Literature DB >> 9733641

Sequence dependence of branch migratory minima.

W Sun1, C Mao, F Liu, N C Seeman.   

Abstract

The Holliday junction is a central intermediate in the process of genetic recombination. The position of its branch-point can relocate through an isomerization known as branch migration. This migration occurs because the branch-point is flanked by homologous symmetry. All attempts at modeling the kinetics of branch migration have relied on the assumption that branch migration minima are sequence-independent. We have tested that assumption here, using a competition assay based on symmetric immobile branched junctions; these are junctions that cannot undergo branch migration, despite the fact that they are flanked by homology. The assay used is predicated on the non-association of strands displaced in the assay; we have tested this assumption, and have performed our experiments under conditions where we know that it is true. We have measured the free energy of relocating a branched junction from a fixed non-homologous sequence to all possible dimeric symmetric sequences. We find that the assumption of sequence-independence is often valid, but that it is not universally true. We find that the flanking sequences can have a marked effect on the free energy measured, both for extensions of symmetry and for reversals of flanking nucleotides. We have varied the temperature in our experiments, and have derived both enthalpies and entropies for the different sequences. The entropies are largely unfavorable, whereas the enthalpies are largely favorable; regardless of the signs of these quantities, we see that this is another system where enthalpy-entropy compensation is operative. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9733641     DOI: 10.1006/jmbi.1998.1991

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  8 in total

1.  Direct evidence for spontaneous branch migration in antiparallel DNA Holliday junctions.

Authors:  R Sha; F Liu; N C Seeman
Journal:  Biochemistry       Date:  2000-09-19       Impact factor: 3.162

2.  The flexibility of DNA double crossover molecules.

Authors:  Phiset Sa-Ardyen; Alexander V Vologodskii; Nadrian C Seeman
Journal:  Biophys J       Date:  2003-06       Impact factor: 4.033

3.  Paranemic crossover DNA: a generalized Holliday structure with applications in nanotechnology.

Authors:  Zhiyong Shen; Hao Yan; Tong Wang; Nadrian C Seeman
Journal:  J Am Chem Soc       Date:  2004-02-18       Impact factor: 15.419

Review 4.  The stacked-X DNA Holliday junction and protein recognition.

Authors:  Patricia A Khuu; Andrea Regier Voth; Franklin A Hays; P Shing Ho
Journal:  J Mol Recognit       Date:  2006 May-Jun       Impact factor: 2.137

5.  Solution formation of Holliday junctions in inverted-repeat DNA sequences.

Authors:  Franklin A Hays; Virgil Schirf; P Shing Ho; Borries Demeler
Journal:  Biochemistry       Date:  2006-02-28       Impact factor: 3.162

6.  Single molecule fluorescence analysis of branch migration of holliday junctions: effect of DNA sequence.

Authors:  Mikhail A Karymov; Alexey Bogdanov; Yuri L Lyubchenko
Journal:  Biophys J       Date:  2008-04-18       Impact factor: 4.033

7.  Formation of Extrachromosomal Circular DNA from Long Terminal Repeats of Retrotransposons in Saccharomyces cerevisiae.

Authors:  Henrik D Møller; Camilla E Larsen; Lance Parsons; Anders Johannes Hansen; Birgitte Regenberg; Tobias Mourier
Journal:  G3 (Bethesda)       Date:  2015-12-17       Impact factor: 3.154

8.  Observing spontaneous branch migration of Holliday junctions one step at a time.

Authors:  Sean A McKinney; Alasdair D J Freeman; David M J Lilley; Taekjip Ha
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-11       Impact factor: 11.205

  8 in total

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