Transition dynamics and selection of the distinct S-DNA and strand unpeeling modes of double helix overstretching

Hongxia Fu, Hu Chen, Xinghua Zhang, Yuanyuan Qu, John F. Marko, Jie Yan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

79 Scopus citations

Abstract

Recent studies have revealed two distinct pathways for the DNA overstretching transition near 65 pN: 'unpeeling' of one strand from the other, and a transition from B-DNA to an elongated double-stranded 'S-DNA' form. However, basic questions concerning the dynamics of these transitions, relative stability of the two competing overstretched states, and effects of nicks and free DNA ends on overstretching, remain open. In this study we report that: (i) stepwise extension changes caused by sequence-defined barriers occur during the strand-unpeeling transition, whereas rapid, sequence-independent extension fluctuations occur during the B to S transition; (ii) the secondary transition that often occurs following the overstretching transition is strand-unpeeling, during which the extension increases by 0.01-0.02nm per base pair of S-DNA converted to single-stranded DNA at forces between 75 and 110 pN; (iii) even in the presence of nicks or free ends, S-DNA can be stable under physiological solution conditions; (iv) distribution of small GC-rich islands in a large DNA plays a key role in determining the transition pathways; and (v) in the absence of nicks or free ends, torsion-unconstrained DNA undergoes the overstretching transition via creation of S-DNA. Our study provides a new, high-resolution understanding of the competition between unpeeling and formation of S-DNA.

Original languageEnglish (US)
Pages (from-to)3473-3481
Number of pages9
JournalNucleic acids research
Volume39
Issue number8
DOIs
StatePublished - Apr 2011

Funding

Ministry of Education of Singapore, NUS (grants R144000192112 and R144000251112); Mechanobiology Institute at National University of Singapore; Singapore-MIT Alliance for Research and Technology at National University of Singapore; National Science Foundation, NU (grants DMR-0520513, DMR-0715099 and PHY-0852130); National Institutes of Health-National Cancer Institute (grant U54-CA143869-01); Chicago Biomedical Consortium with support from The Searle Funds at The Chicago Community Trust. Funding for open access charge: Mechanobiology Institute at National University of Singapore.

ASJC Scopus subject areas

  • Genetics

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