Journal article
DNA cruciform arms nucleate through a correlated but asynchronous cooperative mechanism.
- Abstract:
- Inverted repeat (IR) sequences in DNA can form noncanonical cruciform structures to relieve torsional stress. We use Monte Carlo simulations of a recently developed coarse-grained model of DNA to demonstrate that the nucleation of a cruciform can proceed through a cooperative mechanism. First, a twist-induced denaturation bubble must diffuse so that its midpoint is near the center of symmetry of the IR sequence. Second, bubble fluctuations must be large enough to allow one of the arms to form a small number of hairpin bonds. Once the first arm is partially formed, the second arm can rapidly grow to a similar size. Because bubbles can twist back on themselves, they need considerably fewer bases to resolve torsional stress than the final cruciform state does. The initially stabilized cruciform therefore continues to grow, which typically proceeds synchronously, reminiscent of the S-type mechanism of cruciform formation. By using umbrella sampling techniques, we calculate, for different temperatures and superhelical densities, the free energy as a function of the number of bonds in each cruciform arm along the correlated but asynchronous nucleation pathways we observed in direct simulations.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Authors
- Publisher:
- American Chemical Society
- Journal:
- journal of physical chemistry. B More from this journal
- Volume:
- 116
- Issue:
- 38
- Pages:
- 11616-11625
- Publication date:
- 2012-09-01
- DOI:
- EISSN:
-
1520-5207
- ISSN:
-
1520-6106
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:340086
- UUID:
-
uuid:d5cd8424-1153-42e9-b65a-a85f0a405375
- Local pid:
-
pubs:340086
- Source identifiers:
-
340086
- Deposit date:
-
2013-03-20
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2012
- Notes:
-
Copyright © 2012 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in
Journal of Physical Chemistry B, copyright © American Chemical Society after peer review and technical editing by the publisher.
To access the final edited and published work see [insert ACS Articles on Request author-directed link to
Published Work, see http://dx.doi.org/10.1021/jp3080755.
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