affect, for examples, replication, transcription and recombination. Additionally, our findings help explain results from single-molecule experiments and demonstrate that elastic rod models are strictly valid on average only for unstressed or overwound DNA up to P-DNA formation. Finally, our data support a model in which base flipping can result from torsional stress.
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U2 - 10.1093/nar/gkp556
DO - 10.1093/nar/gkp556
M3 - Article
C2 - 19586933
AN - SCOPUS:70449711324
SN - 0305-1048
VL - 37
SP - 5568
EP - 5577
JO - Nucleic acids research
JF - Nucleic acids research
IS - 16
M1 - gkp556
ER -